Evidence map›Paper›PMID 41423267›Full record

ArticleJournal for immunotherapy of cancer2025

Multi-omics analysis reveals differential benefits of immunotherapy±chemotherapy based on detailed smoking history in advanced non-small cell lung cancer.

Xinan Wang, Biagio Ricciuti, Arielle Elkrief, Joao V Alessi, Alessandro Di Federico, Federica Pecci, Mizuki Nishino, Doga Gulhan, Guruprasad Ananda, Scott J Rodig and 6 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. 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. Role of ctDNA Tumor Fraction in Selecting Immunotherapy-Based Regimens in Advanced Non-Small Cell Lung Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  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

16 authors.

Xinan WangDepartment of Biostatistics, Harvard T H Chan School of Public Health, Boston, Massachusetts, USA.ORCID http://orcid.org/0000-0001-5236-1105
Biagio RicciutiLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.ORCID http://orcid.org/0000-0002-0651-2678
Arielle ElkriefMemorial Sloan Kettering Cancer Center, New York, New York, USA.
Joao V AlessiLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Alessandro Di FedericoLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Federica PecciLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Mizuki NishinoLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Doga GulhanMassachusetts General Hospital, Boston, Massachusetts, USA.
Guruprasad AnandaDepartment of Data Science, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Scott J RodigBrigham and Women's Hospital, Boston, Massachusetts, USA.
Lynette ShollBrigham and Women's Hospital, Boston, Massachusetts, USA.
Bruce JohnsonLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Xihong LinDepartment of Biostatistics, Harvard T H Chan School of Public Health, Boston, Massachusetts, USA.
Adam SchoenfeldMemorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID http://orcid.org/0000-0002-2644-1416
Mark M AwadLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
David ChristianiDepartment of Environmental Health, Harvard T H Chan School of Public Health, Boston, Massachusetts, USA dchris@hsph.harvard.edu.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
The Boston Lung Cancer Survival CohortU01CA209414 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI David C Christiani · 2017 to 2026
$12.2M
Statistical Methods for Analysis of Massive Genetic and Genomic Data in Cancer ResearchR35CA197449 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI XIHONG LIN · 2015 to 2026
$10.9M
Human leukocyte antigen and immune response in non-small cell lung cancer: A multi-omics approachK99CA297010 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Xinan Wang · 2025 to 2026
$248k
NCI NIH HHS K99 CA297010NCI NIH HHS P30 CA008748NCI NIH HHS R35 CA197449NCI NIH HHS U01 CA209414
6 · The paper itself

Abstract

backgroundDespite immunotherapy±chemotherapy has transformed the therapeutic landscape for patients with non-small cell lung cancer (NSCLC), critical questions remain regarding how detailed smoking history affects the evolving treatment options and the underlying molecular mechanisms driving these effects.

methodsWe analyzed 4157 patients with advanced NSCLC who were treated with immunotherapy monotherapy (IO alone) (n=2768) or chemoimmunotherapy (chemo-IO) (n=1389) at the Dana-Farber Cancer Institute and Memorial Sloan Kettering Cancer Center (2010-2023). Associations between detailed smoking history (status and cumulative pack-years) and clinical outcomes were assessed using multivariable analyses. First-line chemo-IO versus IO alone was compared in programmed death receptor ligand 1 (PD-L1) Tumor Proportion Score (TPS) of ≥50%

resultsIn patients receiving IO alone, both smoking status and intensity showed dose-dependent associations with improved response and survival outcomes. In contrast, among patients receiving chemo-IO, smoking history did not affect initial response but patients with active (HR=0.73, 95% CI 0.57 to 0.94, p=0.01) and heavy tobacco use (HR=0.76, 95% CI 0.62 to 0.93, p=0.001) showed improved progression-free survival (PFS), and a trend toward improved overall survival (OS). Importantly, these associations remained independent of

conclusionsDetailed smoking history provides crucial insights for optimizing IO selection in advanced NSCLC through mechanistic alterations in both the tumor microenvironment and systemic plasma protein profiles.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungImmunotherapyLung NeoplasmsMultiomicsTobacco SmokingAgedCohort StudiesFemaleHumansLymphocytes, Tumor-InfiltratingMaleMultivariate AnalysisPatient SelectionTumor MicroenvironmentBiomarkerImmunotherapyNon-Small Cell Lung CancerTumor infiltrating lymphocyte - TILTumor mutation burden - TMB

Identifiers

PMID41423267
PMCPMC12719888

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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.