Evidence map›Paper›PMID 42896976›Full record

ReviewZhongguo fei ai za zhi = Chinese journal of lung cancer2026

[Evolution of Perioperative Immunotherapy Paradigms in Non-small Cell Lung Cancer: From Adjuvant Dilemma to Neoadjuvant Priority].

Jie Xu, Zhansheng Jiang

Abstract readReviewEnglish Abstract
In one paragraph

Review in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 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

2 authors.

Jie XuDepartment of Thoracic Oncology II, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin Key Laboratory of Cancer Prevention and Therapy, Tianjin Clinical Research Center for Malignant Tumors, Tianjin Key Laboratory of Cancer Immunology and Biotherapy, Tianjin 300060, China.
Zhansheng JiangDepartment of Integrated Traditional Chinese and Western Medicine, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin Key Laboratory of Cancer Prevention and Therapy, Tianjin Clinical Research Center for Malignant Tumors, Tianjin Key Laboratory of Cancer Immunology and Biotherapy, Tianjin 300060, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The application of immune checkpoint inhibitors (ICIs) has reshaped the perioperative treatment pattern of resectable non-small cell lung cancer (NSCLC). Currently, three treatment paradigms have emerged: adjuvant, neoadjuvant alone, and 'sandwich' (neoadjuvant+surgery+adjuvant). Although IMpower010 and KEYNOTE-091 achieved positive results in adjuvant immunotherapy, the negative results of two large phase III studies, BR.31 and ANVIL, raised questions about the generalizability of this model. In contrast, neoadjuvant immunotherapy has shown efficacy in multiple phase III studies. This advantage may stem from the preservation of the intact tumor antigen repertoire and draining lymph node architecture, enabling chemo-immunotherapy to elicit more robust systemic immune responses. Currently, both neoadjuvant alone and 'sandwich' models are recommended by guidelines, but the 5-year overall survival (OS) rates of CheckMate-816 and KEYNOTE-671 are nearly identical (65.4% vs 64.6%), and the pathological complete response (pCR) rate of CheckMate-77T (25.3%) is comparable to that of CheckMate-816 (24%), suggesting that the incremental benefit of extending neoadjuvant cycles and adding postoperative adjuvant immunotherapy in the 'sandwich' model is very limited. In the future, an individualized decision-making model based on pCR and molecular residual disease (MRD) status, such as de-escalation to observation for those achieving pCR with negative MRD, and intensification for those with residual disease or positive MRD, is expected to optimize the balance between treatment intensity and survival benefit. In summary, the existing evidence favors the adoption of a 'neoadjuvant first' strategy for resectable NSCLC. Based mainly on cross-trial indirect comparisons, the neoadjuvant alone model offers comparable efficacy to the 'sandwich' approach with potential cost-effectiveness advantages, and may be preferred as the initial strategy. Individualized post-neoadjuvant management represents the future direction of this field.
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Indexed as

Carcinoma, Non-Small-Cell LungImmunotherapyLung NeoplasmsNeoadjuvant TherapyHumansPathologic Complete ResponseAdjuvant therapyImmunotherapyLung neoplasmsNeoadjuvant therapyTreatment pattern

Identifiers

PMID42896976
PMCPMC13688445

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.