Impact of Diagnosis-to-Treatment Interval on the Outcome of Patients with Acute Myeloid Leukemia

Impact of Diagnosis-to-Treatment Interval on the Outcome of Patients with Acute Myeloid Leukemia | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Short Report Impact of Diagnosis-to-Treatment Interval on the Outcome of Patients with Acute Myeloid Leukemia Samah Nassereddine, Yuan Feng, Jordan Selep, Firas El Chaer, Leah Wells, and 9 more This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-8147567/v1 This work is licensed under a CC BY 4.0 License Status: Under Review Version 1 posted 9 You are reading this latest preprint version Abstract Background: Acute myeloid leukemia (AML) is considered an oncologic emergency, yet the optimal timing for treatment initiation remains uncertain. Methods: We conducted a multi-institutional retrospective study of 698 adults with newly diagnosed AML presenting to four academic centers across the United States. Diagnosis-to-treatment intervals (DTI) were categorized as 10 days. Outcomes were analyzed using multivariable models adjusting for age, treatment intensity, ELN 2017 risk classification, and white blood cell count. Results: Among younger patients, DTI was not associated with differences in survival outcomes. In contrast, older patients demonstrated improved survival with delayed treatment (DTI >10 days), particularly those with lower white blood cell counts. No adverse effects from treatment delay were observed in younger cohorts. Conclusions: This retrospective study has showed that prolonged DTI is associated with improved survival in older adults with newly diagnosed AML, challenging the traditional assumption that immediate therapy universally improves outcomes. These findings underscore the importance of individualized treatment timing in the era of precision oncology. Acute myeloid leukemia diagnosis-to-treatment interval induction chemotherapy molecular testing risk stratification targeted therapy precision medicine treatment outcomes Figures Figure 1 Figure 2 Introduction The diagnosis of acute myeloid leukemia (AML) is an oncologic emergency that often necessitates prompt initiation of therapy. The optimal timing of therapy initiation has long been debated, and current guidelines do not provide specific recommendations regarding the diagnosis-to-treatment interval (DTI) in patients with AML. Historically, prompt initiation of induction chemotherapy was considered crucial to mitigate disease-related morbidity and mortality, particularly among younger patients with proliferative AML. 1 However, with the 2017 and 2022 revisions of the World Health Organization (WHO) and International Consensus Classification (ICC) systems, molecular characterization has become increasingly integral to AML diagnosis and risk stratification. 2 , 3 Moreover, the expanding molecular landscape of AML also informs therapeutic decision-making and disease monitoring. 4 Over the past decade, the introduction of targeted therapies for actionable mutations has transformed AML management, underscoring the growing importance of genomic profiling in guiding treatment decisions and improving clinical outcomes. 4 , 5 , 6 , 7 , 8 The BEAT AML Master clinical trial, the first prospective precision medicine trial in hematologic malignancies, demonstrated superior outcomes when patients with actionable mutations received targeted therapy rather than standard of care. In addition, delaying therapy to await molecular testing results was found to be safe in patients without evidence of hyperleukocytosis. 9 In routine practice, however, the turnaround time for comprehensive molecular profiling can be prolonged, typically requiring 7 to 14 days for completion. Although enrollment in clinical trials may expedite access to results and targeted agents, most patients are treated in real-world settings with standard of care regimens. 10 To address the clinical uncertainty surrounding the timing of therapy initiation, we conducted a multi-institutional retrospective study across four U.S. academic centers to address the impact of DTI on outcomes in newly diagnosed AML. Our study aimed to define the optimal treatment window in the contemporary era of precision oncology, where molecular testing increasingly guides therapeutic selection and clinical decision-making. Methods We retrospectively collected data on 698 adult patients (aged ≥ 18 years) with newly diagnosed AML treated at four academic cancer centers between 2010 to 2021: the GW Cancer Center, Georgetown University Hospital, University of Virginia, and University of Washington/Fred Hutchinson Cancer Center. Patients with acute promyelocytic leukemia and those who elected to receive treatment at other institutions were excluded. Baseline demographic and clinical characteristics were obtained through detailed chart review and included age, sex, race, smoking status, comorbidities, and disease characteristics such as presenting white blood cell (WBC) count, bone marrow morphology, cytogenetic and fluorescence in situ hybridization (FISH) results, and next-generation sequencing (NGS) findings when available. Treatment-related variables included regimen intensity (low vs. high) and time from diagnosis to therapy initiation. Low-intensity therapy was defined as treatment with a hypomethylating agent (HMA) alone, HMA combined with venetoclax, or low-dose cytarabine (LoDAC) with or without venetoclax. High-intensity therapy was defined as conventional intensive induction chemotherapy (i.e., “7 + 3” or a high-dose cytarabine containing regimen). Institutional review board approval and data-sharing agreements were obtained at all participating sites. The primary outcome was overall survival (OS), defined as the time from AML diagnosis to death from any cause or last follow-up for censored patients. Patients were categorized into three DTI groups: less than five days ( 10). A landmark analysis was performed to evaluate the association between DTI category and OS and to mitigate immortal time bias. Patients who died or were censored within the first 10 days of diagnosis were excluded. For the remaining cohort, survival time was calculated beginning on day 10 post-diagnosis (landmark time). Cox proportional hazards regression models were used to evaluate the association between DTI and OS. The 65 years), baseline WBC count (≤ 100 × 10 9 /L vs. >100 × 10 9 /L), 2017 European Leukemia Net (ELN) risk category (favorable, intermediate, or adverse), and treatment intensity (high vs. low). Interaction terms between DTI and both age and WBC categories were included in to assess whether the effect of DTI on OS differed across subgroups. Hazard ratios (HRs) with corresponding 95% confidence intervals (CIs) were estimated for all comparisons. Linear contrasts of model coefficients were constructed to derive HRs and 95% CIs for specific subgroup analyses (DTI effects within age or WBC strata and pairwise comparisons between non-reference DTI categories. Confidence intervals were calculated using the Delta method, with log-transformed limits subsequently exponentiated. The proportional hazards assumption was verified by examining the Schoenfeld residuals and associated plots, with no significant violations observed. For analyses involving multiple contrasts, p-values were adjusted using the single-step method based on the multivariate normal distribution of contrasts to control the family-wise error rate. All analyses were performed using the R Statistical Software (version v4.4.2; R Core Team, 2024). Survival analyses were conducted using the survival package, and multiple comparison adjustments were implemented using the multcomp package. A two-sided p-value < 0.05 was considered statistically significant. Results A total of 698 patients across four academic centers were included in the analysis assessing the impact of the DTI on outcomes in AML. Patients were categorized into three DTI groups: 10 days (n = 257). Baseline characteristics are summarized in Table 1 . Patients with delayed therapy (> 10 days) were older (median 66.0 years, interquartile range [IQR] 57–74) compared with those treated within 1–5 days (median 60.5 years, IQR 49–70) and presented with lower white blood cell (WBC) counts (mean 15.0 vs. 52.9 ×10³/µL). Elevated WBC counts (> 100 ×10³/µL) were most common among those treated within five days (19.1%). Adverse ELN risk was more frequent in the > 10-day group (46.7%) than in the < 1–5-day group (38.3%, Fisher's exact test, p = 0.005). High-intensity induction therapy was more often administered to patients with early DTI (77.5% for 10 days; Fisher's exact test, p < 0.001). Kaplan–Meier survival curves demonstrated substantial overlap across DTI categories, with no significant difference by log-rank test (p = 0.982; WBC ≤ 100 × 10³/µL subgroup p = 0.949) (Fig. 1). Similarly, unadjusted Cox analyses revealed no significant association between DTI and OS, with HRs near 1 for both the 6–10 day and > 10-day groups relative to the 10 days) was associated with improved survival, corresponding to a 32% reduction in mortality risk compared with early treatment (HR 0.68, 95% CI: 0.53–0.87, p = 0.003). Subgroup analyses ( Table 3 ) revelated that this benefit was most pronounced among older patients (> 65 years) with WBC ≤ 100 ×10³/µL, in whom a DTI > 10 days conferred a 38% lower mortality risk compared with treatment within five days (HR 0.62, 95% CI: 0.39–0.99, adjusted p = 0.040). Within this same subgroup, outcomes were also superior for patients treated after > 10 days compared with those treated within 6–10 days (HR 0.53, 95% CI: 0.30–0.95, adjusted p = 0.024). No significant survival differences by DTI were observed among younger patients (≤ 65 years) or among those with WBC > 100 ×10³/µL after adjustment for covariates. Independent of DTI, several factors were significantly associated with survival. Adverse predictors included older age (per year; HR 1.03, 95% CI 1.02–1.04), higher WBC count (per 10³/µL; HR 1.002, 95% CI 1.001–1.004), intermediate ELN risk (HR 1.70, 95% CI 1.22–2.37), adverse ELN risk (HR 2.12, 95% CI 1.54–2.94), and low-intensity therapy vs high-intensity (HR 1.64, 95% CI 1.27–2.13) (Table 2) . These associations were similar in interaction models, with older age (> 65 vs ≤ 65) (HR 2.14, 95% CI 1.54–2.98), intermediate ELN risk (HR 1.76, 95% CI 1.26–2.46), adverse ELN risk (HR 2.20, 95% CI 1.59–3.05), and low-intensity therapy (HR 1.81, 95% CI 1.41–2.31) continuing to predict inferior outcomes (Table 4) . The only factor independently associated with improved OS was a prolonged DTI > 10 days, an effect restricted to older patients with lower WBC counts, as noted above. The proportional hazards assumption was assessed with Schoenfeld residuals. Although the global test approached significance (p = 0.049), the assumption held for the DTI variable (p = 0.332), corroborated by residual plots showing no systematic deviation (Fig. 2). Discussion Our findings reveal an unexpected association between the DTI and outcomes in older patients with AML. Specifically, prolonged DTI was associated with reduced mortality in older patients, whereas no survival benefit was observed in younger patients. Even among young patients with elevated WBC counts, treatment delay did not significantly influence outcomes. This observation differentiates our analysis from prior large registry studies, such as the German Study Alliance Leukemia–Acute Myeloid Leukemia (SAL-AML) and TriNetX registry or reports by Röllig et al. and Bertolli et al, which found no significant impact of DTI on survival. 11 , 12 , 13 Another large retrospective study of 1,317 patients from the Cleveland Clinic and the MD Anderson Cancer Center reported lower complete response (CR) and OS rates among young patients when DTI exceeded five days, while outcomes among older patients remained unaffected. 6 Similarly, an ECOG study of 362 patients demonstrated lower CR rates with delayed therapy initiation, although this did not translate into an OS difference. 13 Evaluating the effect of DTI is inherently complex due to selection bias inherent to retrospective study designs. To mitigate this bias, we stratified patients by WBC count. Interestingly, even in patients with hyperleukocytosis, prolonged DTI did not adversely influence outcomes. Other potential confounders, such as disseminated intravascular coagulopathy (DIC), active infection/ or sepsis, and transfusion requirements, may also have contributed to differences in early mortality and treatment tolerance. To our knowledge, this is the first study to demonstrate a potential adverse impact of shorter DTI in older patients with AML. Several explanations may account for this finding. AML is a biologically and clinically heterogeneous disease, and older patients who received therapy earlier may have presented with greater clinical instability or more aggressive disease features, prompting expedited treatment initiation. Such patients may also have been less physiologically fit, predisposing them to treatment-related complications and early mortality. Our dataset did not capture clinical parameters such as infection or DIC, which limits our ability to test this hypothesis directly. Furthermore, our cohort largely predated the widespread use of venetoclax-based regimens, which may limit applicability to contemporary treatment paradigms. 14 Given these considerations, our results should be regarded as hypothesis-generating rather than definitive evidence of causality. Notably, prior studies examining DTI in AML have employed heterogeneous definitions of “delay”, with intervals varying widely across analyses. Some modeled DTI as a continuous variable, while others used categorical thresholds, as in our study. A prior meta-analysis suggested that median DTI across studies typically ranged from four to eight days. 15 Our study has several limitations. First, its retrospective design introduces potential selection bias and confounding by indication, as patients perceived to be more acutely ill were likely prioritized for earlier treatment. Second, the landmark analysis, while essential to minimize immortal time bias, inherently excluded patients who died within 10 days of diagnosis, thereby limiting generalizability to early survivors. Third, data granularity was constrained: precise treatment initiation dates were unavailable, necessitating calculating of OS from the date of diagnosis rather than from the start of therapy. This approach, although standard, reflects the full disease trajectory rather than isolating post-treatment survival. Conclusion In this multi-institutional retrospective study, a prolonged diagnosis-to-treatment interval was associated with improved survival among older patients with newly diagnosed AML, particularly those with lower white blood cell counts, while no adverse effect of treatment delay was observed in younger patients. These findings challenge the traditional assumption that immediate initiation of therapy universally improves outcomes and underscore the importance of individualized treatment timing in the era of precision oncology. Prospective studies are warranted to validate these results and to determine whether a brief delay to obtain comprehensive molecular data and optimize therapeutic selection may improve outcomes in clinically stable patients. Declarations Acknowledgments: The authors used an artificial intelligence-based tool for scholarly writing, specifically “Paperpal,” to assist with refining the English language and improving writing quality. No AI tools were used to summarize the content or any other form of writing. The authors take full responsibility for the content of this manuscript. There was no funding associated with this paper. Conflict of Interest: FEC reports Consultant: SPD Oncology, Amgen, CTI BioPharma, AbbVie, MorphoSys, PharmaEssentia, BMS, Geron, Sobi, DAVA Oncology, Taiho Oncology, Daiichi Sankyo, Syndax, Novartis, Merck. CL does consulting for AbbVie, Astellas, Arcellx, Syndax, Kura, Rigel, Stemline, Geron, Daiichi, and BMS, and has research funding from Jazz Pharma and BMS. MEP has research funding to her institution from Abbvie, Ascentage, Astex, Oncoverity, and Pfizer Authors contributions: SN, FEC, IT, MEP and CL contributed to study conception and design. Material preparation, data collection and analysis were performed by Samah Nassereddine, Vanyal Aggarwal, Kimberly Doucette, Lacy Williams, Leah Wells, Ramy Elsarrag, Jordan Selep, Yuan Feng, and Shanshan Liu, Guoquing Diao. The first draft of the manuscript was written by Samah Nassereddine and all authors commented on previous versions of the manuscript. Ethics and Consent to Participate declarations: not applicable References Sekeres MA, Elson P, Kalaycio ME et al (2009) Time from diagnosis to treatment initiation predicts survival in younger, but not older, acute myeloid leukemia patients. Blood 113(1):2836. 10.1182/blood200805157065 Arber DA, Orazi A, Hasserjian R et al (2022) International Consensus Classification of Myeloid Neoplasms and Acute Leukemia: integrating morphologic, clinical, and genomic data. Blood 140(11):1200–1228. 10.1182/blood.2022012382 Khoury JD, Solary E, Abla O et al (2022) The 5th edition of the World Health Organization classification of haematolymphoid tumours: myeloid and histiocytic/dendritic neoplasms. 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J Clin Oncol 29(33):4417–4423. 10.1200/JCO.2011.35.7525 Tables Tables 1 to 4 are available in the Supplementary Files section. Additional Declarations No competing interests reported. Supplementary Files Table1.jpg Table2.jpg Table3.jpg Table4.jpg Cite Share Download PDF Status: Under Review Version 1 posted Editorial decision: Revision requested 24 Jan, 2026 Reviews received at journal 04 Jan, 2026 Reviews received at journal 01 Jan, 2026 Reviewers agreed at journal 09 Dec, 2025 Reviewers agreed at journal 06 Dec, 2025 Reviewers invited by journal 04 Dec, 2025 Editor assigned by journal 27 Nov, 2025 Submission checks completed at journal 27 Nov, 2025 First submitted to journal 18 Nov, 2025 You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. 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1","display":"","copyAsset":false,"role":"figure","size":101001,"visible":true,"origin":"","legend":"\u003cp\u003eSee image above for figure legend\u003c/p\u003e","description":"","filename":"Figure11.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8147567/v1/0bddf16b83aa11ddf979ab06.jpg"},{"id":97705812,"identity":"63397b88-3eed-419a-93ed-896a1ae5432b","added_by":"auto","created_at":"2025-12-08 12:54:13","extension":"jpg","order_by":2,"title":"Figure 2","display":"","copyAsset":false,"role":"figure","size":214962,"visible":true,"origin":"","legend":"\u003cp\u003eSee image above for figure legend\u003c/p\u003e","description":"","filename":"Figure2.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8147567/v1/06f2a5e9b3ba13591a61813d.jpg"},{"id":98622310,"identity":"36b16975-2bed-4d64-a79a-3f8a9506d1fa","added_by":"auto","created_at":"2025-12-19 16:51:44","extension":"pdf","order_by":0,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":788653,"visible":true,"origin":"","legend":"","description":"","filename":"manuscript.pdf","url":"https://assets-eu.researchsquare.com/files/rs-8147567/v1/8a3db83a-1333-4307-8390-ded7bbd6025f.pdf"},{"id":97705961,"identity":"49a8589b-7d4d-4c2e-ab9e-7060a4a5a7b4","added_by":"auto","created_at":"2025-12-08 12:54:24","extension":"jpg","order_by":0,"title":"","display":"","copyAsset":false,"role":"supplement","size":264465,"visible":true,"origin":"","legend":"","description":"","filename":"Table1.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8147567/v1/c15f753dc655dbcb3db9892e.jpg"},{"id":97705785,"identity":"5cfa470d-e484-4386-8ccf-dad85fd5bdb6","added_by":"auto","created_at":"2025-12-08 12:54:09","extension":"jpg","order_by":1,"title":"","display":"","copyAsset":false,"role":"supplement","size":141357,"visible":true,"origin":"","legend":"","description":"","filename":"Table2.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8147567/v1/4718e54c3ee94be80c16e920.jpg"},{"id":97705960,"identity":"c72f26fa-fc26-4d31-98ad-5412041d319d","added_by":"auto","created_at":"2025-12-08 12:54:24","extension":"jpg","order_by":2,"title":"","display":"","copyAsset":false,"role":"supplement","size":213783,"visible":true,"origin":"","legend":"","description":"","filename":"Table3.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8147567/v1/7abc0e7f4a5343e2d0764977.jpg"},{"id":97705908,"identity":"45d0d9df-3549-44e4-862a-022c4ff84528","added_by":"auto","created_at":"2025-12-08 12:54:16","extension":"jpg","order_by":3,"title":"","display":"","copyAsset":false,"role":"supplement","size":173061,"visible":true,"origin":"","legend":"","description":"","filename":"Table4.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8147567/v1/6427c223fd9eff3ded396955.jpg"}],"financialInterests":"No competing interests reported.","formattedTitle":"Impact of Diagnosis-to-Treatment Interval on the Outcome of Patients with Acute Myeloid Leukemia","fulltext":[{"header":"Introduction","content":"\u003cp\u003eThe diagnosis of acute myeloid leukemia (AML) is an oncologic emergency that often necessitates prompt initiation of therapy. The optimal timing of therapy initiation has long been debated, and current guidelines do not provide specific recommendations regarding the diagnosis-to-treatment interval (DTI) in patients with AML.\u003c/p\u003e\u003cp\u003eHistorically, prompt initiation of induction chemotherapy was considered crucial to mitigate disease-related morbidity and mortality, particularly among younger patients with proliferative AML.\u003csup\u003e\u003cspan citationid=\"CR1\" class=\"CitationRef\"\u003e1\u003c/span\u003e\u003c/sup\u003e However, with the 2017 and 2022 revisions of the World Health Organization (WHO) and International Consensus Classification (ICC) systems, molecular characterization has become increasingly integral to AML diagnosis and risk stratification.\u003csup\u003e\u003cspan citationid=\"CR2\" class=\"CitationRef\"\u003e2\u003c/span\u003e,\u003cspan citationid=\"CR3\" class=\"CitationRef\"\u003e3\u003c/span\u003e\u003c/sup\u003e Moreover, the expanding molecular landscape of AML also informs therapeutic decision-making and disease monitoring.\u003csup\u003e\u003cspan citationid=\"CR4\" class=\"CitationRef\"\u003e4\u003c/span\u003e\u003c/sup\u003e Over the past decade, the introduction of targeted therapies for actionable mutations has transformed AML management, underscoring the growing importance of genomic profiling in guiding treatment decisions and improving clinical outcomes.\u003csup\u003e\u003cspan citationid=\"CR4\" class=\"CitationRef\"\u003e4\u003c/span\u003e,\u003cspan citationid=\"CR5\" class=\"CitationRef\"\u003e5\u003c/span\u003e,\u003cspan citationid=\"CR6\" class=\"CitationRef\"\u003e6\u003c/span\u003e,\u003cspan citationid=\"CR7\" class=\"CitationRef\"\u003e7\u003c/span\u003e,\u003cspan citationid=\"CR8\" class=\"CitationRef\"\u003e8\u003c/span\u003e\u003c/sup\u003e\u003c/p\u003e\u003cp\u003eThe BEAT AML Master clinical trial, the first prospective precision medicine trial in hematologic malignancies, demonstrated superior outcomes when patients with actionable mutations received targeted therapy rather than standard of care. In addition, delaying therapy to await molecular testing results was found to be safe in patients without evidence of hyperleukocytosis.\u003csup\u003e\u003cspan citationid=\"CR9\" class=\"CitationRef\"\u003e9\u003c/span\u003e\u003c/sup\u003e\u003c/p\u003e\u003cp\u003eIn routine practice, however, the turnaround time for comprehensive molecular profiling can be prolonged, typically requiring 7 to 14 days for completion. Although enrollment in clinical trials may expedite access to results and targeted agents, most patients are treated in real-world settings with standard of care regimens.\u003csup\u003e\u003cspan citationid=\"CR10\" class=\"CitationRef\"\u003e10\u003c/span\u003e\u003c/sup\u003e\u003c/p\u003e\u003cp\u003eTo address the clinical uncertainty surrounding the timing of therapy initiation, we conducted a multi-institutional retrospective study across four U.S. academic centers to address the impact of DTI on outcomes in newly diagnosed AML. Our study aimed to define the optimal treatment window in the contemporary era of precision oncology, where molecular testing increasingly guides therapeutic selection and clinical decision-making.\u003c/p\u003e"},{"header":"Methods","content":"\u003cp\u003eWe retrospectively collected data on 698 adult patients (aged\u0026thinsp;\u0026ge;\u0026thinsp;18 years) with newly diagnosed AML treated at four academic cancer centers between 2010 to 2021: the GW Cancer Center, Georgetown University Hospital, University of Virginia, and University of Washington/Fred Hutchinson Cancer Center. Patients with acute promyelocytic leukemia and those who elected to receive treatment at other institutions were excluded. Baseline demographic and clinical characteristics were obtained through detailed chart review and included age, sex, race, smoking status, comorbidities, and disease characteristics such as presenting white blood cell (WBC) count, bone marrow morphology, cytogenetic and fluorescence in situ hybridization (FISH) results, and next-generation sequencing (NGS) findings when available. Treatment-related variables included regimen intensity (low vs. high) and time from diagnosis to therapy initiation. Low-intensity therapy was defined as treatment with a hypomethylating agent (HMA) alone, HMA combined with venetoclax, or low-dose cytarabine (LoDAC) with or without venetoclax. High-intensity therapy was defined as conventional intensive induction chemotherapy (i.e., \u0026ldquo;7\u0026thinsp;+\u0026thinsp;3\u0026rdquo; or a high-dose cytarabine containing regimen). Institutional review board approval and data-sharing agreements were obtained at all participating sites.\u003c/p\u003e\u003cp\u003eThe primary outcome was overall survival (OS), defined as the time from AML diagnosis to death from any cause or last follow-up for censored patients. Patients were categorized into three DTI groups: less than five days (\u0026lt;\u0026thinsp;1\u0026ndash;5), six to ten days (6\u0026ndash;10), and more than ten days (\u0026gt;\u0026thinsp;10).\u003c/p\u003e\u003cp\u003eA landmark analysis was performed to evaluate the association between DTI category and OS and to mitigate immortal time bias. Patients who died or were censored within the first 10 days of diagnosis were excluded. For the remaining cohort, survival time was calculated beginning on day 10 post-diagnosis (landmark time).\u003c/p\u003e\u003cp\u003eCox proportional hazards regression models were used to evaluate the association between DTI and OS. The \u0026lt;\u0026thinsp;1\u0026ndash;5 day category served as the reference group. Multivariable models were adjusted for clinically relevant covariates, including age (\u0026le;\u0026thinsp;65 vs. \u0026gt;65 years), baseline WBC count (\u0026le;\u0026thinsp;100 \u0026times; 10\u003csup\u003e9\u003c/sup\u003e/L vs. \u0026gt;100 \u0026times; 10\u003csup\u003e9\u003c/sup\u003e/L), 2017 European Leukemia Net (ELN) risk category (favorable, intermediate, or adverse), and treatment intensity (high vs. low). Interaction terms between DTI and both age and WBC categories were included in to assess whether the effect of DTI on OS differed across subgroups.\u003c/p\u003e\u003cp\u003eHazard ratios (HRs) with corresponding 95% confidence intervals (CIs) were estimated for all comparisons. Linear contrasts of model coefficients were constructed to derive HRs and 95% CIs for specific subgroup analyses (DTI effects within age or WBC strata and pairwise comparisons between non-reference DTI categories. Confidence intervals were calculated using the Delta method, with log-transformed limits subsequently exponentiated. The proportional hazards assumption was verified by examining the Schoenfeld residuals and associated plots, with no significant violations observed. For analyses involving multiple contrasts, p-values were adjusted using the single-step method based on the multivariate normal distribution of contrasts to control the family-wise error rate. All analyses were performed using the R Statistical Software (version v4.4.2; R Core Team, 2024). Survival analyses were conducted using the \u003cem\u003esurvival\u003c/em\u003e package, and multiple comparison adjustments were implemented using the \u003cem\u003emultcomp\u003c/em\u003e package. A two-sided p-value\u0026thinsp;\u0026lt;\u0026thinsp;0.05 was considered statistically significant.\u003c/p\u003e"},{"header":"Results","content":"\u003cp\u003eA total of 698 patients across four academic centers were included in the analysis assessing the impact of the DTI on outcomes in AML. Patients were categorized into three DTI groups: \u0026lt;1\u0026ndash;5 days (n\u0026thinsp;=\u0026thinsp;324), 6\u0026ndash;10 days (n\u0026thinsp;=\u0026thinsp;117), and \u0026gt;\u0026thinsp;10 days (n\u0026thinsp;=\u0026thinsp;257). Baseline characteristics are summarized in \u003cb\u003eTable\u0026nbsp;1\u003c/b\u003e. Patients with delayed therapy (\u0026gt;\u0026thinsp;10 days) were older (median 66.0 years, interquartile range [IQR] 57\u0026ndash;74) compared with those treated within 1\u0026ndash;5 days (median 60.5 years, IQR 49\u0026ndash;70) and presented with lower white blood cell (WBC) counts (mean 15.0 vs. 52.9 \u0026times;10\u0026sup3;/\u0026micro;L). Elevated WBC counts (\u0026gt;\u0026thinsp;100 \u0026times;10\u0026sup3;/\u0026micro;L) were most common among those treated within five days (19.1%). Adverse ELN risk was more frequent in the \u0026gt;\u0026thinsp;10-day group (46.7%) than in the \u0026lt;\u0026thinsp;1\u0026ndash;5-day group (38.3%, Fisher's exact test, p\u0026thinsp;=\u0026thinsp;0.005). High-intensity induction therapy was more often administered to patients with early DTI (77.5% for \u0026lt;\u0026thinsp;1\u0026ndash;5 days vs 57.2% for \u0026gt;\u0026thinsp;10 days; Fisher's exact test, p\u0026thinsp;\u0026lt;\u0026thinsp;0.001).\u003c/p\u003e\u003cp\u003eKaplan\u0026ndash;Meier survival curves demonstrated substantial overlap across DTI categories, with no significant difference by log-rank test (p\u0026thinsp;=\u0026thinsp;0.982; WBC\u0026thinsp;\u0026le;\u0026thinsp;100 \u0026times; 10\u0026sup3;/\u0026micro;L subgroup p\u0026thinsp;=\u0026thinsp;0.949) (Fig.\u0026nbsp;1). Similarly, unadjusted Cox analyses revealed no significant association between DTI and OS, with HRs near 1 for both the 6\u0026ndash;10 day and \u0026gt;\u0026thinsp;10-day groups relative to the \u0026lt;\u0026thinsp;1\u0026ndash;5 day reference.\u003c/p\u003e\u003cp\u003eAfter multivariable adjustment for age, WBC count, ELN risk, and treatment intensity (\u003cb\u003eTable\u0026nbsp;2\u003c/b\u003e), a prolonged DTI (\u0026gt;\u0026thinsp;10 days) was associated with improved survival, corresponding to a 32% reduction in mortality risk compared with early treatment (HR 0.68, 95% CI: 0.53\u0026ndash;0.87, p\u0026thinsp;=\u0026thinsp;0.003). Subgroup analyses (\u003cb\u003eTable\u0026nbsp;3\u003c/b\u003e) revelated that this benefit was most pronounced among older patients (\u0026gt;\u0026thinsp;65 years) with WBC\u0026thinsp;\u0026le;\u0026thinsp;100 \u0026times;10\u0026sup3;/\u0026micro;L, in whom a DTI\u0026thinsp;\u0026gt;\u0026thinsp;10 days conferred a 38% lower mortality risk compared with treatment within five days (HR 0.62, 95% CI: 0.39\u0026ndash;0.99, adjusted p\u0026thinsp;=\u0026thinsp;0.040). Within this same subgroup, outcomes were also superior for patients treated after \u0026gt;\u0026thinsp;10 days compared with those treated within 6\u0026ndash;10 days (HR 0.53, 95% CI: 0.30\u0026ndash;0.95, adjusted p\u0026thinsp;=\u0026thinsp;0.024). No significant survival differences by DTI were observed among younger patients (\u0026le;\u0026thinsp;65 years) or among those with WBC\u0026thinsp;\u0026gt;\u0026thinsp;100 \u0026times;10\u0026sup3;/\u0026micro;L after adjustment for covariates.\u003c/p\u003e\u003cp\u003eIndependent of DTI, several factors were significantly associated with survival. Adverse predictors included older age (per year; HR 1.03, 95% CI 1.02\u0026ndash;1.04), higher WBC count (per 10\u0026sup3;/\u0026micro;L; HR 1.002, 95% CI 1.001\u0026ndash;1.004), intermediate ELN risk (HR 1.70, 95% CI 1.22\u0026ndash;2.37), adverse ELN risk (HR 2.12, 95% CI 1.54\u0026ndash;2.94), and low-intensity therapy vs high-intensity (HR 1.64, 95% CI 1.27\u0026ndash;2.13) \u003cb\u003e(Table\u0026nbsp;2)\u003c/b\u003e. These associations were similar in interaction models, with older age (\u0026gt;\u0026thinsp;65 vs\u0026thinsp;\u0026le;\u0026thinsp;65) (HR 2.14, 95% CI 1.54\u0026ndash;2.98), intermediate ELN risk (HR 1.76, 95% CI 1.26\u0026ndash;2.46), adverse ELN risk (HR 2.20, 95% CI 1.59\u0026ndash;3.05), and low-intensity therapy (HR 1.81, 95% CI 1.41\u0026ndash;2.31) continuing to predict inferior outcomes \u003cb\u003e(Table\u0026nbsp;4)\u003c/b\u003e. The only factor independently associated with improved OS was a prolonged DTI\u0026thinsp;\u0026gt;\u0026thinsp;10 days, an effect restricted to older patients with lower WBC counts, as noted above.\u003c/p\u003e\u003cp\u003eThe proportional hazards assumption was assessed with Schoenfeld residuals. Although the global test approached significance (p\u0026thinsp;=\u0026thinsp;0.049), the assumption held for the DTI variable (p\u0026thinsp;=\u0026thinsp;0.332), corroborated by residual plots showing no systematic deviation (Fig.\u0026nbsp;2).\u003c/p\u003e"},{"header":"Discussion","content":"\u003cp\u003eOur findings reveal an unexpected association between the DTI and outcomes in older patients with AML. Specifically, prolonged DTI was associated with reduced mortality in older patients, whereas no survival benefit was observed in younger patients. Even among young patients with elevated WBC counts, treatment delay did not significantly influence outcomes. This observation differentiates our analysis from prior large registry studies, such as the German Study Alliance Leukemia\u0026ndash;Acute Myeloid Leukemia (SAL-AML) and TriNetX registry or reports by R\u0026ouml;llig et al. and Bertolli et al, which found no significant impact of DTI on survival.\u003csup\u003e\u003cspan citationid=\"CR11\" class=\"CitationRef\"\u003e11\u003c/span\u003e,\u003cspan citationid=\"CR12\" class=\"CitationRef\"\u003e12\u003c/span\u003e,\u003cspan citationid=\"CR13\" class=\"CitationRef\"\u003e13\u003c/span\u003e\u003c/sup\u003e\u003c/p\u003e\u003cp\u003eAnother large retrospective study of 1,317 patients from the Cleveland Clinic and the MD Anderson Cancer Center reported lower complete response (CR) and OS rates among young patients when DTI exceeded five days, while outcomes among older patients remained unaffected.\u003csup\u003e\u003cspan citationid=\"CR6\" class=\"CitationRef\"\u003e6\u003c/span\u003e\u003c/sup\u003e Similarly, an ECOG study of 362 patients demonstrated lower CR rates with delayed therapy initiation, although this did not translate into an OS difference.\u003csup\u003e\u003cspan citationid=\"CR13\" class=\"CitationRef\"\u003e13\u003c/span\u003e\u003c/sup\u003e\u003c/p\u003e\u003cp\u003eEvaluating the effect of DTI is inherently complex due to selection bias inherent to retrospective study designs. To mitigate this bias, we stratified patients by WBC count. Interestingly, even in patients with hyperleukocytosis, prolonged DTI did not adversely influence outcomes. Other potential confounders, such as disseminated intravascular coagulopathy (DIC), active infection/ or sepsis, and transfusion requirements, may also have contributed to differences in early mortality and treatment tolerance.\u003c/p\u003e\u003cp\u003eTo our knowledge, this is the first study to demonstrate a potential adverse impact of shorter DTI in older patients with AML. Several explanations may account for this finding. AML is a biologically and clinically heterogeneous disease, and older patients who received therapy earlier may have presented with greater clinical instability or more aggressive disease features, prompting expedited treatment initiation. Such patients may also have been less physiologically fit, predisposing them to treatment-related complications and early mortality. Our dataset did not capture clinical parameters such as infection or DIC, which limits our ability to test this hypothesis directly. Furthermore, our cohort largely predated the widespread use of venetoclax-based regimens, which may limit applicability to contemporary treatment paradigms.\u003csup\u003e\u003cspan citationid=\"CR14\" class=\"CitationRef\"\u003e14\u003c/span\u003e\u003c/sup\u003e\u003c/p\u003e\u003cp\u003eGiven these considerations, our results should be regarded as hypothesis-generating rather than definitive evidence of causality. Notably, prior studies examining DTI in AML have employed heterogeneous definitions of \u0026ldquo;delay\u0026rdquo;, with intervals varying widely across analyses. Some modeled DTI as a continuous variable, while others used categorical thresholds, as in our study. A prior meta-analysis suggested that median DTI across studies typically ranged from four to eight days.\u003csup\u003e\u003cspan citationid=\"CR15\" class=\"CitationRef\"\u003e15\u003c/span\u003e\u003c/sup\u003e\u003c/p\u003e\u003cp\u003eOur study has several limitations. First, its retrospective design introduces potential selection bias and confounding by indication, as patients perceived to be more acutely ill were likely prioritized for earlier treatment. Second, the landmark analysis, while essential to minimize immortal time bias, inherently excluded patients who died within 10 days of diagnosis, thereby limiting generalizability to early survivors. Third, data granularity was constrained: precise treatment initiation dates were unavailable, necessitating calculating of OS from the date of diagnosis rather than from the start of therapy. This approach, although standard, reflects the full disease trajectory rather than isolating post-treatment survival.\u003c/p\u003e\u003cp\u003e\u003cb\u003eConclusion\u003c/b\u003e In this multi-institutional retrospective study, a prolonged diagnosis-to-treatment interval was associated with improved survival among older patients with newly diagnosed AML, particularly those with lower white blood cell counts, while no adverse effect of treatment delay was observed in younger patients. These findings challenge the traditional assumption that immediate initiation of therapy universally improves outcomes and underscore the importance of individualized treatment timing in the era of precision oncology. Prospective studies are warranted to validate these results and to determine whether a brief delay to obtain comprehensive molecular data and optimize therapeutic selection may improve outcomes in clinically stable patients.\u003c/p\u003e"},{"header":"Declarations","content":"\u003cp\u003e\u003cstrong\u003eAcknowledgments:\u003c/strong\u003e The authors used an artificial intelligence-based tool for scholarly writing, specifically “Paperpal,” to assist with refining the English language and improving writing quality. No AI tools were used to summarize the content or any other form of writing. The authors take full responsibility for the content of this manuscript.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eThere was no funding associated with this paper.\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eConflict of Interest:\u0026nbsp;\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eFEC reports Consultant: SPD Oncology, Amgen, CTI BioPharma, AbbVie, MorphoSys, PharmaEssentia, BMS, Geron, Sobi, DAVA Oncology, Taiho Oncology, Daiichi Sankyo, Syndax, Novartis, Merck.\u003c/p\u003e\n\u003cp\u003eCL does consulting for AbbVie, Astellas, Arcellx, Syndax, Kura, Rigel, Stemline, Geron, Daiichi, and BMS, and has research funding from Jazz Pharma and BMS.\u003c/p\u003e\n\u003cp\u003eMEP has research funding to her institution from Abbvie, Ascentage, Astex, Oncoverity, and Pfizer\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAuthors contributions:\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eSN, FEC, IT, MEP and CL contributed to study conception and design.\u0026nbsp;Material preparation, data collection and analysis were performed by Samah Nassereddine, Vanyal Aggarwal, Kimberly Doucette, Lacy Williams, Leah Wells, Ramy Elsarrag, Jordan Selep, Yuan Feng, and\u0026nbsp;Shanshan Liu, Guoquing Diao.\u0026nbsp;The first draft of the manuscript was written by Samah Nassereddine and all authors commented on previous versions of the manuscript.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eEthics and Consent to Participate declarations: not applicable\u003c/strong\u003e\u003c/p\u003e"},{"header":"References","content":"\u003col\u003e\u003cli\u003e\u003cspan\u003eSekeres MA, Elson P, Kalaycio ME et al (2009) Time from diagnosis to treatment initiation predicts survival in younger, but not older, acute myeloid leukemia patients. 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J Clin Oncol 29(33):4417\u0026ndash;4423. \u003cspan class=\"ExternalRef\"\u003e\u003cspan class=\"RefSource\"\u003e10.1200/JCO.2011.35.7525\u003c/span\u003e\u003cspan address=\"10.1200/JCO.2011.35.7525\" targettype=\"DOI\" class=\"RefTarget\"\u003e\u003c/span\u003e\u003c/span\u003e\u003c/span\u003e\u003c/li\u003e\u003c/ol\u003e"},{"header":"Tables","content":"\n\u003cp\u003eTables 1 to 4 are available in the Supplementary Files section.\u003c/p\u003e\n"}],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":true,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":false,"hideJournal":false,"highlight":"","institution":"","isAcceptedByJournal":true,"isAuthorSuppliedPdf":false,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":false,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"[email protected]","identity":"annals-of-hematology","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":false,"externalIdentity":"aohe","sideBox":"Learn more about [Annals of Hematology](http://link.springer.com/journal/277)","snPcode":"277","submissionUrl":"https://submission.nature.com/new-submission/277/3","title":"Annals of Hematology","twitterHandle":"","acdcEnabled":true,"dfaEnabled":true,"editorialSystem":"stoa","reportingPortfolio":"Springer Hybrid","inReviewEnabled":true,"inReviewRevisionsEnabled":false},"keywords":"Acute myeloid leukemia, diagnosis-to-treatment interval, induction chemotherapy, molecular testing, risk stratification, targeted therapy, precision medicine, treatment outcomes","lastPublishedDoi":"10.21203/rs.3.rs-8147567/v1","lastPublishedDoiUrl":"https://doi.org/10.21203/rs.3.rs-8147567/v1","license":{"name":"CC BY 4.0","url":"https://creativecommons.org/licenses/by/4.0/"},"manuscriptAbstract":"\u003cp\u003e\u003cstrong\u003eBackground:\u003c/strong\u003eAcute myeloid leukemia (AML) is considered an oncologic emergency, yet the optimal timing for treatment initiation remains uncertain.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eMethods:\u003c/strong\u003e We conducted a multi-institutional retrospective study of 698 adults with newly diagnosed AML presenting to four academic centers across the United States. Diagnosis-to-treatment intervals (DTI) were categorized as \u0026lt;5 days, 5–10 days, and \u0026gt;10 days. Outcomes were analyzed using multivariable models adjusting for age, treatment intensity, ELN 2017 risk classification, and white blood cell count.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eResults:\u003c/strong\u003e Among younger patients, DTI was not associated with differences in survival outcomes. In contrast, older patients demonstrated improved survival with delayed treatment (DTI \u0026gt;10 days), particularly those with lower white blood cell counts. No adverse effects from treatment delay were observed in younger cohorts.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eConclusions:\u003c/strong\u003e This retrospective study has showed that prolonged DTI is associated with improved survival in older adults with newly diagnosed AML, challenging the traditional assumption that immediate therapy universally improves outcomes. These findings underscore the importance of individualized treatment timing in the era of precision oncology.\u003c/p\u003e","manuscriptTitle":"Impact of Diagnosis-to-Treatment Interval on the Outcome of Patients with Acute Myeloid Leukemia","msid":"","msnumber":"","nonDraftVersions":[{"code":1,"date":"2025-12-08 12:53:37","doi":"10.21203/rs.3.rs-8147567/v1","editorialEvents":[{"type":"communityComments","content":0},{"type":"decision","content":"Revision requested","date":"2026-01-24T11:16:01+00:00","index":"","fulltext":""},{"type":"editorInvitedReview","content":"","date":"2026-01-04T20:17:33+00:00","index":"hide","fulltext":""},{"type":"editorInvitedReview","content":"","date":"2026-01-02T02:53:29+00:00","index":"hide","fulltext":""},{"type":"reviewerAgreed","content":"264157259097166423984732890828249357470","date":"2025-12-09T20:50:21+00:00","index":"hide","fulltext":""},{"type":"reviewerAgreed","content":"114945701664186207100413344567867042310","date":"2025-12-06T21:54:39+00:00","index":"hide","fulltext":""},{"type":"reviewersInvited","content":"","date":"2025-12-04T20:46:18+00:00","index":"","fulltext":""},{"type":"editorAssigned","content":"","date":"2025-11-27T08:08:03+00:00","index":"","fulltext":""},{"type":"checksComplete","content":"","date":"2025-11-27T08:06:23+00:00","index":"","fulltext":""},{"type":"submitted","content":"Annals of Hematology","date":"2025-11-18T16:09:44+00:00","index":"","fulltext":""}],"status":"published","journal":{"display":true,"email":"[email protected]","identity":"annals-of-hematology","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":false,"externalIdentity":"aohe","sideBox":"Learn more about [Annals of Hematology](http://link.springer.com/journal/277)","snPcode":"277","submissionUrl":"https://submission.nature.com/new-submission/277/3","title":"Annals of Hematology","twitterHandle":"","acdcEnabled":true,"dfaEnabled":true,"editorialSystem":"stoa","reportingPortfolio":"Springer Hybrid","inReviewEnabled":true,"inReviewRevisionsEnabled":false}}],"origin":"","ownerIdentity":"1bfca859-8fdd-4968-80f4-142b55e8b581","owner":[],"postedDate":"December 8th, 2025","published":true,"recentEditorialEvents":[],"rejectedJournal":[],"revision":"","amendment":"","status":"under-review","subjectAreas":[],"tags":[],"updatedAt":"2026-05-01T05:56:08+00:00","versionOfRecord":[],"versionCreatedAt":"2025-12-08 12:53:37","video":"","vorDoi":"","vorDoiUrl":"","workflowStages":[]},"version":"v1","identity":"rs-8147567","journalConfig":"researchsquare"},"__N_SSP":true},"page":"/article/[identity]/[[...version]]","query":{"redirect":"/article/rs-8147567","identity":"rs-8147567","version":["v1"]},"buildId":"8U1c8b4HqxoKbykW_rLl7","isFallback":false,"isExperimentalCompile":false,"dynamicIds":[84888],"gssp":true,"scriptLoader":[]}