Evidence map›Paper›PMID 42574435›Full record

Observational studyPloS one2026

Efficacy comparison of concurrent chemoradiotherapy alone versus concurrent chemoradiotherapy plus adjuvant chemotherapy in stage III Locally Advanced Cervical Cancer: A single-center, retrospective observational cohort study.

Haizhou Yang, Yaxian Tan, Yajun Pang, Xiaowen Chen, Guoqiang Chen, Caixia Liang, Manyu Chen, Qiulong Liu, Zhihao Li, Jierong Xie and 3 more

Abstract readObservational StudyComparative Study
In one paragraph

Observational study in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Sequential chemoradiotherapyTranslational cancer research · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Haizhou YangDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.ORCID https://orcid.org/0000-0002-4105-9995
Yaxian TanDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Yajun PangDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Xiaowen ChenDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Guoqiang ChenDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Caixia LiangDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Manyu ChenDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Qiulong LiuDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Zhihao LiDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Jierong XieDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Zhennan WangDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Sihai LiaoDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.
Yufang ZuoDepartment of Gynecologic and Genitourinary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study evaluated efficacy and safety of concurrent chemoradiotherapy (CCRT) versus CCRT plus adjuvant chemotherapy (CCRT+ACT) in 2018 Federation International of Gynecology and Obstetrics (FIGO) Stage III locally advanced cervical cancer (LACC) patients. This study provides clinical evidence to optimize treatment strategies for stage III LACC.

methodsA total of 72 patients diagnosed with stage III LACC were retrospectively enrolled from the Cancer Hospital of Guangdong Medical University between May 2018 and May 2024. They were divided into the CCRT group (n = 33) and the CCRT+ACT group (n = 39). Survival endpoints were analyzed using the Kaplan-Meier method with log-rank tests, and Cox proportional hazards regression models were applied to identify prognostic factors.

resultsThe 3-year OS (79.5% vs. 63.6%,P = 0.238) and PFS (56.4% vs. 45.5%,P = 0.706) rates showed no significant differences between the CCRT+ACT and CCRT groups. Kaplan-Meier survival analysis suggested that a positive lymph node size ≥ 10 mm (relative to a < 10 mm reference) may be associated with an increased hazard for mortality (HR = 8.235; P = 0.020) and disease progression (HR = 2.986; P = 0.020). Furthermore, abnormal post-brachytherapy SCC-Ag levels (> 1.5 ng/mL vs. ≤ 1.5 ng/mL reference) appeared to be strongly linked to adverse OS (HR = 13.641; P < 0.001) and PFS (HR = 4.722; P = 0.007). Regarding safety, CCRT+ACT did not increase grade 3-4 toxicities, suggesting a manageable safety profile.

conclusionWhile CCRT+ACT did not significantly improve survival in the un-selected stage III LACC population, a positive lymph node size of ≥ 10 mm and elevated post-brachytherapy SCC-Ag levels may serve as important prognostic indicators for adverse outcomes. These findings are hypothesis-generating, suggesting that integrating these factors into clinical risk assessment might aid in refining the identification of high-risk subsets who could potentially benefit from more personalized, intensified adjuvant strategies in future prospective trials.

Indexed as

ChemoradiotherapyUterine Cervical NeoplasmsAdultChemotherapy, AdjuvantFemaleHumansMiddle AgedNeoplasm StagingPrognosisRetrospective StudiesTreatment Outcome

Identifiers

PMID42574435
PMCPMC13456255

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.