Intro
Adolescent and young adult cancer (AYAC) refers to new-onset cancers in people aged 15–39 years. 1 With the large increase in highly-specialized diagnostic and therapeutic approaches over past decades, the five-year survival rate of AYAC has surpassed 80%. 2 Nevertheless, the extended life-span does not necessarily indicate that patients have successfully adjusted to or coped with this condition; on the other hand, some common side effects resulting from treatment-related toxicity may have serious physical and psychological consequences on patients and their families. 3 Factually, the chronicity impact of AYAC in females has captured more attention than in males, involving breast cancer, thyroid cancer, melanoma, and cervical cancer. 4 Worse yet, the effects of cancer-related therapies on endocrine and reproductive organ function often persist long after diagnosis and treatment, thus exerting a heavy toll on females diagnosed with AYAC.
Presently, premature ovarian insufficiency (POI) has been noticed as a relevant disease due to cancer-related therapies toexacerbate ovarian function. 5 This is an imperative issue for females with AYAC since they may encounter disturbance in fertility later. POI is defined as the loss or decline of normal ovarian function before the age of 40, characterized by irregular or absent menstruation, hypoestrogenism, and elevated gonadotropin levels. 5 A population-based study revealed that AYAC survivors were nearly three times more likely to suffer from POI than the cancer -free counterparts. 6 Upon the onset of POI, the affected patients may face higher risks of cardiovascular disease, osteoporosis, cognitive dysfunction, and premature mortality later in life. 7–9 A commonly used approach to treat ovarian dysfunction in females undergoing cytotoxic chemotherapy so far is to prescribe gonadotropin-releasing hormone agonist (GnRHa). 10 Both the European Society of Human Reproduction and Embryology (ESHRE) and the American Society for Reproductive Medicine (ASRM) recommend prescribing GnRHa to mitigate the risk of ovarian insufficiency. 11 Despite the potential benefits of GnRHa, cancer females who received treatment-related gonadotoxicity still tend to sustain POI onset. 12 On top of that, mounting evidence shows that its use had deleterious impact on bone and cardiovascular health. 13 , 14 As a consequence, it is of great importance to broaden research and clinical horizons and explore potential adjunctive treatment methods against the onset of POI in AYAC females.
Known for having minor side effect, Chinese Herbal Medicine (CHM) has been extensively used for the therapeutic and prophylactic management of human disease, including POI. 15 , 16 Evidence suggests that CHM could exert its advantage on POI prevention through multiple signaling pathways, like caspase-mediated pathways and Nrf2 signaling pathway. 17 Plant-derived compounds have been further proven to possess immunomodulatory and anti-inflammatory actions that significantly inhibit release and function of inflammatory parameters, 18 which is known to severely affect ovarian function. 19 Accumulating evidence has documented the beneficial effects of CHM so far, but its impact on POI prevention in females withAYAC has yet to be confirmed. This study is, therefore, geared to clarify the association between CHM use and risk of chemotherapy-induced POI among AYAC females.
Methods
The target population for this nested patient-control study was obtained from a nationwide claims database in Taiwan that is maintained by the Bureau of National Health Insurance (NHI). 20 Through random sampling of all beneficiaries under the NHI program by age and sex, this database provides researchers an opportunity to undertake population-based studies and epidemiological investigations. The database includes encrypted beneficiary information on sex, birth date, and physician billing claims for inpatient and outpatient visits covered by the NHI, allowing for the identification of all medical consultations and diagnoses. Relevant medical diagnoses are coded using the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM). Since the data were anonymized before public release, individual identifying information cannot be obtained from the database. This study was conducted in accordance with the guidelines of the Helsinki Declaration. As all data were anonymized shown in this nationwide claims database, the Institutional Review Board of Buddhist Dalin Tzu Chi Hospital confirmed that this study was exempt from full review along with the need for informed consent in this study (No. B10004021-3).
The initial cohort included females with AYAC who were 20–39 years of age and had undergone chemotherapy for AYAC between 2002 and 2010 (ICD-9-CM code: 140–176, 185–208). To diminish misclassification bias, the lists of AYAC were further linked to the catastrophic illness card (CIR). This is because all citizens of Taiwan with autoimmune illnesses or malignancies can apply for the CIR certification to minimize the expenses of healthcare received. Prior to acquiring CIR, the experts employed in NHI would deliberately review the records of treatments received. These checks and processes are believed to ensure accurate coding to minimize ascertainment bias. Date of approval for the CIR card for AYAC was then regarded as the cohort entry date. To adhere to established research procedures, we excluded subjects who had been followed for less than one year and those with incomplete data (n = 504). Patients who underwent ovarian or uterine surgery also were deleted. Women for whose first AYAC diagnosis occurring after POI onset were removed to ensure the appropriate temporal sequence (n = 1115). The remaining patients were followed up until the earliest diagnosis of POI, death, or the end of 2013.
The primary outcome was the onsetof POI that occurred from 2003 to 2013. Participants were defined as having POI if they ever visited the outpatient clinic twice in one year or were hospitalized once during the study timeframe due to this condition (ICD-9-CM codes 627). 21 The first medical visit for POI was viewed as the index date. Each of the POI patients was randomly matched to one control with no POI diagnosis in accordance with age, socidemographic data and comorbidities ( Figure 1 ). An index date was assigned to each of the controls corresponding to the POI diagnosis date, which ensured the same observational frame for all enrollees.
Figure 1 Flowchart of subject selection.
Flowchart of subject selection.
The identification of CHM treatment is based on medical records indicating that visits to Chinese medicine practitioners that occurred from cohort entry date to the index date. In accordance with former method, 22 the participants were then converted into CHM users and non-CHM users based on if they ever received relevant CHM treatments for AYAC or its symptomsby intervals of 30 days, made by CHM physicians. Exposure to CHM use wasfurther split into two subgroups according to individual age at baseline. This subgroup analysis allowed us to appraise if the association between adjunctive CHM treatment and subsequent POI occurred across diverse age groups.
Covariates in the statistical model included sex, age, previous medical comorbidities, individual monthly salary, and urbanization level of residence. Health insurance premiums, used as a substitute for monthly salary, wereseparated into three quartile values, where level one stood for the lowest monthly salary group. As to the enrollees’ residential district, it was subdivided into three groups in accordance with the established method that took into account several factors, like population density per square kilometer, the proportion of individuals with a bachelor’s degree or higher, the ratio of residents aged 65 years or older, the percentage of the labor force employed in agriculture, and the number of clinicians per 100,000 inhabitants. 23 This indicator enables researchers to consider the enrollee’s healthcare accessibility. Medical comorbidities were defined as conditions that occurred at least once in inpatient, or twice in outpatient, claims one year prior to cohort entry. The Charlson–Deyo comorbidity index (CCI), a method that ranks the number and severity of 17 pre-defined comorbid conditions by assigning a weighted scale of 1 to 6, was adopted to categorize the baseline comorbidity burden for each patient. 24
Statistical analyses were conducted using SAS for Windows, Version 9.4. Descriptive statistics, including the mean, standard deviation (SD), frequency, and percentages, were used to assess the baseline patients’ characteristics. Baseline data were compared for treated and control groups using Student’s t -test test for continuous variables or chi-square test for categorical variables, as appropriate. Conditional logistic regression was used to estimate odds ratios (OR) with 95% confidence intervals (CI) for the relationship between CHM use and the subsequent incidence of POI. The adjusted OR (AOR) was also used to determine whether the adjustments shown in Table 1 would affect the results of CHM treatment. In all statistical tests, p ≤ 0.05 was considered significant. Table 1 Comparison of Demographic Data and Selected Comorbidities for AYAC Females with and without POI Number (%) POI Patients Non-POI Patients p N = 1040 (%) N = 1040 (%) Age (years) 0.62 ≤30 403 (19.4) 197 (18.9) 206 (19.8) >30 1677 (80.6) 843 (81.1) 834 (80.2) Mean (SD) 34.8 (5.1) 34.7 (5.2) 34.9 (4.9) 0.47 Monthly income 0.14 Level 1 1268 (61.0) 629 (60.5) 639 (61.4) Level 2 737 (35.4) 381 (36.6) 356 (34.3) Level 3 75 (3.6) 30 (2.9) 45 (4.3) Residential area 0.42 Urban 1363 (65.5) 678 (65.2) 685 (65.9) Suburban 306 (14.7) 163 (15.7) 143 (13.7) Rural 411 (19.8) 199 (19.1) 212 (20.4) CCI 1.7 (5.0) 1.9 (5.7) 1.5 (4.4) 0.12 Abbreviations : SD, standard deviation; CCI, Charlson–Deyo comorbidity index.
Comparison of Demographic Data and Selected Comorbidities for AYAC Females with and without POI
Abbreviations : SD, standard deviation; CCI, Charlson–Deyo comorbidity index.
Results
Among the recruited subjects, matching those with POI to those without POI resulted in 1040 cases in each group. Descriptive statistics showed no remarkable differences in demographic or clinical features between patients with and with no POI after random matching procedure ( Table 1 ). The mean age for enrollees was 34.8 years (SD= 5.1 years). Over 60% of participants resided in an urban area and had a low-level income.
Within the study period, 17.6% of POI patients and 56.1% of non-POI patients received adjunctive CHM treatment after AYAC. Multivariate conditional logistic regression analysis showed that those with a history of CHM use were 84% less likely to have POI than those not receiving CHM treatment. The positive effect of CHM treatment on the prevention of POI risk was predominant among patients ≤ 30 years of age ( Table 2 ). CHM use provided the greatest therapeutic benefit when it was initiated within the first 3 years after AYAC onset (AOR, 0.08; 95% CI, 0.03–0.17). The association between CHM use and absence of POI gradually decreased with the delay of CHM initiation ( Table 3 ). Table 2 Association Between POI Onset and CHM Use by Age Group CHM Use POI Patients (n = 1040) Non-POI Patients (n =1040) OR (95% CI) AOR* (95% CI) Non-CHM users 857 82.4 457 43.9 1 1 CHM users 183 17.6 583 56.1 0.17 (0.14–0.19) 0.16 (0.13–0.19) Age ≤ 30 150 14.4 293 28.2 0.05 (0.03–0.10) 0.05 (0.03–0.10) Age >30 33 3.2 290 27.9 0.20 (0.16–0.25) 0.20 (0.16–0.24) Note : *Adjusted for potential confounders including age, residential area, monthly income, and CCI scores. Abbreviations : CHM, Chinese herbal medicines; OR, odds ratio; CI, confidence interval.
Table 3 Risk of POI in AYAC Females with and without Receiving CHM Stratified by Time of CHM Commencement Years After AYAC Onset Non-CHM Users CHM Users OR 95% CI AOR * 95% CI 6 years 1 Reference 1.01 0.46–1.84 Note : *Model adjusted for age, urbanization level, monthly income, and comorbidities.
Association Between POI Onset and CHM Use by Age Group
Note : *Adjusted for potential confounders including age, residential area, monthly income, and CCI scores.
Abbreviations : CHM, Chinese herbal medicines; OR, odds ratio; CI, confidence interval.
Risk of POI in AYAC Females with and without Receiving CHM Stratified by Time of CHM Commencement
Note : *Model adjusted for age, urbanization level, monthly income, and comorbidities.
Table 4 displayed the top ten most commonly prescribed single-herb and multi-herb formulae for the treatment of AYAC (). From them, we identifiedseveral potential agents that were correlated with a lower risk of POI, which included Da-Huang, Xiang-Fu, Ping-Wei-San, Ge-Gen-Tang, Xin-Yi-Qing-Fei-Tang, Jia-Wei-Xaio-Yao-San, and Shao-Yao-Gan-Cao-Tang ( Figure 2 ). Table 4 The Ingredient Herbs Contained in the Most-Used Single-Herb and Multi-Herb Products Among Participants Chinese Herbal Product Ingredients Number of Prescriptions Functional Classification Single-herb products Da-Huang Radix et Rhizoma Rhei; Rheumpalmatum L. 1790 Purgatives Bai-Zhi Radix Angelicae Dahuricae; Angelicadahurica (Fisch. ex Hoffm.) Benth. et Hook. f. var. formosana (Boiss.) Shan et Yuan 1229 Expelling expression, dispelling wind, dispelling dampness Yan-Hu-Suo Corydalis Rhizoma; Corydalisyanhusuo (Y. H. Chou & Chun C. Hsu) W. T. Wang ex Z. Y. Su & C. Y. Wu 1219 Relieves pain Anti-oxidative, anti-fibrotic, and anti-thrombotic effects. Xiang-Fu RhizomaCyperi; Cyperus rotundus L 1093 Unblocks Stagnant Liver Qi and relieves pain Bei-Mu Bulbus Fritillariae; Fritillaria thunbergii Miq. 1049 Transform phlegm HaiPiaoXiao Sepiae Endoconcha; Sepiellamaindroni de Rochebrune 929 Astringents Yi-Mu-Cao Herba Leonuri; Leonurus japonicus Houtt. 844 Improves blood circulation and reduces inflammation Tian-Hua-Fen Radix Trichosanthis; Trichosantheskirilowii Maxim. 786 Clear heat Ye-Jiao-Teng Caulis Polygoni Multiflori; Reynoutria multiflora (Thunb.) Moldenke 750 Nourishes the heart and calms the mind Shi-Gao Gypsum Fibrosum; CaSO4·2H2O 471 Clear heat and purge fire Multi-herb products Jia-Wei-Xiao-Yao-San Dang-Gui (Radix Angelicae Sinensis; Angelica sinensis (Oliv.) Diels), Bai-Shao (Radix Paeoniae Alba; Paeonia lactiflora Pall.), Fu-Ling (Poria; Wolfiporia cocos (Schw.) Ryv. and Cilbn.), Bai-Zhu (Rhizoma Atractylodis Macrocephalae; Atractylodesmacrocephala Koidz.), Chai-Hu (Radix Bupleuri; Bupleurum chinense DC.), Mu-Dan-Pi (Cortex Moutan; Paeonia × suffruticosa Andrews), Zhi-Zi (Fructus Gardeniae; Gardenia jasminoides J. Ellis), Gan-Cao (Radix Glycyrrhizae; Glycyrrhiza uralensis Fisch.), Bo-He (Herba Menthae Haplocalycis; Mentha alaica Boriss.), Sheng-Jiang (Rhizoma Zingiberis Recens; Zingiber officinale Roscoe) 3014 Pacifies the liver and strengthens the spleen Chuan-Xiong-Cha-Tiao-San Chuan-Xiong Bai-Zhi (Radix Angelicae Dahuricae; Angelica dahurica (Hoffm.) Benth. and Hook. f. ex Franch. and Sav.) Gan Cao (Radix Glycyrrhizae; Glycyrrhiza uralensis Fisch.) Qiang-Huo (Rhizoma et Radix Notopterygii; Notopterygiumincisum K. C. Ting ex H. T. Chang) Jing-Jie (Schizonepeta annua (Pall.) Schischk.) Xi–Xin (Herba cum Radix Asari; Asarum sieboldiiMiq.) Fang-Feng (Radix Saposhnikoviae; Saposhnikoviadivaricata (Turcz.) Schischk.) Bo-He (Herba Menthae Haplocalycis; Mentha alaica Boriss.) 1685 Dispersal of wind disorders Ge-Gen-Tang Ge-Gen (Radix Puerariae; Pueraria lobata (Willd.) Ohwi), Ma-Huang (Herba Ephedrae; Ephedra sinica Stapf), Gui-Zhi (Ramulus Cinnamomi; Cinnamomum cassia (L.) J. Presl), Bai-Shao (Radix Paeoniae Alba; Paeonia lactiflora Pall.), Sheng-Jiang (Rhizoma Zingiberis Recens; Zingiber officinale Roscoe), Da-Zao (Fructus Jujubae; Ziziphus jujuba Mill.), Gan Cao (Radix Glycyrrhizae; Glycyrrhiza uralensis Fisch.) 1357 Releases wind-cold in the exterior and muscle layer Ma Zi Ren Wan Huo-Ma-Ren (Semen Cannabis; Cannabis sativa L.); Xing-Ren (Semen Armeniacae Amarum; Prunus armeniaca L.); Bai-Shao (Radix Paeoniae Alba; Paeonia lactiflora Pall); Zhi-Shi (Fructus AurantiiImmaturus; Citrus aurantium L.); Hou-Po (Cortex Magnoliae; Magnolia officinalis); Da-Huang (Radix et Rhizoma Rhei; Rheum palmatum L.) 1256 lubricating and moistening the intestines and the stool Yin Qiao San Jin Yin Hua (Flos Lonicerae; Lonicera japonica Thunb.); Lian Qiao (Fructus Forsythiae; Forsythia suspensa (Thunb.) Vahl); Jie Geng (Radix Platycodi; Platycodongrandiflorus (Jacq.) A. DC); Niu Bang Zi (Fructus Arctii; Arctium lappa L.); Bo He (Herba Menthae; Mentha haplocalyx Briq); Gan Cao (Radix Glycyrrhizae; Glycyrrhiza uralensis) Fisch.); Dan Dou Chi (Semen Sojae Preparata; Glycine max (L.) Merr.); Dan Zhu Ye (Herba Lophatheri; Lophatherum gracile Brongn.); Jing Jie (Herba Schizonepetae; Schizonepeta tenuifolia); Lu Gen (Rhizoma Phragmitis; Phragmites communis Trin.) 1149 Dispels wind-heat, clears heat and detoxifies Shao-Yao-Gan-Cao-Tang Bai-Shao (Radix Paeoniae Alba; Paeonia lactiflora Pall.), Gan-Cao (Radix Glycyrrhizae; Glycyrrhiza uralensis Fisch.) 943 Nourishes Yin and relief painful spasms Ping-Wei-San Cang-Zhu (Rhizoma Atractylodis; Atractylodeslancea (Thunb.) DC.), Hou-Po (Cortex Magnoliae Officinalis; Magnolia officinalis Rehder & E. H. Wilson), Chen-Pi (Pericarpium Citri Reticulatae; Citrus reticulata Blanco), Gan-Cao (Radix Glycyrrhizae; Glycyrrhiza uralensis Fisch.), Sheng-Jiang (Rhizoma Zingiberis Recens; Zingiber officinale Roscoe), Da-Zao (Fructus Jujubae; Ziziphus jujuba Mill.) 901 Dries dampness and harmonizes the stomach Ban-Xia-Xie-Xin-Tang Ban Xia (Rhizoma Pinelliae; Pinelliaternata (Thunb.) Breit.), Huang Lian (Rhizoma Coptidis; Coptis chinensis Franch.), Huang Qin (Radix Scutellariae; Scutellariabaicalensis Georgi), Gan Jiang (Rhizoma Zingiberis; Zingiber officinale), Ren Shen (Radix Ginseng; Panax ginseng C. A. Mey.), Da Zao (Fructus Jujubae; Ziziphus jujuba Mill.), and Zhi Gan Cao (Radix Glycyrrhizae; Glycyrrhiza uralensis Fisch.) 864 Harmonizing cold and heat in the stomach and intestine Xin-Yi-Qing-Fei-Tang Xin-Yi (Flos Magnoliae; Magnolia biondii Pamp.), Pi-Pa-Ye (Fol. Eriobotryae; Eriobotrya japonica (Thunb.) Lindl.), Zhi-Zi (Fructus Gardeniae; Gardenia jasminoides J. Ellis), Zhi-Mu (Rhizoma Anemarrhenae; Anemarrhenaasphodeloides Bunge), Bai-He (Bulbus Lilii; Lilium brownii F. E. Br. ex Miellez), Huang-Qin (Radix Scutellariae; Scutellariabaicalensis Georgi), Sheng-Ma (Rhizoma Cimicifugae; Cimicifuga foetida L.), Mai-Men-Dong (Radix Ophiopogonis; Ophiopogon japonicus (Thunb.) Ker Gawl.), Shi-gao (Gypsum Fibrosum), Gan-cao (Radix Glycyrrhizae; Glycyrrhiza uralensis Fisch.) 804 Dispels lung heat and unblocks the nostril Gan-Lu-Yin Di-Huang (Radix Rehmanniae; Rehmanniaglutinosa (Gaertn.) DC.), Shi-Hu (Herba Dendrobii; Dendrobium loddigesii Rolfe), Tian-Men-Dong (Radix Asparagi; Asparagus cochinchinensis (Lour.) Merr.), Mai-Men-Dong (Radix Ophiopogonis; Ophiopogon japonicus (Thunb.) Ker Gawl.), Huang-Qin (Radix Scutellariae; Scutellariabaicalensis Georgi), Yin-Chen-Hao (Herba Artemisiae Scopariae; Artemisia capillaris Thunb.), Zhi-Ke (Fructus Aurantii; Citrus × aurantium L.), Pi-Pa-Ye (Folium Eriobotryae; Eriobotrya japonica (Thunb.) Lindl.), Gan-Cao (Radix Glycyrrhizae; Glycyrrhiza uralensis Fisch.) 749 Generates fluids and clears heat
Figure 2 Risk of POI in females with AYAC as determined by multivariate conditional logistic regression analysis.
The Ingredient Herbs Contained in the Most-Used Single-Herb and Multi-Herb Products Among Participants
Risk of POI in females with AYAC as determined by multivariate conditional logistic regression analysis.
Discussion
To the best of our knowledge, this study is the first to utilize the electronic health records to delineate the association between adjunctive CHM use and subsequent risk of POI among AYAC females undergoing chemotherapy-related treatments. We observed that CHM use correlated with a lower risk of POI. Furthermore, CHM users under the age of 30 experienced a significantly lower incidence of POI by over 90%, suggesting that the benefit of CHM for POI treatment is more pronounced in younger individuals. Importantly, the commencement of CHM treatment within three years after AYAC onset correlated with a notably lower risk of POI. The association between CHM use and lower POI risk reported herein were in accord with published data and extend our understanding of these medical conditions. 15–17 Several explanations underlay the protective effects of CHM for the prevention of POI, which may include modulation of apoptosis, immune response regulation, enhancement of antioxidant capacity, and estrogen-like activity. 16
One major breakthrough yielded by the findings of this study is the identification of specific CHM herbs that may act to prevent POI in females with AYAC. Several are single herbs, such as Da-Huang and Xiang-Fu, while others are multi-herb formulae that include Ge-Gen-Tang, Xin-Yi-Qing-Fei-Tang, Jia-Wei-Xaio-Yao-San, and Shao-Yao-Gan-Cao-Tang. We observed that Da-Huang use significantly decreased risk of POI. In clinical practice, Da-Huang has long been used for its diverse pharmacological properties, especially its ability to regulate ovarian function and influence fertility. Li et al found that aloe-emodin, one of the main pharmacodynamic ingredients of Da-Huang, inhibited growth and induced apoptosis of squamous cell carcinoma by regulating caspase-9 and caspase-3 levels. 25 In addition, Da-Huang has been shown to improve reproductive health by contributing to estrogen balance and supporting ovarian function. 26
We also observed that Xiang-Fu use was associated with a reduced risk of POI. The biological mechanism by which this herb could decrease the risk of POI may be related to its striking effect on hormone regulation. One recent in-vitro study demonstrated that Cyperus rotundos (Xiang-Fu) inhibits the mRNA expression of NF-kB through the Akt pathway. 27 The PI3K/Akt pathway is well known to regulate a variety of cellular events, including cell proliferation, apoptosis, immune response, and the oxidative stress response by regulating various intra- and extra-cellular signaling molecules. 28 This phenomenon may underlie the effects of this medication in females with AYAC.
This study shows that females with AYAC who took Ge-Gen-Tang were at lower chance of having POI. Pueraria, the primary component of Ge-Gen-Tang, is renowned for its reduced age-related vascular stiffening and improves endothelial-dependent vasodilation, Several scholars found that pueraria isoflavones, active compounds in Gegan, can balance estrogen levels, neutralize free radicals, and improve immune function. 29 A recent review article further elucidated that by modulating T-lymphocyte activity, reducing B-lymphocyte proliferation, and diminishing associated autoantibodies, the pueraria isoflavones can efficiently alleviate menopausal symptoms and improve ovarian function in POI patients. 16 Similarly, a positive correlation was observed between Xin-Yi-Qing-Fei-Tang use and a decreased risk of POI. Magnolin (Xin-Yi), a major constituent of Xin-Yi-Qing-Fei-Tang, has been traditionally prescribed for anti-inflammatory conditions. 30 By targeting ERK1/2 activity, Lee and coworkers observed that magnolin greatly suppressed RSK2 phosphorylation and downstream proteins, including ATF1, c-Jun, and AP-1, thus abating neoplastic cell transformation and its relevant late effects. 30 These underlying mechanisms may, therefore, account for the advantages of Ge-Gen-Tang and Xin-Yi-Qing-Fei-Tang reported in the current study.
Our results also show that uses of both Jia-Wei-Xaio-Yao-San and Shao-Yao-Gan-Cao-Tang positively correlated with a lower risk of POI. Jia-Wei-Xaio-Yao-San is the most frequently used CHM decoction for co-treatment with Tamoxifen in breast cancer patients undergoing hormone therapy. 31 Using a breast-cancer mouse model, a previous study found that this herb inhibited tumor growth in 4T1-tumor–induced mice via regulation of the Bcl-2/Bax/TP53 signaling pathway. 32 Jia-Wei-Xaio-Yao-San was found to exhibit dose-dependent antioxidative effects by inhibiting xanthine oxidase, an enzyme that converts xanthine to uric acid while producing superoxide anions as a byproduct. 33 Excessive immune and inflammatory responses in ovaries are well known to impair ovarian function by disrupting T cell subsets and stimulating B cells to produce anti-oocyte and anti-ovarian antibodies. 19 As to Shao-Yao-Gan-Cao-Tang, this herb has been traditionally used in the treatment of various gynecological disorders, including dysmenorrhea, polycystic ovary syndrome, endometriosis, and adenomyosis. Recent studies have shown that this formula exerts dose-dependent reductions in body weight and chronic inflammation by inhibiting the Toll-like receptor 4 /NF-κB signaling pathway. 34 , 35 Suppression of this inflammation-linked pathway has been shown to eliminate endogenous peroxidases and inflammation, thus likely decreasing the risk of POI.
Despite the important public health implications of this study, it has several limitations and raises questions that are not fully resolved by this study. First, the claims-based database that we used lacks some pertinent information, such as physical activity, psychosocial variables, dietary intake and biomedical data. Future studies should further aim to overcome these drawbacks to validate the accuracy of our findings, especially indiverse AYAC types. Nonetheless, given the magnitude and statistical significance of the observed effect in this large-scale survey, these limitations are unlikely to affect our findings. Second, the use of secondary healthcare databases may have resulted in the accidental inclusion of miscoded patients, thereby introducing misclassification bias. To minimize this drawback, we only included individuals with new-onset AYAC or POI, and only after they had at least two outpatient visits reporting consistent diagnoses or at least one inpatient admission. It should also be acknowledged that the NHI of Taiwan randomly reviews charts and audits medical charges to assure the authenticity of claims files. Furthermore, since the coding approach and data availability were similar for the two groups, any misclassification bias would likely have been nondifferential, thus biased towards demonstrating no relationships between CHM use and POI risk. Third, despite the substantial correlation between CHM use and the subsequent lower risk of POI in females with AYAC, caution must be exerted in interpreting the results since participants were not randomly categorized into treated and control groups at the beginning of the study. For the sake of these reasons, the well-controlled, randomized, prospective, multicenter large clinical explorations are required to further validate the evidence shown herein. Not only is this manner imperative for elucidating the potential mechanism of action of CHM herbs, it also makes interpretation of the findings more straightforward and clinically robust.
Conclusions
Given the serious consequences of POI in females with AYAC, improvements in available therapeutic modalities to minimize this condition are needed. Findings of the present study shed light on the beneficial addition of CHM treatment to standard cancer therapies, by demonstrating its association with a reduced risk of chemotherapy-induced POI, particularly for AYAC patients under the age of 30. Early initiation of CHM, especially within three years of AYAC onset, further decreased POI risk, indicating its potential benefit in the prevention of chemotherapy-induced gonadotoxicity. In addition to providing preliminary evidence of the beneficial effects of CHM in arresting the development of POI, this study paves the way for further in vivo studies of specific herbal prescriptions to explore their potential for treating POI. In clinical practice, healthcare practitioners should initiate monitoring of patients’ ovarian function on a regular basis. Last but not least, it is very important for health care professionals to recognize that aspects of cancer survivorship continue to require attention and possible follow-up care via the interdisciplinary caring strategies.
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