Evidence map›Paper›PMID 39877028›Full record

ArticleJTO clinical and research reports2025

Durvalumab, Tremelimumab, and Platinum Chemotherapy in

Chee Khoon Lee, Bin-Chi Liao, Shalini Subramaniam, Chao-Hua Chiu, Antony J Mersiades, Chao-Chi Ho, Chris Brown, Chun-Liang Lai, Brett G M Hughes, Tsung-Ying Yang and 15 more

Abstract read
In one paragraph

Article in JTO clinical and research reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Durvalumab Plus Chemotherapy in Patients WithJTO clinical and research reports · 2026
    Article
  3. Immune Doublet Checkpoint Inhibition inJTO clinical and research reports · 2026
    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

25 authors.

Chee Khoon LeeNHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
Bin-Chi LiaoNational Taiwan University Hospital, Taipei, Taiwan.
Shalini SubramaniamNHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
Chao-Hua ChiuTaipei Cancer Center and Taipei Medical University Hospital, Taipei, Taiwan.
Antony J MersiadesNHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
Chao-Chi HoNational Taiwan University Hospital, Taipei, Taiwan.
Chris BrownNHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
Chun-Liang LaiDalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Chiayi, Taiwan.
Brett G M HughesThe Prince Charles Hospital, Brisbane, Australia.
Tsung-Ying YangTaichung Veterans General Hospital, Taichung, Taiwan.
Ken O'ByrneQueensland University of Technology, Brisbane, Australia.
Yung-Hung LuoTaipei Veterans General Hospital, Taipei, Taiwan.
Sonia YipNHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
Ching-Liang HoTri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Victoria BrayLiverpool Hospital, Sydney, Australia.
Wu-Chou SuNational Cheng Kung University Hospital, Tainan, Taiwan.
Melissa MooreSt Vincent's Melbourne Hospital, Melbourne, Australia.
Wei-Lien FengNational Health Research Institutes, Miaoli, Taiwan.
Ya-Ying BaiNational Taiwan University Hospital, Taipei, Taiwan.
Kate FordNHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
Michelle M CumminsNHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
Martin R StocklerNHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
Benjamin J SolomonPeter MacCallum Cancer Centre, Melbourne, Australia.
Thomas JohnPeter MacCallum Cancer Centre, Melbourne, Australia.
James Chih-Hsin YangNational Taiwan University Hospital, Taipei, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Methods: Participants were treated with induction durvalumab, tremelimumab, and platinum-pemetrexed, followed by durvalumab-pemetrexed maintenance. Participants were divided into two cohorts: (1) Results: One hundred participants from Australia and Taiwan were enrolled. Median follow-up was 26 months with 88% and 96% experiencing progression events for T790M- and T790M+, respectively. The ORR for T790M- was 31% (95% confidence interval: 20-45), including two complete responses. The ORR for T790M+ was 21% (95% confidence interval: 12-34). Median durations of response were 9.5 months and 6.3 months for T790M- and T790M+, respectively; median progression-free survival rates were 6.5 months and 4.9 months, respectively. For T790M-, ORR was 27% for 50% or higher PD-L1 (n = 22) and 0% for less than 50% PD-L1 (n = 10), respectively. For T790M+, ORR was 17% for 50% or higher PD-L1 (n = 24). The safety profile was consistent with previous reports. Conclusions: Durvalumab, tremelimumab, and platinum-pemetrexed had modest anti-tumor activity in

Indexed as

Checkpoint inhibitorsChemotherapyEGFR mutationNon-small cell lung cancer

Identifiers

PMID39877028
PMCPMC11773228

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

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.