Evidence map›Paper›PMID 37801329›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2024

Durvalumab ± Tremelimumab + Platinum-Etoposide in Extensive-Stage Small Cell Lung Cancer (CASPIAN): Outcomes by PD-L1 Expression and Tissue Tumor Mutational Burden.

Luis Paz-Ares, Marina Chiara Garassino, Yuanbin Chen, Niels Reinmuth, Katsuyuki Hotta, Artem Poltoratskiy, Dmytro Trukhin, Maximilian J Hochmair, Mustafa Özgüroğlu, Jun Ho Ji and 12 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
12.2field-weighted citation impact, top 1% of its field
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

45 citing papers in PubMed, 53 citations in OpenAlex.

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  16. Phase I Dose-Escalation Trial Combining Olaparib and Thoracic Radiotherapy in Extensive-Stage Small Cell Lung Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 19 institutions in 14 countries.

Luis Paz-AresDepartment of Medical Oncology, Hospital Universitario 12 de Octubre, Lung Cancer Unit CNIO-H120, Complutense University and Ciberonc, Madrid, Spain.ORCID 0000-0002-1947-3364
Marina Chiara GarassinoFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-3821-5598
Yuanbin ChenCancer and Hematology Centers of Western Michigan, Grand Rapids, Michigan.ORCID 0009-0006-4175-8055
Niels ReinmuthAsklepios Lung Clinic, Member of the German Center for Lung Research (DZL), Munich-Gauting, Germany.ORCID 0000-0002-7369-4512
Katsuyuki HottaOkayama University Hospital, Okayama, Japan.ORCID 0000-0002-0112-0843
Artem PoltoratskiyPetrov Research Institute of Oncology, St. Petersburg, Russian Federation.ORCID 0000-0003-3259-2242
Dmytro TrukhinOdessa Regional Oncological Dispensary, Odessa, Ukraine.ORCID 0009-0006-3412-0758
Maximilian J HochmairKarl Landsteiner Institute of Lung Research and Pulmonary Oncology, Klinik Floridsdorf, Vienna, Austria.ORCID 0000-0002-8673-2450
Mustafa ÖzgüroğluIstanbul University-Cerrahpaşa, Cerrahpaşa School of Medicine, Istanbul, Turkey.ORCID 0000-0002-8417-8628
Jun Ho JiSamsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Republic of South Korea.ORCID 0000-0003-1730-2606
Galina StatsenkoOmsk Regional Cancer Center, Omsk, Russian Federation.ORCID 0000-0001-7123-8639
Nikolay ConevClinic of Medical Oncology, UMHAT St Marina, Varna, Bulgaria.ORCID 0000-0001-5267-0354
Igor BondarenkoDnipropetrovsk Medical Academy, Dnipro, Ukraine.ORCID 0000-0002-7071-2471
Libor HavelThomayer Hospital, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0009-0007-9131-226X
György LosonczySemmelweis University, Budapest, Hungary.ORCID 0000-0002-0211-5237
Mingchao XieAstraZeneca, Waltham, Massachusetts.ORCID 0009-0006-7061-5483
Zhongwu LaiAstraZeneca, Gaithersburg, Maryland.ORCID 0000-0002-1506-8222
Nadia Godin-HeymannAstraZeneca, Cambridge, United Kingdom.ORCID 0000-0003-3260-0302
Helen MannAstraZeneca, Cambridge, United Kingdom.ORCID 0000-0001-9426-2332
Haiyi JiangAstraZeneca, Gaithersburg, Maryland.ORCID 0009-0002-8677-6821
Yashaswi ShresthaAstraZeneca, Gaithersburg, Maryland.ORCID 0000-0002-5567-0277
Jonathan W GoldmanDavid Geffen School of Medicine at UCLA, Los Angeles, California.ORCID 0000-0002-4925-8243
AstraZeneca (Japan) · JPAstraZeneca (United Kingdom) · GBBudgetary Health Care Institution of the Omsk Region "Clinical Oncology Center" · RUCharles University · CZCity Clinical Oncology Center · RUDnipro State Medical University · UAGerman Center for Lung Research · DEHematology Oncology Consultants · USHospital Universitario 12 De Octubre · ESIstanbul University-Cerrahpaşa · TRKarl Landsteiner Society · ATMassachusetts Medical Society · USOkayama Shoka University · JPSemmelweis University · HUState Healthcare Institution "Regional Clinical Oncological Dispensary" · RUSungkyunkwan University · KRUniversity Hospital St. Marina · BGUniversity of California, Los Angeles · USUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn the CASPIAN trial, first-line durvalumab plus platinum-etoposide (EP) significantly improved overall survival (OS) versus EP alone in extensive-stage small cell lung cancer (ES-SCLC). We report exploratory analyses of CASPIAN outcomes by programmed cell death ligand-1 (PD-L1) expression and tissue tumor mutational burden (tTMB). EXPERIMENTAL

designPatients were randomized (1:1:1) to durvalumab (1,500 mg) plus EP, durvalumab plus tremelimumab (75 mg) plus EP, or EP alone. Treatment effects in PD-L1 and tTMB subgroups were estimated using an unstratified Cox proportional hazards model.

resultsThe PD-L1 and tTMB biomarker-evaluable populations (BEP) comprised 54.4% (438/805) and 35.2% (283/805) of the intention-to-treat population, respectively. PD-L1 prevalence was low: 5.7%, 25.8%, and 28.3% had PD-L1 expression on ≥1% tumor cells (TC), ≥1% immune cells (IC), and ≥1% TCs or ICs, respectively. OS benefit with durvalumab plus EP versus EP was similar across PD-L1 subgroups, with HRs all falling within the 95% confidence interval (CI) for the PD-L1 BEP (0.47‒0.79). OS benefit with durvalumab plus tremelimumab plus EP versus EP was greater in PD-L1 ≥1% versus <1% subgroups, although CIs overlapped. There was no evidence of an interaction between tTMB and treatment effect on OS (durvalumab plus EP vs. EP, P = 0.916; durvalumab plus tremelimumab plus EP vs. EP, P = 0.672).

conclusionsOS benefit with first-line durvalumab plus EP in patients with ES-SCLC was observed regardless of PD-L1 or tTMB status. PD-L1 expression may prove to be a useful biomarker for combined treatment with PD-(L)1 and CTLA-4 inhibition, although this requires confirmation with an independent dataset. See related commentary by Rolfo and Russo, p. 652.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedLung NeoplasmsSmall Cell Lung CarcinomaAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenEtoposideHumansPlatinumAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedB7-H1 AntigendurvalumabEtoposidePlatinumtremelimumab

Identifiers

PMID37801329
PMCPMC10870117
OpenAlexW4387391917

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.