Evidence map›Paper›PMID 42729373›Full record

ArticleFrontiers in immunology2026

Impact of time-of-day and timing interval of neoadjuvant immunotherapy and chemotherapy infusions among patients with operable NSCLC using the inverse probability of treatment weighting method: a dual-center, retrospective study.

Xiang-Yang Yu, Wen-Yu Zhai, Zheng-Zheng Xia, Kai Ma, Bai-Hua Zhang, Xin Yu, Sheng-Cheng Lin, Xiao-Tong Guo, Ze-Rui Zhao, Zhen-Tao Yu

Abstract readMulticenter Study
In one paragraph

Article 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
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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

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Xiang-Yang Yu *Department of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Wen-Yu Zhai *Department of Thoracic Surgery, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, China.
Zheng-Zheng Xia *Department of Pharmacy, National Cancer Center/National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Kai MaDepartment of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Bai-Hua ZhangDepartment of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Xin YuDepartment of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Sheng-Cheng LinDepartment of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Xiao-Tong GuoDepartment of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Ze-Rui ZhaoDepartment of Thoracic Surgery, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, China.
Zhen-Tao YuDepartment of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer, Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Although multiple studies have confirmed that adjusting the time-of-day (ToDA) of immunotherapy and timing interval (TI) of chemoimmunotherapy can improve long-term outcomes in patients with advanced non-small cell lung cancer (NSCLC), whether this model similarly improves survival among patients with operable NSCLC has not been reported. Patients and methods: This dual-center, retrospective study included adult patients who received neoadjuvant chemoimmunotherapy (neoCIT) for clinical stage T1-4N0-3M0 NSCLC between January 2019 and December 2024. The impact of the ToDA of neoadjuvant immunotherapy (neoIO) on the efficacy and safety were analyzed. In addition, the inverse probability of treatment weighting (IPTW)-weighted Cox regression model was used to compare disease-free survival (DFS) and overall survival (OS) between patients who received either ≥75% (≥75% group) or <75% (<75% group) of the neoIO administrations before 14:00 h. Results: A total of 168 consecutive patients with a median follow-up of 30.3 months were included, of whom 123 patients (73.2%) were in the ≥75% group. Neoadjuvant treatment-related adverse events (neoTRAEs) occurred in 47.6% of the patients, including 63 (51.2%) and 17 (37.8%) patients in the ≥75% and <75% groups, respectively ( Conclusions: Although early infusions of most neoIO drugs did not affect safety or efficacy, it showed a potential trend toward improving long-term survival. The corresponding immune microenvironment and molecular mechanisms need further exploration to guide the design of future prospective clinical studies.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungImmunotherapyLung NeoplasmsNeoadjuvant TherapyAgedFemaleHumansMaleMiddle AgedNeoplasm StagingRetrospective StudiesTime FactorsTreatment Outcomeneoadjuvant immunotherapynon-small cell lung cancerprognosistime-of-daytiming interval

Identifiers

PMID42729373
PMCPMC13561947

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