Evidence map›Paper›PMID 41409455›Full record

ArticleClinical Medicine Insights. Oncology2025

Predictive Value of Patient-Derived Tumor Cell Cluster-Based Drug Sensitivity Assay in Advanced NSCLC.

Yangchun Gu, Leilei Yang, Hua Zhang, Shenyi Yin, Lu Yang, Zhentao Liu, Jinyu Yu, Huiying Huang, Juan Li, Baoshan Cao

Abstract read
In one paragraph

Article in Clinical Medicine Insights. 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.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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.

Yangchun GuDepartment of Medical Oncology and Radiation Sickness, Peking University Third Hospital, Beijing, China.ORCID https://orcid.org/0000-0003-3278-7285
Leilei YangGeneX Health Co., Ltd., Beijing, China.
Hua ZhangResearch Center of Clinical Epidemiology, Peking University Third Hospital, Beijing, China.
Shenyi YinGeneX Health Co., Ltd., Beijing, China.
Lu YangDepartment of Medical Oncology and Radiation Sickness, Peking University Third Hospital, Beijing, China.
Zhentao LiuDepartment of Medical Oncology and Radiation Sickness, Peking University Third Hospital, Beijing, China.
Jinyu YuDepartment of Medical Oncology and Radiation Sickness, Peking University Third Hospital, Beijing, China.
Huiying HuangDepartment of Medical Oncology and Radiation Sickness, Peking University Third Hospital, Beijing, China.
Juan LiState Key Laboratory of Natural and Biomimetic Drugs, Department of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.
Baoshan CaoDepartment of Medical Oncology and Radiation Sickness, Peking University Third Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Patient-derived tumor cell cluster (PTC)-based drug sensitivity assays show promise for enabling precision drug selection; however, their predictive value in advanced non-small cell lung cancer (NSCLC) requires further elucidation. Methods: To assess the concordance between PTC-based drug sensitivity and clinical outcomes, we conducted a single-center prospective cohort study at Peking University Third Hospital from August 2021 to August 2024. We enrolled 38 consecutive patients, from whom 44 fresh tumor specimens were obtained for PTC-based drug sensitivity assays and compared with paired clinical outcomes of chemotherapy and targeted therapy regimens. Concordance was assessed using the Kappa statistic and receiver operating characteristic curve analysis. A Cox proportional-hazard model was used to identify prognostic factors for progression-free survival (PFS). Results: We observed an 81.8% (36/44) concordance between the PTC killing rate (>0% vs 0%) and the best overall clinical response (disease controlled vs disease progression per RECIST v1.1) (Kappa = 0.484, area under the curve (AUC) = 0.740). The concordance with the local response of the biopsied lesions was even higher, at 87.5% (35/40) (Kappa = 0.593, AUC = 0.841). A PTC killing rate >0% was correlated with significantly longer PFS (8.6 vs 2.0 months, Conclusions: These findings validate the predictive value of the PTC-based drug sensitivity assay in guiding personalized treatment for patients with advanced NSCLC and support its clinical translation. Registration: Chinese Clinical Trial Registry, Registration No.: ChiCTR2100048791, https://www.chictr.org.cn/showproj.html?proj=129885.

Indexed as

3-dimensional cell spheroidin vitro drug sensitivity assaynon-small cell lung cancer (NSCLC)patient-derived tumor cell cluster (PTC)progression-free survival (PFS)

Identifiers

PMID41409455
PMCPMC12705941

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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.