Evidence map›Paper›PMID 33678522›Full record

Trial reportEuropean urology2021

Efficacy and Safety of Atezolizumab Plus Bevacizumab Following Disease Progression on Atezolizumab or Sunitinib Monotherapy in Patients with Metastatic Renal Cell Carcinoma in IMmotion150: A Randomized Phase 2 Clinical Trial.

Thomas Powles, Michael B Atkins, Bernard Escudier, Robert J Motzer, Brian I Rini, Lawrence Fong, Richard W Joseph, Sumanta K Pal, Mario Sznol, John Hainsworth and 14 more

Open access · greenAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in European urology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 4 pooled it
4.0field-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

27 citing papers in PubMed, 4 syntheses or guidelines pooled it, 43 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 20 institutions in 5 countries.

Thomas PowlesBarts Cancer Institute, Queen Mary University of London, London, UK. Electronic address: Thomas.Powles@bartshealth.nhs.uk.
Michael B AtkinsGeorgetown Lombardi Comprehensive Cancer Center, Washington, DC, USA.
Bernard EscudierGustave Roussy, Villejuif, France.
Robert J MotzerMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Brian I RiniVanderbilt University Medical Center, Nashville, TN, USA.
Lawrence FongUniversity of California, San Francisco, School of Medicine, San Francisco, CA, USA.
Richard W JosephMayo Clinic Hospital, Jacksonville, FL, USA.
Sumanta K PalCity of Hope Comprehensive Cancer Center, Duarte, CA, USA.
Mario SznolYale School of Medicine, New Haven, CT, USA.
John HainsworthSarah Cannon Research Institute, Nashville, TN, USA.
Walter M StadlerThe University of Chicago Medicine, Chicago, IL, USA.
Thomas E HutsonTexas Oncology-Baylor Charles A. Sammons Cancer Center, Dallas, TX, USA.
Alain RavaudCHU Hopitaux de Bordeaux, Hôpital Saint-André, Bordeaux, France.
Sergio BracardaAzienda Ospedaliera S. Maria, Terni, Italy.
Cristina SuarezVall d'Hebron Institute of Oncology, Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Barcelona, Spain.
Toni K ChoueiriDana-Farber Cancer Institute, Boston, MA, USA.
James ReevesFlorida Cancer Specialists & Research Institute, Fort Myers, FL, USA.
Allen CohnRocky Mountain Cancer Center, Denver, CO, USA.
Beiying DingGenentech, Inc., South San Francisco, CA, USA.
Ning LengGenentech, Inc., South San Francisco, CA, USA.
Kenji HashimotoRoche Products Ltd, Welwyn Garden City, UK.
Mahrukh HuseniGenentech, Inc., South San Francisco, CA, USA.
Christina SchiffGenentech, Inc., South San Francisco, CA, USA.
David F McDermottBeth Israel Deaconess Medical Center, Boston, MA, USA.
Azienda Ospedaliera S.Maria · ITBeth Israel Deaconess Medical Center · USCity of Hope · USDana-Farber Cancer Institute · USFlorida Cancer Specialists & Research Institute · USGeorgetown Lombardi Comprehensive Cancer CenterHôpital Saint-André · FRInstitut Gustave Roussy · FRMayo Clinic Hospital · USMemorial Sloan Kettering Cancer Center · USQueen Mary University of London · GBRoche (United Kingdom) · GBRocky Mountain Cancer Centers · USSarah Cannon · USTexas Oncology · USUniversitat Autònoma de Barcelona · ESUniversity of California, San Francisco · USUniversity of Chicago · USVanderbilt University Medical Center · USYale University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
Treating the P13-Kinase/AKTP50CA101942 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Wanling Xie · 2003 to 2026
$53.4M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA014599NCI NIH HHS P50 CA101942
6 · The paper itself

Abstract

backgroundThe use of immune checkpoint inhibitors combined with vascular endothelial growth factor (VEGF)-targeted therapy as second-line treatment for metastatic clear cell renal cancer (mRCC) has not been evaluated prospectively.

objectiveTo evaluate the efficacy and safety of atezolizumab + bevacizumab following disease progression on atezolizumab or sunitinib monotherapy in patients with mRCC. DESIGN, SETTING, AND

participantsIMmotion150 was a multicenter, randomized, open-label, phase 2 study of patients with untreated mRCC. Patients randomized to the atezolizumab or sunitinib arm who had investigator-assessed progression as per RECIST 1.1 could be treated with second-line atezolizumab + bevacizumab.

interventionPatients received atezolizumab 1200 mg intravenously (IV) plus bevacizumab 15 mg/kg IV every 3 wk following disease progression on either atezolizumab or sunitinib monotherapy. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: The secondary endpoints analyzed during the second-line part of IMmotion150 included objective response rate (ORR), progression-free survival (PFS), and safety. PFS was examined using Kaplan-Meier methods. RESULTS AND LIMITATIONS: Fifty-nine patients in the atezolizumab arm and 78 in the sunitinib arm were eligible, and 103 initiated second-line atezolizumab + bevacizumab (atezolizumab arm, n = 44; sunitinib arm, n = 59). ORR (95% confidence interval [CI]) was 27% (19-37%). The median PFS (95% CI) from the start of second line was 8.7 (5.6-13.7) mo. The median event follow-up duration was 19.4 (12.9-21.9) mo among the 25 patients without a PFS event. Eighty-six (83%) patients had treatment-related adverse events; 31 of 103 (30%) had grade 3/4 events. Limitations were the small sample size and selection for progressors.

conclusionsThe atezolizumab + bevacizumab combination had activity and was tolerable in patients with progression on atezolizumab or sunitinib. Further studies are needed to investigate sequencing strategies in mRCC. PATIENT SUMMARY: Patients with advanced kidney cancer whose disease had worsened during treatment with atezolizumab or sunitinib began second-line treatment with atezolizumab + bevacizumab. Tumors shrank in more than one-quarter of patients treated with this combination, and side effects were manageable.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsBevacizumabDisease ProgressionHumansSunitinibVascular Endothelial Growth Factor AAntibodies, Monoclonal, HumanizedatezolizumabBevacizumabSunitinibVascular Endothelial Growth Factor AAtezolizumabBevacizumabCancer immunotherapyMetastaticRenal cell carcinomaSecond lineSunitinibVascular endothelial growth factor inhibitor

Identifiers

PMID33678522
PMCPMC9357270
OpenAlexW3134509668

What OpenQuestion holds

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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.