Evidence map›Paper›PMID 41812622›Full record

Trial reportESMO open2026

A randomized phase III clinical trial of weekly versus tri-weekly cisplatin-based chemoradiotherapy for locally advanced cervical cancer: results of the TACO (GCIG/KGOG 1027/THAI 2012) study.

S Y Ryu, B H Nam, M H Kim, W I Jang, C Sitathanee, T D Linh, K H Lee, W M Lee, E T Kim, S B Kang and 17 more

Abstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in ESMO open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

27 authors.

S Y RyuDepartment of Gynecologic Oncology, Korea Institute of Radiological & Medical Science, Seoul, Republic of Korea. Electronic address: ryu@kcch.re.kr.
B H NamData Management Center, Korea Gynecologic Oncology Group, Seoul, Republic of Korea.
M H KimDepartment of Gynecologic Oncology, Korea Institute of Radiological & Medical Science, Seoul, Republic of Korea.
W I JangDepartment of Radiation Oncology, Korea Institute of Radiological & Medical Science, Seoul, Republic of Korea.
C SitathaneeDepartment of Radiation Oncology, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
T D LinhDepartment of Radiation Oncology, Ho Chi Minh City Oncology Hospital, Ho Chi Minh, Vietnam.
K H LeeDepartment of Obstetrics and Gynecology, Seoul St. Mary's Hospital, Catholic University, Seoul, Republic of Korea.
W M LeeDepartment of Obstetrics and Gynecology, Hanyang University, Seoul, Republic of Korea.
E T KimDepartment of Obstetrics and Gynecology, Kosin University Gospel Hospital, Busan, Republic of Korea.
S B KangDepartment of Obstetrics and Gynecology, Hosan Women's Hospital, Seoul, Republic of Korea.
J H KimDepartment of Obstetrics and Gynecology, Gangnam Severance Hospital, Yonsei University, Seoul, Republic of Korea.
J Y ParkDepartment of Obstetrics and Gynecology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
K B LeeDepartment of Obstetrics and Gynecology, Gachon University Gil Hospital, Incheon.
C H ChoDepartment of Obstetrics and Gynecology, Keimyung University, Daegu, Republic of Korea.
H LouDepartment of Obstetrics and Gynecology, Zheijiang Cancer Center, Hangzhou, China.
Y H KimDepartment of Obstetrics and Gynecology, Ewha Womans University College of Medicine, Seoul, Republic of Korea.
Y T KimDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Y H LeeDepartment of Obstetrics and Gynecology, Kyungpook National University College of Medicine, Daegu, Republic of Korea.
X WuDepartment of Gynecologic Oncology, Fudan University Cancer Institute, Shanghai, China.
J W KimDepartment of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Republic of Korea.
S I ParkDepartment of Obstetrics and Gynecology, Dongnam Institute of Radiological & Medical Science, Busan, Republic of Korea.
S JeonDepartment of Obstetrics and Gynecology, Soonchunhyang University Cheonan Hospital, Cheonan, Republic of Korea.
D H ThinhDepartment of Radiation Oncology, Ho Chi Minh City Oncology Hospital, Ho Chi Minh, Vietnam.
S F KryDepartment of Radiation Physics, IROC Houston QA Center, University of Texas MD Anderson Cancer Center, Houston.
D GaffneyDepartment of Radiation Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, USA.
W SmallDepartment of Radiation Oncology, Stritch School of Medicine, Loyola University Chicago, Chicago, USA.
S WilailakDepartment of Obstetrics and Gynecology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand. Electronic address: sarikapanw@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe standard treatment for locally advanced cervical cancer is cisplatin-based chemoradiotherapy; however, the optimal dose and dosing schedule of cisplatin remain debated. The aim of this study was to compare the clinical outcomes of weekly cisplatin at 40 mg/m PATIENTS AND

methodsIn this prospective, randomized clinical trial, we enrolled 314 patients with stage IIB-IVA cervical cancer, randomly assigning them in a 1 : 1 ratio into two arms. The weekly arm received a weekly dose of 40 mg/m

resultsChemotherapy delay was more frequent in the weekly arm than in the tri-weekly arm (P = 0.008). However, the 3-year recurrence-free survival rate between the two arms did not significantly differ (78.7% in the weekly arm, 84.1% in the tri-weekly arm; hazard ratio 0.71, 95% confidence interval 0.39-1.32, P = 0.28). The pattern of recurrence did not differ significantly between the two arms. Grade 3 and 4 hematological toxicities occurred less frequently in the tri-weekly arm (P < 0.001). Furthermore, the tri-weekly arm had better QOL scores across several domains compared with the weekly arm.

conclusionIn this study, tri-weekly cisplatin-based chemoradiotherapy was not statistically superior to a weekly schedule in terms of survival outcomes for patients with locally advanced cervical cancer. However, the tri-weekly regimen exhibited a more favorable toxicity profile and improved QOL compared with the weekly regimen. These results suggest tri-weekly cisplatin administration as a feasible alternative for chemoradiotherapy in cervical cancer.

Indexed as

Antineoplastic AgentsChemoradiotherapyCisplatinUterine Cervical NeoplasmsAdultAgedDrug Administration ScheduleFemaleHumansMiddle AgedProspective StudiesQuality of LifeAntineoplastic AgentsCisplatincervical cancerchemoradiotherapycisplatinquality of lifetri-weeklyweekly

Identifiers

PMID41812622
PMCPMC12995827

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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.