Evidence map›Paper›PMID 40386585›Full record

ArticleJournal of gastrointestinal oncology2025

Efficacy observation of sequential TAS-102 following regorafenib as a later-line treatment in patients with metastatic colorectal cancer: a cohort study.

Chang Xu, Xiangyu Cheng, Changqing Liu, Jing Ren, Vishal G Shelat, Timothy Price, José María Sayagués, Yi Gai, Guangyu Wang, Yusheng Wang

Abstract read
In one paragraph

Article in Journal of gastrointestinal oncology, 2025. 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

10 authors.

Chang Xu *Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.ORCID https://orcid.org/0009-0002-7798-6907
Xiangyu Cheng *Shanxi Medical University, Taiyuan, China.
Changqing Liu *Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
Jing RenDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.ORCID https://orcid.org/0009-0005-9787-3100
Vishal G ShelatDepartment of General Surgery, Tan Tock Seng Hospital, Singapore, Singapore.
Timothy PriceDepartment of Medical Oncology, The Queen Elizabeth Hospital, Woodville, Australia.
José María SayaguésPathology Service, Hospital Clínico Universitario de Salamanca and Biomedical Research Institute of Salamanca (IBSAL), University of Salamanca, Salamanca, Spain.
Yi GaiDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
Guangyu Wang *Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.ORCID https://orcid.org/0000-0002-8171-515X
Yusheng Wang *Department of Oncology Digestive, First Hospital of Shanxi Medical University, Taiyuan, China.ORCID https://orcid.org/0000-0002-9681-2876

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Metastatic colorectal cancer (mCRC) is associated with poor prognosis and limited options for later-line treatment. Regorafenib and TAS-102 have shown significant benefit and are recommended as later-line treatment for mCRC. This study aimed to investigate the progression-free survival (PFS) and overall survival (OS) of patients with mCRC treated with TAS-102 sequentially after regorafenib progression. Methods: This population-based cohort study retrospectively collected data of 30 patients with mCRC treated with TAS-102 sequentially after regorafenib at the Harbin Medical University Cancer Hospital and the Cancer Hospital Affiliated to Shanxi Medical University from January 1, 2020, to October 1, 2023. PFS and OS were considered to be the endpoints of this study. Kaplan-Meier analysis, log-rank test, and Cox proportional hazards regression analysis were used to analyze the OS, PFS, and risk factors. Results: Among the 30 patients included in the study, the median PFS (mPFS) for all patients was 3.83 months [95% confidence interval (CI): 3.09-5.59]. OS was divided into two categories: OS Conclusions: Our study demonstrated that the availability of sequential treatment options including regorafenib followed by TAS-102 prolongs the OS of patients compared to conventional monotherapy approaches. During the sequential treatment, regorafenib or TAS-102 combined with other therapeutic agents did not significantly differ from monotherapy, further investigation is required through large-scale trials.

Indexed as

later-line treatmentMetastatic colorectal cancer (mCRC)regorafenibsequentialTAS-102

Identifiers

PMID40386585
PMCPMC12078804

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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.