Evidence map›Paper›PMID 41737987›Full record

ArticleDrug design, development and therapy2026

Real-World Outcomes and Safety of PD-1 Blockade Rechallenge Strategies After Prior Immunotherapy in Advanced NSCLC: A Retrospective Cohort Study.

Ling-Jie Zheng, Yan-Li Shen, Hong-Wei Zhao, Yong-Cheng Ma, Ai-Feng Wang

Abstract read
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Article in Drug design, development and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ling-Jie ZhengDepartment of Pharmacy, Fuwai Central China Cardiovascular Hospital, Central China Fuwai Hospital of Zhengzhou University, Henan Key Laboratory of Individualized Drug Therapy for Cardiovascular Diseases, Zhengzhou, Henan, 450046, People's Republic of China.
Yan-Li ShenDepartment of Respiratory Medicine, Fuwai Central China Cardiovascular Hospital, Central China Fuwai Hospital of Zhengzhou University, Zhengzhou, Henan, 450046, People's Republic of China.
Hong-Wei ZhaoDepartment of Pharmacy, Fuwai Central China Cardiovascular Hospital, Central China Fuwai Hospital of Zhengzhou University, Henan Key Laboratory of Individualized Drug Therapy for Cardiovascular Diseases, Zhengzhou, Henan, 450046, People's Republic of China.
Yong-Cheng MaDepartment of Pharmacy, Fuwai Central China Cardiovascular Hospital, Central China Fuwai Hospital of Zhengzhou University, Henan Key Laboratory of Individualized Drug Therapy for Cardiovascular Diseases, Zhengzhou, Henan, 450046, People's Republic of China.
Ai-Feng WangDepartment of Pharmacy, Fuwai Central China Cardiovascular Hospital, Central China Fuwai Hospital of Zhengzhou University, Henan Key Laboratory of Individualized Drug Therapy for Cardiovascular Diseases, Zhengzhou, Henan, 450046, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Evidence to guide treatment after progression on immunotherapy remains limited in advanced non-small cell lung cancer (NSCLC). We descriptively report real-world outcomes of two PD-1 rechallenge strategies (PD-1 plus chemotherapy and PD-1 plus anlotinib) using a contemporaneous docetaxel cohort as contextual reference. Methods: Patients with advanced NSCLC who failed prior immunotherapy were screened retrospectively, 33 patients received PD-1 blockade plus chemotherapy, 31 received PD-1 blockade plus anlotinib and 63 patients treated with docetaxel monotherapy were served as a contextual reference cohort. Outcomes including objective response rate (ORR), disease control rate (DCR), duration of response (DoR), progression-free survival (PFS), overall survival (OS), and treatment-related adverse events (TRAEs) were summarized by cohort. Survival outcomes were estimated using Kaplan-Meier methods. Results: ORR and DCR were 30.3% (95% CI: 15.6%-48.7%) and 84.8% (95% CI: 68.1%-94.9%) in PD-1 plus chemotherapy cohort, 22.6% (95% CI: 9.6%-41.1%) and 80.6% (95% CI: 62.5%-92.5%) in PD-1 plus anlotinib cohort, 15.9% (95% CI: 7.9%-27.3%) and 54.0% (95% CI: 40.9%-66.6%) in docetaxel cohort. Median DoR among responders was 6.9 months (95% CI: 0.7-13.1), 7.1 months (95% CI: 5.0-9.2), and 3.1 months (95% CI: 1.9-4.3), respectively. Median PFS was 7.0 months (95% CI: 0.7-13.3), 6.5 months (95% CI: 2.2-10.8), and 3.3 months (95% CI: 2.2-4.4), and median OS was 17.8 months (95% CI: 8.0-27.6), 16.8 months (95% CI: 13.9-19.7), and 9.5 months (95% CI: 4.8-14.2), respectively. Any-grade TRAEs occurred in 84.8%, 80.6%, and 81.0%, and grade ≥3 TRAEs were 42.4%, 41.9%, and 34.9%, respectively. No treatment-related deaths were observed. Conclusion: PD-1 rechallenge strategies showed measurable antitumor activity and manageable safety profile in a subset of previously immunotherapy-treated advanced NSCLC. Limitations existed in this study and the findings were descriptive and hypothesis-generating and should be interpreted cautiously because treatment selection was non-random and important confounders might be incompletely captured.

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsImmunotherapyLung NeoplasmsProgrammed Cell Death 1 ReceptorAgedCohort StudiesDocetaxelFemaleHumansIndolesMaleMiddle AgedQuinolinesRetrospective StudiesanlotinibAntineoplastic AgentsDocetaxelImmune Checkpoint InhibitorsIndolesPDCD1 protein, humanProgrammed Cell Death 1 ReceptorQuinolinesanlotinibchemotherapydocetaxelnon-small cell lung cancerPD-1 blockadepreviously immunotherapy-treatedsafetytherapeutic outcomes

Identifiers

PMID41737987
PMCPMC12927776

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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.