Association between pelvic inflammatory disease and risk of ovarian, uterine, cervical, and vaginal cancers—a meta-analysis

In: Archives of Gynecology and Obstetrics · 2024 · vol. 310(5) , pp. 2577–2585 · doi:10.1007/s00404-024-07748-z · PMID:39327298 · W4402889635
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This meta-analysis of 13 observational studies found a significantly increased risk of ovarian, uterine, and vaginal cancers associated with a history of pelvic inflammatory disease.

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This meta-analysis evaluated whether a history of pelvic inflammatory disease (PID) is associated with increased risk of genitourinary cancers, synthesizing evidence from 13 observational studies published between 2016 and 2024 using pooled odds ratios and adjusted hazard ratios with heterogeneity assessed by I2. Across included comparisons, people with prior PID had higher odds of ovarian cancer (OR 1.477, 95% CI 1.033–2.207) and vaginal cancer (OR 2.500, 95% CI 1.400–4.000), while the uterine cancer estimate was not statistically significant (OR 1.263, 95% CI 0.827–2.143) and the cervical cancer estimate was near null (OR 1.000, 95% CI 0.900–1.100). The authors noted high overall heterogeneity (I2 = 82.92%), indicating differing trends across populations and study designs as a key limitation. Relevance to endometriosis: endometriosis is not the paper’s focus, but the corpus relevance is supported because the reference list includes studies examining PID and endometriosis risk (e.g., “Association between pelvic inflammatory disease and risk of endometriosis”).

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Abstract

Background and aimThe present meta-analysis aims to investigate a potential link between pelvic inflammatory disease (PID) and an increased risk of genitourinary cancers (ovarian, cervical, uterus, and vagina cancers). While previous research has hinted at a possible link, this meta-analysis seeks to delve deeper into the available evidence. Understanding this association is crucial for preventive strategies and improving clinical management practices.MethodologyA comprehensive literature search was conducted across various databases, covering studies published between 2016 and 2024. We included 13 observational studies meeting stringent criteria, followed by meticulous data extraction and quality assessment. Meta-analytical techniques were then employed to calculate pooled odds ratios (ORs), adjusted hazard ratios (HRs), and 95% confidence intervals (CIs), with heterogeneity assessed using the I2 statistic.ResultsOur analysis revealed significant findings, underscoring the association between PID and increased risks of genitourinary cancers. Specifically, individuals with a history of PID demonstrated notably higher odds of developing ovarian cancer (OR = 1.477, 95% CI 1.033-2.207), uterine cancer (OR = 1.263, 95% CI 0.827-2.143), cervical cancer (OR = 1.000, 95% CI 0.900-1.100), and vaginal cancer (OR = 2.500, 95% CI 1.400-4.000) compared to those without such a history. The overall heterogeneity across studies was high (I2 = 82.92%), suggesting varying trends across different populations and study designs.ConclusionThis meta-analysis provides updated evidence supporting a significant association between PID and an increased risk of cervical, ovarian, and uterine cancers. Early detection and management of PID are crucial in potentially mitigating the risk of these cancers.
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Abstract

Background and aim The present meta-analysis aims to investigate a potential link between pelvic inflammatory disease (PID) and an increased risk of genitourinary cancers (ovarian, cervical, uterus, and vagina cancers). While previous research has hinted at a possible link, this meta-analysis seeks to delve deeper into the available evidence. Understanding this association is crucial for preventive strategies and improving clinical management practices. Methodology A comprehensive literature search was conducted across various databases, covering studies published between 2016 and 2024. We included 13 observational studies meeting stringent criteria, followed by meticulous data extraction and quality assessment. Meta-analytical techniques were then employed to calculate pooled odds ratios (ORs), adjusted hazard ratios (HRs), and 95% confidence intervals (CIs), with heterogeneity assessed using the I2 statistic.

Results

Our analysis revealed significant findings, underscoring the association between PID and increased risks of genitourinary cancers. Specifically, individuals with a history of PID demonstrated notably higher odds of developing ovarian cancer (OR = 1.477, 95% CI 1.033–2.207), uterine cancer (OR = 1.263, 95% CI 0.827–2.143), cervical cancer (OR = 1.000, 95% CI 0.900–1.100), and vaginal cancer (OR = 2.500, 95% CI 1.400–4.000) compared to those without such a history. The overall heterogeneity across studies was high (I2 = 82.92%), suggesting varying trends across different populations and study designs.

Conclusion

This meta-analysis provides updated evidence supporting a significant association between PID and an increased risk of cervical, ovarian, and uterine cancers. Early detection and management of PID are crucial in potentially mitigating the risk of these cancers. Similar content being viewed by others Data availability All the data supporting the findings of this study have been provided within the manuscript.

References

Chang CY-Y et al (2021) Association of pelvic inflammatory disease (PID) with ovarian cancer: a nationwide population-based retrospective cohort study from Taiwan. BMC Womens Health 21(1):1–7 Falconer H et al (2021) Association between pelvic inflammatory disease and subsequent salpingectomy on the risk for ovarian cancer. Eur J Cancer 145:38–43 Firat A (2022) Cumulative inflammatory burden causing multiple complications after a successful pelvic surgery for advanced ovarian cancer. Niger J Clin Pract 25(10):1762–1765 Greydanus DE, Cabral MD, Patel DR (2022) Pelvic inflammatory disease in the adolescent and young adult: an update. Dis Mon 68(3):101287 Haddad A et al (2020) Inflammatory bowel disease and prostate cancer risk: a systematic review. Arab J Urol 18(4):207–212 Hosseininasab-Nodoushan SA et al (2022) Association of chlamydia and mycoplasma infections with susceptibility to ovarian cancer: a systematic review and meta-analysis. Seminars Cancer Biol 86:923–928 Nebbia M, Yassin NA, Spinelli A (2020) Colorectal cancer in inflammatory bowel disease. Clin Colon Rectal Surg 33(05):305–317 Stewart L et al (2020) Association between pelvic inflammatory disease, infertility, ectopic pregnancy and the development of ovarian serous borderline tumor, mucinous borderline tumor and low-grade serous carcinoma. Gynecol Oncol 156(3):611–615 Sultana A et al (2022) Computational intelligence in healthcare applications. Elsevier, pp 101–120 Xu M et al (2021) Systemic inflammatory score predicts overall survival in patients with cervical cancer. J Cancer 12(12):3671 Ye H et al (2024) Association between pelvic inflammatory disease and risk of endometriosis: a systematic review and meta-analysis. J Womens Health 33(1):73–79 Jonsson S et al (2024) Pelvic inflammatory disease and risk of epithelial ovarian cancer: a national population-based case-control study in Sweden. Am J Obstet Gynecol 230(1):75.e15-75.e15 Huang JY, Ma KS, Wang LT, Chiang CH, Yang SF, Wang CH, Wang PH (2023) The risk of endometrial cancer and uterine sarcoma following endometriosis or pelvic inflammatory disease. Cancers (Basel) 15(3):833. https://doi.org/10.3390/cancers15030833 Tai F-W et al (2018) Association of pelvic inflammatory disease with risk of endometriosis: a nationwide cohort study involving 141,460 individuals. J Clin Med 7(11):379 Shen CC, Hu LY, Yang AC, Chiang YY, Hung JH, Tsai SJ (2016) Risk of uterine, ovarian and breast cancer following pelvic inflammatory disease: a nationwide population-based retrospective cohort study. BMC Cancer 16(1):839. https://doi.org/10.1186/s12885-016-2857-1 Park HK et al (2018) Benign gynecologic conditions are associated with ovarian cancer risk in African-American women: a case–control study. Cancer Causes Control 29:1081–1091 Fortner RT et al (2019) Sexually transmitted infections and risk of epithelial ovarian cancer: results from the nurses’ health studies. Br J Cancer 120(8):855–860 Stewart LM et al (2018) Risk of high-grade serous ovarian cancer associated with pelvic inflammatory disease, parity and breast cancer. Cancer Epidemiol 55:110–116 Rasmussen CB et al (2017) Pelvic inflammatory disease and the risk of ovarian cancer and borderline ovarian tumors: a pooled analysis of 13 case-control studies. Am J Epidemiol 185(1):8–20 Huang J-Y et al (2021) Different influences of endometriosis and pelvic inflammatory disease on the occurrence of ovarian cancer. Int J Environ Res Public Health 18(16):8754 Søgaard KK et al (2020) Pelvic inflammatory disease and risk of cancer: a nationwide cohort study. Int J Gynecol Obstet 149(1):107–109

Acknowledgements

This research has been funded by Scientific Research Deanship at University of Ha’il-Saudi Arabia through project number RG-21 049. Funding This research has been funded by Scientific Research Deanship at University of Ha’il-Saudi Arabia through project number RG-21 049. Author information Authors and Affiliations Corresponding author Ethics declarations Conflict of interest The authors declares that there is no conflict of interest regarding the publication of this paper. Additional information Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Rights and permissions Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. About this article Cite this article Syed Khaja, A., Saleem, M., Zafar, M. et al. Association between pelvic inflammatory disease and risk of ovarian, uterine, cervical, and vaginal cancers—a meta-analysis. Arch Gynecol Obstet 310, 2577–2585 (2024). https://doi.org/10.1007/s00404-024-07748-z Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s00404-024-07748-z

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