Evidence map›Paper›PMID 35719865›Full record

ArticleJTO clinical and research reports2022

Impact of Brain Metastases on Treatment Patterns and Outcomes With First-Line Durvalumab Plus Platinum-Etoposide in Extensive-Stage SCLC (CASPIAN): A Brief Report.

Yuanbin Chen, Luis Paz-Ares, Niels Reinmuth, Marina Chiara Garassino, Galina Statsenko, Maximilian J Hochmair, Mustafa Özgüroğlu, Francesco Verderame, Libor Havel, György Losonczy and 7 more

Open access · goldAbstract read
In one paragraph

Article in JTO clinical and research reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
3.8field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

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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

17 authors at 16 institutions in 13 countries.

Yuanbin ChenCancer and Hematology Centers of Western Michigan, Grand Rapids, Michigan.
Luis Paz-AresDepartment of Medical Oncology, Hospital Universitario 12 de Octubre, Madrid, Spain.
Niels ReinmuthDepartment of Thoracic Oncology, Asklepios Lung Clinic, Munich-Gauting, Germany.
Marina Chiara GarassinoFondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Nazionale dei Tumori, Milan, Italy.
Galina StatsenkoOmsk Regional Cancer Center, Omsk, Russia.
Maximilian J HochmairDepartment of Respiratory and Critical Care Medicine, Karl Landsteiner Institute of Lung Research and Pulmonary Oncology, Krankenhaus Nord, Vienna, Austria.
Mustafa ÖzgüroğluDivision of Medical Oncology, Department of Internal Medicine, Cerrahpaşa School of Medicine, Istanbul University-Cerrahpaşa, Istanbul, Turkey.
Francesco VerderameAzienda Ospedaliera (AO) Ospedali Riuniti Presidio Ospedaliero (PO) Vincenzo Cervello, Palermo, Italy.
Libor HavelDepartment of Pneumology, First Faculty of Medicine, Thomayer Hospital, Charles University, Prague, Czechia.
György LosonczyDepartment of Pulmonology, Semmelweis University, Budapest, Hungary.
Nikolay V ConevMedical Oncology, UMHAT St Marina, Varna, Bulgaria.
Katsuyuki HottaCenter for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.
Jun Ho JiDepartment of Internal Medicine, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, South Korea.
Stuart SpencerAstraZeneca, Cambridge, United Kingdom.
Tapashi DalviAstraZeneca, Gaithersburg, Maryland.
Haiyi JiangAstraZeneca, Gaithersburg, Maryland.
Jonathan W GoldmanDavid Geffen School of Medicine at University of California Los Angeles (UCLA), Los Angeles, California.
AstraZeneca (United States) · USAsklepios Fachkliniken München-Gauting · DEAstraZeneca (United Kingdom) · GBBudgetary Health Care Institution of the Omsk Region "Clinical Oncology Center" · RUCharles University · CZFondazione IRCCS Istituto Nazionale dei Tumori · ITHematology Oncology Consultants · USHospital Universitario 12 De Octubre · ESIstanbul University-Cerrahpaşa · TRKarl Landsteiner Society · ATOkayama University Hospital · JPOspedale Vincenzo Cervello · ITSamsung (South Korea) · KRSemmelweis University · HUUniversity Hospital St. Marina · BGUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: In the phase 3 study involving the use of durvalumab with or without tremelimumab in combination with platinum-based chemotherapy in untreated extensive-stage SCLC (CASPIAN study), first-line durvalumab plus platinum-etoposide (EP) significantly improved overall survival (OS) versus EP alone ( Methods: Patients (WHO performance status 0 or 1), including those with asymptomatic or treated-and-stable brain metastases, were randomized to four cycles of durvalumab plus EP followed by maintenance durvalumab until progression or up to six cycles of EP and optional prophylactic cranial irradiation. Prespecified analyses of OS and progression-free survival (PFS) in subgroups with or without brain metastases used unstratified-Cox proportional hazards models. The data cutoff was on January 27, 2020. Results: At baseline, 28 out of 268 patients (10.4%) in the durvalumab plus EP arm and 27 out of 269 patients (10.0%) in the EP arm had known brain metastases, of whom 3 of 28 (10.7%) and 4 of 27 (14.8%) had previous brain radiotherapy, respectively. Durvalumab plus EP (versus EP alone) prolonged OS (hazard ratio, 95% confidence interval) in patients with (0.79, 0.44-1.41) or without (0.76, 0.62-0.92) brain metastases, with similar PFS results (0.73, 0.42-1.29 and 0.80, 0.66-0.97, respectively). Among patients without brain metastases, similar proportions in each arm developed new brain lesions as part of their first progression (8.8% and 9.5%), although 8.3% in the EP arm received prophylactic cranial irradiation. Similar proportions in each arm received subsequent brain radiotherapy (20.5% and 21.2%), although more common in patients with than without baseline brain metastases (45.5% and 18.0%). Conclusions: The OS and PFS benefit with first-line durvalumab plus EP were maintained irrespective of the presence of brain metastases, further supporting its standard-of-care use.

Indexed as

Brain metastasesCASPIANCentral nervous systemExtensive-stage SCLCImmunotherapy

Identifiers

PMID35719865
PMCPMC9204731
OpenAlexW4224923710

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.