Evidence map›Paper›PMID 41743719›Full record

SynthesisFrontiers in immunology2026

What determines value? Exploring value characteristics of novel therapies for digestive system cancers.

Shunlong Ou, Song Wang, Xiaoyi Chen, Huan Li, Chengyang Zhou, Qian Jiang

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in immunology, 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

6 authors.

Shunlong Ou *Department of Pharmacy, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu, China.
Song Wang *Department of Pharmacy, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu, China.
Xiaoyi ChenSchool of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Huan LiSchool of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Chengyang ZhouDepartment of Pharmacy, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu, China.
Qian JiangDepartment of Pharmacy, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Despite the growing arsenal of novel anti-tumor drugs for digestive system cancers, concerns persist regarding their true clinical value, as approvals often rely on surrogate endpoints with limited overall survival or quality of life data. This study systematically evaluates the clinical benefit of these drugs in China using standardized value assessment frameworks and identify factors associated with high-value treatments. Methods: This cross-sectional study analyzed 65 indications from 33 novel anti-tumor drugs included in the Guidelines for the Clinical Application of Novel Anti-tumor Drugs for advanced digestive system cancers. Two researchers independently extracted data from drug approval documents and PubMed literature. Value assessment was performed using ASCO Value Framework v2.0 (advanced disease) and ESMO-Magnitude of Clinical Benefit Scale v2.0 (non-curative). For ASCO-VF, the net health benefit score was calculated based on clinical benefit, toxicity adjustments, and bonus points. ESMO-MCBS grading incorporated clinical benefit magnitude with adjustments for toxicity and quality of life. Statistical analyses included descriptive statistics and association testing with odds ratios for categorical variables. Results: Among 65 indications, only 12 (18.5%) achieved value thresholds in both frameworks. Immune combinations showed superior value, particularly atezolizumab-bevacizumab in hepatocellular carcinoma (ASCO-VF: 53.4; ESMO-MCBS: grade 5) and toripalimab in esophageal squamous cell carcinoma. Quality of life improvement strongly correlated with value attainment in both frameworks (ASCO-VF OR: 28.00; ESMO-MCBS OR: 27.87). Molecular target detection requirement inversely associated with OS benefit (OR: 0.16). Value heterogeneity was observed across cancer types and treatment lines. Conclusions: Few novel digestive system cancer drugs demonstrate substantial clinical benefit in both value frameworks. Quality of life documentation is crucial for value assessment. Stakeholders should integrate these value dimensions-survival benefit, toxicity, and quality of life-into clinical and policy decisions to guide treatment selection and resource allocation.

Indexed as

ASCO-VFclinical benefitdigestive system cancersESMO-MCBSfactors associated valuenovel anti-tumor drugs

Identifiers

PMID41743719
PMCPMC12929542

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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.