Evidence map›Paper›PMID 41062089›Full record

ArticleCancer reports (Hoboken, N.J.)2025

Long-Term Outcomes and Toxicities in Patients With Metastatic Non-Small Cell Lung Cancer Treated With Immunotherapy Containing Regimens.

Meghana Maddula, Lauren J Brown, Venessa Chin, Bo Gao, Ines Pires Da Silva, Adnan Nagrial

Abstract readMulticenter Study
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 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. 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

6 authors.

Meghana MaddulaCrown Princess Mary Cancer Centre, Westmead Hospital, Sydney, New South Wales, Australia.ORCID 0009-0003-4819-9397
Lauren J BrownCrown Princess Mary Cancer Centre, Westmead Hospital, Sydney, New South Wales, Australia.ORCID 0000-0002-9340-8392
Venessa ChinUniversity of New South Wales, Sydney, New South Wales, Australia.ORCID 0000-0002-4630-4451
Bo GaoCrown Princess Mary Cancer Centre, Westmead Hospital, Sydney, New South Wales, Australia.ORCID 0000-0002-7881-6603
Ines Pires Da SilvaMedical Oncology, Blacktown Hospital, Sydney, New South Wales, Australia.ORCID 0000-0003-3540-8906
Adnan NagrialCrown Princess Mary Cancer Centre, Westmead Hospital, Sydney, New South Wales, Australia.ORCID 0000-0003-0275-2479

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionImmunotherapy is well-established in treating metastatic non-small cell lung cancer (mNSCLC); however, data regarding acquired resistance and long-term outcomes are limited. We examined long-term outcomes in mNSCLC patients with ongoing treatment response at 2 years (long-term responders) post-treatment commencement.

methodsThis multi-center retrospective study identified mNSCLC patients treated with first- or second-line immunotherapy±chemotherapy. Endpoints included progression-free survival (PFS) and overall survival (OS), stratified by PD-L1 tumor proportion score (TPS) (< 50% vs. ≥ 50%), treatment duration, and treatment line.

resultsOf 354 patients, 52 (15%) long-term responders were identified for analysis. Among them, median age was 68.5 years (28-87); the majority had an ECOG performance status ≤ 1 (81%), high-PD-L1 TPS (52%), and adenocarcinoma histopathology (83%). Most (73%) received immunotherapy first-line. Median treatment duration was 23.5 months (1-80), and 19% prematurely ceased treatment. With a median follow-up of 39 months from treatment commencement (95% CI 37-49), 15 (29%) patients had progressive disease, and 3-year PFS was 78%. Oligo-progression was common (87%), with lung/pleural disease (53%). Most received subsequent treatment (local therapy alone: 53%, systemic therapy alone: 20%, combined: 20%, supportive care: 7%) and achieved disease control (86%). Long-term toxicities occurred in 44% and were predominantly endocrinopathies (83%) requiring ongoing management. Three-year OS was 93%. Survival outcomes were unaffected by treatment duration, PD-L1 TPS, and treatment line.

conclusionsLong-term responders showed favorable survival outcomes, with most maintaining disease control with local therapies even after progression. This held true regardless of treatment duration, PD-L1 TPS, or treatment line. Endocrinopathies were common long-term toxicities.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsImmunotherapyLung NeoplasmsAdultAgedAged, 80 and overB7-H1 AntigenFemaleHumansMaleMiddle AgedProgression-Free SurvivalRetrospective StudiesTreatment OutcomeB7-H1 AntigenCD274 protein, humanImmune Checkpoint Inhibitorsimmunotherapyimmunotherapy related adverse eventslung neoplasmsnon‐small cell lung carcinomareal‐world data

Identifiers

PMID41062089
PMCPMC12507465

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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.