Evidence map›Paper›PMID 42860940›Full record

ArticleGynecology and pelvic medicine2026

Survival trends and prognostic factors of metastatic cervical cancer: a population-based cohort study.

Cheng Wang, Cai Xu, Xingchen He, Wei Wang, Rutie Yin, Jing Zeng

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Article in Gynecology and pelvic medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Cheng WangDepartment of Pathology, West China Second University Hospital of Sichuan University, Chengdu, China.
Cai XuDepartment of Radiation Oncology, University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Xingchen HeDepartment of Endocrinology and Metabolism, MAGIC China Center, West China Hospital of Sichuan University, Chengdu, China.
Wei WangDepartment of Pathology, West China Second University Hospital of Sichuan University, Chengdu, China.
Rutie YinKey Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, China.
Jing ZengKey Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, China.ORCID https://orcid.org/0009-0002-9636-6324

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Metastatic cervical cancer (mCC) remains a highly lethal disease. While clinical trials support the addition of targeted therapy and immunotherapy to chemotherapy, real-world survival trends are less well characterized. This study aimed to evaluate real-world overall survival trends and prognostic factors in mCC patients over the past two decades, in the context of evolving targeted and immunotherapeutic treatments. Methods: We conducted a retrospective cohort study using the Surveillance, Epidemiology, and End Results (SEER) database to evaluate overall survival (OS) trends and prognostic factors among mCC patients diagnosed between 1998 and 2019. Based on major therapeutic milestones, patients were grouped into three calendar cohorts: 1998-2003 (pre-bevacizumab chemotherapy era), 2004-2013 (chemotherapy plus molecular-targeted therapy era), and 2014-2019 (chemotherapy plus immuno-molecular targeted therapy era, after pembrolizumab approval). Kaplan-Meier and Cox regression analyses were used to assess OS and identify independent prognostic variables. Results: Among 1,866 patients with distant mCC [corresponding to International Federation of Gynecology and Obstetrics (FIGO) stage IVB], 53.5% were aged ≥55 years and 67.1% had squamous cell carcinoma (SCC). Median OS increased from 11 months in 1998-2003 to 14 months in 2014-2019 (P=0.04), while the mortality rate declined from 91.6% in 1998-2003 to 75.9% in 2014-2019 (P<0.001). Among patients with SCC, median OS increased from 13 months in 1998-2003 to 16 months in 2014-2019 (P=0.006), whereas no significant survival improvement was observed among those with non-SCC histologies (P=0.48). Multivariable analysis identified SCC histology [hazard ratio (HR) =0.764, 95% confidence interval (CI): 0.670-0.871], lymphadenectomy (HR =0.730, 95% CI: 0.602-0.886), radiotherapy (HR =0.696, 95% CI: 0.619-0.783), and chemotherapy (HR =0.508, 95% CI: 0.452-0.571) were independently associated with improved survival. While age ≥55 years (HR =1.158, 95% CI: 1.045-1.284), Black race (HR =1.339, 95% CI: 1.108-1.620), absence of surgery (HR =2.160, 95% CI: 1.788-2.610), and local surgery alone (HR =1.501, 95% CI: 1.129-1.995) were associated with worse outcomes. Conclusions: Survival for mCC has improved in the past two decades, possibly because of the advances of local therapy and systemic therapy. However, outcomes remain poor for patients with non-SCC histologies, older patients, and Black patients, highlighting the need for individualized, multimodal treatment approaches and better access to emerging therapies.

Indexed as

Metastatic cervical cancer (mCC)prognostic factorsSurveillance, Epidemiology, and End Results (SEER)survival trendssystemic therapy

Identifiers

PMID42860940
PMCPMC13653788

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