Evidence map›Paper›PMID 35442707›Full record

Trial reportScience translational medicine2022

A phase 1-2 trial of sitravatinib and nivolumab in clear cell renal cell carcinoma following progression on antiangiogenic therapy.

Pavlos Msaouel, Sangeeta Goswami, Peter F Thall, Xuemei Wang, Ying Yuan, Eric Jonasch, Jianjun Gao, Matthew T Campbell, Amishi Yogesh Shah, Paul Gettys Corn and 16 more

Open access · greenAbstract readClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in Science translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
9.7field-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

39 citing papers in PubMed, 66 citations in OpenAlex.

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  5. Generalized Pairwise Comparisons in Dose Optimization Oncology Trials: Beyond Safety to Multi-outcome Dose Selection.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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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

26 authors at 2 institutions in 1 country.

Pavlos MsaouelDepartment of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0001-6505-8308
Sangeeta GoswamiDepartment of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0001-9201-4503
Peter F ThallDepartment of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Xuemei WangDepartment of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0002-3516-0966
Ying YuanDepartment of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Eric JonaschDepartment of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0003-0943-2806
Jianjun GaoDepartment of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0001-6138-4472
Matthew T CampbellDepartment of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0003-1915-4491
Amishi Yogesh ShahDepartment of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0002-9007-0621
Paul Gettys CornDepartment of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0002-4106-6335
Alda L TamDepartment of Interventional Radiology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0002-6065-1556
Kamran AhrarDepartment of Interventional Radiology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0002-7800-2300
Priya RaoDepartment of Pathology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0001-5672-0961
Kanishka SircarDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0001-9515-697X
Lorenzo CohenDepartment of Palliative, Rehabilitation and Integrative Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Sreyashi BasuThe Immunotherapy Platform, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0002-5028-3833
Fei DuanThe Immunotherapy Platform, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Sonali JindalThe Immunotherapy Platform, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0002-3911-6815
Yuwei ZhangThe Immunotherapy Platform, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Hong ChenThe Immunotherapy Platform, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0003-2315-0645
Shalini S YadavThe Immunotherapy Platform, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0001-8266-5548
Ronald ShazerMirati Therapeutics Inc., San Diego, CA 92121, USA.ORCID 0000-0002-0231-3436
Hirak Der-TorossianMirati Therapeutics Inc., San Diego, CA 92121, USA.ORCID 0000-0002-9902-5712
James P AllisonDepartment of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0001-8980-5697
Padmanee SharmaDepartment of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0003-4658-055X
Nizar M TannirDepartment of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0001-5559-8060
The University of Texas MD Anderson Cancer Center · USMirati Therapeutics (United States) · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

The accumulation of immune-suppressive myeloid cells is a critical determinant of resistance to anti-programmed death-1 (PD-1) therapy in advanced clear cell renal cell carcinoma (ccRCC). In preclinical models, the tyrosine kinase inhibitor sitravatinib enhanced responses to anti-PD-1 therapy by modulating immune-suppressive myeloid cells. We conducted a phase 1-2 trial to choose an optimal sitravatinib dose combined with a fixed dose of nivolumab in 42 immunotherapy-naïve patients with ccRCC refractory to prior antiangiogenic therapies. The combination demonstrated no unexpected toxicities and achieved an objective response rate of 35.7% and a median progression-free survival of 11.7 months, with 80.1% of patients alive after a median follow-up of 18.7 months. Baseline peripheral blood neutrophil-to-lymphocyte ratio correlated with response to sitravatinib and nivolumab. Patients with liver metastases showed durable responses comparable to patients without liver metastases. In addition, correlative studies demonstrated reduction of immune-suppressive myeloid cells in the periphery and tumor microenvironment following sitravatinib treatment. This study provides a rationally designed combinatorial strategy to improve outcomes of anti-PD-1 therapy in advanced ccRCC.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsLiver NeoplasmsAngiogenesis InhibitorsAnilidesFemaleHumansMaleNivolumabPyridinesTumor MicroenvironmentAngiogenesis InhibitorsAnilidesNivolumabPyridinessitravatinib

Identifiers

PMID35442707
PMCPMC11924199
OpenAlexW4224224667

What OpenQuestion holds

Textmetadata
LicenceTDM
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.