Evidence map›Paper›PMID 41732659›Full record

ArticleTherapeutic advances in medical oncology2026

Induction chemotherapy administration increases the risk of radiation pneumonitis in unresectable stage III NSCLC patients undergoing concurrent chemoradiotherapy with immunotherapy.

Pengwei Li, Yiwei Qin, Xinyi Liang, You Mo, Dawei Chen

Abstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2026. 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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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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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

5 authors.

Pengwei LiDepartment of Shandong Provincial Key Laboratory of Precision Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, People's Republic China.ORCID https://orcid.org/0009-0003-4037-8569
Yiwei QinDepartment of Shandong Provincial Key Laboratory of Precision Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, People's Republic of China.ORCID https://orcid.org/0009-0001-1871-4699
Xinyi LiangDepartment of Shandong Provincial Key Laboratory of Precision Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, People's Republic China.ORCID https://orcid.org/0009-0004-6610-1207
You MoDepartment of Cardiovascular Medicine, The First Affiliated Hospital of Shantou University Medical College, Shantou University, Shantou, Guangdong 515000, People's Republic of China.ORCID https://orcid.org/0000-0001-5283-0741
Dawei ChenDepartment of Shandong Provincial Key Laboratory of Precision Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, No. 440, Jiyan Road, Huaiyin District, Jinan, Shandong 250000, People's Republic of China.ORCID https://orcid.org/0000-0002-6762-7997

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Concurrent chemoradiotherapy (cCRT) is essential for stage III unresectable non-small cell lung cancer (NSCLC) but increases the risk of radiation pneumonitis (RP), especially with immunotherapy (IO). Induction chemotherapy (ICT) controls tumor progression but damages lung tissue, raising RP risk. Research on the RP risk from ICT, cCRT, and IO consolidation is poorly investigated. Objectives: We evaluated whether ICT increases RP incidence and affects survival in the IO era. Design: This was a retrospective analysis conducted at a single cancer center. Methods: Retrospective data from stage III unresectable NSCLC patients treated with cCRT and IO between 2018 and 2024 were analyzed. Patients were divided into cCRT without ICT ( Results: The ICT before cCRT group showed a higher incidence of ⩾Grade 2 RP compared to the cCRT without ICT group (Gray's test, SHR = 1.964, 95% confidence interval (CI): 1.137-3.394, Conclusion: ICT followed by cCRT showed a higher incidence of ⩾Grade 2 RP compared to cCRT alone in patients with unresectable stage III NSCLC receiving consolidation immunotherapy.

Indexed as

concurrent chemoradiotherapyinduction chemotherapynon-small cell lung cancerradiation pneumonitisstage III NSCLC

Identifiers

PMID41732659
PMCPMC12924971

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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.