Evidence map›Paper›PMID 41355609›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Rapid Microfluidic Drug Sensitivity Testing Within 5 Days Using Minimal Clinical Tumor Samples.

Yi-Xue Chen, Yi Zhang, Yu-Jie Yan, Meng-Ting Zhang, Jian-Bo Chen, Yi-Rong Jiang, Jie Wu, Hui-Feng Wang, Jian-Zhang Pan, Zhi-Gang Chen and 2 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

12 authors.

Yi-Xue ChenInstitute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Yi ZhangDepartment of Breast Surgery (Surgical Oncology), Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310009, China.
Yu-Jie YanKey Laboratory of Tumor Microenvironment and Immune Therapy of Zhejiang Province, Hangzhou, 310052, China.
Meng-Ting ZhangInstitute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Jian-Bo ChenInstitute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Yi-Rong JiangInstitute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Jie WuInstitute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Hui-Feng WangInstitute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Jian-Zhang PanInstitute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Zhi-Gang ChenDepartment of Breast Surgery (Surgical Oncology), Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310009, China.
Jian HuangDepartment of Breast Surgery (Surgical Oncology), Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310009, China.
Qun FangInstitute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.ORCID https://orcid.org/0000-0002-6250-252X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rapid screening of personalized drugs based on patients' primary cell samples can provide precise and timely treatment guidance for clinical oncology patients. However, this goal faces great challenges due to the scarce clinical samples and large sample consumption, and long experimental time required by current drug screening methods. Here, a rapid, high-throughput microfluidic drug sensitivity testing system capable of accomplishing single and combination drug screening of multiple antitumor drugs in 5 days is established with minimal amounts of clinical primary tumor samples, avoiding the need for cell pre-expansion and preserving the tumor heterogeneity. An airflow-impacting approach is developed to fabricate nanoliter-scale microcavity arrays with ultra-smooth microcavity surfaces, with which rapid formation and 3D culture of tumor cell spheroids from small numbers of cell samples, as well as the subsequent high-throughput drug sensitivity testing can be achieved within 5 days. This applies the system in rapid drug sensitivity testing on primary samples from 21 clinical breast cancer patients to quantify the responses of patient-derived cells to chemotherapy and endocrine drugs under both the mono-drug and combinational-drug treatment modes.

Indexed as

Antineoplastic AgentsBreast NeoplasmsMicrofluidic Analytical TechniquesMicrofluidicsCell Line, TumorDrug Screening Assays, AntitumorFemaleHigh-Throughput Screening AssaysHumansSpheroids, CellularAntineoplastic Agents3D cell culturehigh‐throughput drug screeningmicrofluidicsorgans‐on‐a‐chippersonalized therapy

Identifiers

PMID41355609
PMCPMC12903994

What OpenQuestion holds

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Registered trials

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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.