Evidence map›Paper›PMID 35279527›Full record

Trial reportESMO open2022

Durvalumab, with or without tremelimumab, plus platinum-etoposide in first-line treatment of extensive-stage small-cell lung cancer: 3-year overall survival update from CASPIAN.

L Paz-Ares, Y Chen, N Reinmuth, K Hotta, D Trukhin, G Statsenko, M J Hochmair, M Özgüroğlu, J H Ji, M C Garassino and 11 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in ESMO open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05683977 (EvaluatioN of durvALumab Utilization and Effectiveness for First Line Extensive Stage Small Cell Lung Cancer. Prospective Cohort of Extensive Stage Small Cell Lung Cancer Patients Treated With Durvalumab Associated With Platinum-etoposide Chemotherapy), which is not on this map. Cited by 223 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
223citing papers in PubMed, 7 pooled it
29.0field-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.

NCT05683977 active not recruitingnot on this map

EvaluatioN of durvALumab Utilization and Effectiveness for First Line Extensive Stage Small Cell Lung Cancer. Prospective Cohort of Extensive Stage Small Cell Lung Cancer Patients Treated With Durvalumab Associated With Platinum-etoposide Chemotherapy

TypeobservationalSponsorAstraZenecaRan2022 to 2027Enrolled254ConditionsSmall Cell Lung CarcinomaArmsdurvalumab
3 · Its place in the literature

Who cites it

223 citing papers in PubMed, 7 syntheses or guidelines pooled it, 297 citations in OpenAlex.

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  19. RESILIENT Part 2: A Randomized, Open-Label Phase III Study of Liposomal Irinotecan Versus Topotecan in Adults With Relapsed Small Cell Lung Cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
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163 more citing papers are in PubMed but not listed here.

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

21 authors at 19 institutions in 14 countries.

L Paz-AresHospital Universitario 12 de Octubre, H12O-CNIO Lung Cancer Unit, Universidad Complutense and Ciberonc, Madrid, Spain. Electronic address: lpazaresr@seom.org.
Y ChenCancer & Hematology Centers of Western Michigan, Grand Rapids, USA.
N ReinmuthAsklepios Lung Clinic, Munich-Gauting, Germany.
K HottaOkayama University Hospital, Okayama, Japan.
D TrukhinOdessa Regional Oncological Dispensary, Odessa, Ukraine.
G StatsenkoOmsk Regional Cancer Center, Omsk, Russian Federation.
M J HochmairKarl Landsteiner Institute of Lung Research and Pulmonary Oncology, Krankenhaus Nord, Vienna, Austria.
M ÖzgüroğluIstanbul University-Cerrahpaşa, Cerrahpaşa School of Medicine, Istanbul, Turkey.
J H JiSamsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, South Korea.
M C GarassinoFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy; The University of Chicago Department of Medicine, Section of Hematology/Oncology, Chicago, USA.
O VoitkoKyiv City Clinical Oncological Centre, Kyiv, Ukraine.
A PoltoratskiyPetrov Research Institute of Oncology, St Petersburg, Russian Federation.
E MussoAO Ospedali Riuniti PO Vincenzo Cervello, Palermo, Italy.
L HavelThomayer Hospital, First Faculty of Medicine, Charles University, Prague, Czech Republic.
I BondarenkoDnipropetrovsk Medical Academy, Dnipro, Ukraine.
G LosonczySemmelweis University, Budapest, Hungary.
N ConevMedical Oncology, UMHAT St Marina, Varna, Bulgaria.
H MannAstraZeneca, Cambridge, UK.
T B DalviAstraZeneca, Gaithersburg USA.
H JiangAstraZeneca, Gaithersburg USA.
J W GoldmanDavid Geffen School of Medicine at UCLA, Los Angeles, USA.
AstraZeneca (United States) · USAsklepios Fachkliniken München-Gauting · DEAstraZeneca (United Kingdom) · GBBudgetary Health Care Institution of the Omsk Region "Clinical Oncology Center" · RUCharles University · CZDnipro State Medical University · UAHematology Oncology Consultants · USHospital Universitario 12 De Octubre · ESInstitute of Oncology NN Petrov · RUIstanbul University-Cerrahpaşa · TRKarl Landsteiner Society · ATKyiv City Clinical Oncology Center · UAOkayama University Hospital · JPOspedale Vincenzo Cervello · ITSamsung (South Korea) · KRSemmelweis University · HUUniversity 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

backgroundIn the phase III CASPIAN study, first-line durvalumab in combination with etoposide plus either cisplatin or carboplatin (EP) significantly improved overall survival (OS) versus EP alone in extensive-stage small-cell lung cancer (ES-SCLC). Durvalumab plus tremelimumab plus EP numerically improved OS versus EP, but did not reach statistical significance. Here we report updated OS in censored patients after median follow-up of >3 years. PATIENTS AND

methods805 patients with treatment-naïve ES-SCLC were randomized 1 : 1 : 1 to durvalumab plus EP, durvalumab plus tremelimumab plus EP, or EP. The two primary endpoints were OS for durvalumab plus EP versus EP and for durvalumab plus tremelimumab plus EP versus EP.

resultsAs of 22 March 2021 (median follow-up 39.4 months, 86% maturity), durvalumab plus EP continued to demonstrate improved OS versus EP: hazard ratio (HR) 0.71 [95% confidence interval (CI) 0.60-0.86; nominal P = 0.0003]; median OS was 12.9 versus 10.5 months, and 36-month OS rate was 17.6% versus 5.8%. Durvalumab plus tremelimumab plus EP continued to numerically improve OS versus EP: HR 0.81 (95% CI: 0.67-0.97; nominal P = 0.0200); median OS was 10.4 months, and 36-month OS rate was 15.3%. Twenty-seven and nineteen patients in the durvalumab plus EP and durvalumab plus tremelimumab plus EP arms, respectively, remained on durvalumab treatment at data cut-off.

conclusionsThree times more patients were estimated to be alive at 3 years when treated with durvalumab plus EP versus EP, with the majority still receiving durvalumab at data cut-off, further establishing durvalumab plus EP as first-line standard of care for ES-SCLC.

Indexed as

Lung NeoplasmsSmall Cell Lung CarcinomaAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsEtoposideHumansPlatinumAntibodies, MonoclonalAntibodies, Monoclonal, HumanizeddurvalumabEtoposidePlatinumtremelimumabCASPIANdurvalumabextensive-stage SCLCoverall survivaltremelimumab

Identifiers

PMID35279527
PMCPMC9161394
OpenAlexW4220970211

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.