Evidence map›Paper›PMID 34940094›Full record

ArticleCurrent oncology (Toronto, Ont.)2021

Phase Ib Study of Atezolizumab Plus Interferon-α with or without Bevacizumab in Patients with Metastatic Renal Cell Carcinoma and Other Solid Tumors.

Christian U Blank, Deborah J Wong, Thai H Ho, Todd M Bauer, Carrie B Lee, Fabiola Bene-Tchaleu, Jing Zhu, Xiaosong Zhang, Edward Cha, Mario Sznol

Open access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Current oncology (Toronto, Ont.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
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

10 authors at 7 institutions in 3 countries.

Christian U BlankNetherlands Cancer Institute-Antoni van Leeuwenhoek, 1066 Amsterdam, The Netherlands.
Deborah J WongDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.
Thai H HoDivision of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ 85259, USA.ORCID 0000-0003-0023-2939
Todd M BauerSarah Cannon Research Institute/Tennessee Oncology, PLLC, Nashville, TN 37203, USA.
Carrie B LeeDivision of Hematology/Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Fabiola Bene-TchaleuHoffmann-La Roche Ltd., Mississauga, ON L5N 5M8, Canada.
Jing ZhuGenentech, Inc., South San Francisco, CA 94080, USA.
Xiaosong ZhangGenentech, Inc., South San Francisco, CA 94080, USA.
Edward ChaGenentech, Inc., South San Francisco, CA 94080, USA.
Mario SznolYale Cancer Center, Yale School of Medicine, New Haven, CT 06520, USA.
Mayo Clinic in Arizona · USRoche (Canada) · CASarah Cannon · USThe Netherlands Cancer Institute · NLUniversity of California, Los Angeles · USUniversity of North Carolina at Chapel Hill · USYale Cancer Center · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
F. Hoffmann-La Roche n/aNCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

This Phase Ib study combined programmed death-ligand 1 inhibitor, atezolizumab, with other immunomodulatory agents in locally advanced and metastatic solid tumors. Arms B-D evaluated atezolizumab plus interferon-α, with/without vascular endothelial growth factor inhibitor, bevacizumab, in renal cell carcinoma (RCC) and other solid tumors. Arm B predominantly recruited patients with previously treated RCC or melanoma to receive atezolizumab plus interferon α-2b. Arm C investigated atezolizumab plus polyethylene glycol (PEG)-interferon α-2a in previously treated RCC. Arm D evaluated atezolizumab plus PEG-interferon α-2a and bevacizumab. Primary objectives were safety and tolerability; secondary objectives included clinical activity. Combination therapy was well tolerated, with safety profiles consistent with known risks of individual agents. The most frequent treatment-related toxicities were fatigue, chills, and pyrexia. The objective response rate (ORR) in arm B was 20.0% overall and 17.8% in patients with previously treated checkpoint inhibitor-naive RCC (

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAntibodies, Monoclonal, HumanizedBevacizumabHumansInterferon-alphaVascular Endothelial Growth Factor AAntibodies, Monoclonal, HumanizedatezolizumabBevacizumabInterferon-alphaVascular Endothelial Growth Factor Aatezolizumabbevacizumabcheckpoint inhibitioninterferon alfarenal cell carcinoma

Identifiers

PMID34940094
PMCPMC8700717
OpenAlexW4200622882

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.