Evidence map›Paper›PMID 30385724›Full record

ArticleJCI insight2018

Sitravatinib potentiates immune checkpoint blockade in refractory cancer models.

Wenting Du, Huocong Huang, Noah Sorrelle, Rolf A Brekken

Abstract read
In one paragraph

Article in JCI insight, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
–field-weighted citation impact
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

73 citing papers in PubMed.

  1. Trial
  2. Trial
  3. MRTX-500 Phase 2 Trial: Sitravatinib With Nivolumab in Patients With Nonsquamous NSCLC Progressing On or After Checkpoint Inhibitor Therapy or Chemotherapy.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2023
    Trial
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  5. Trial
  6. Review
  7. Review
  8. Article
  9. Article
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  12. An overview of BAP1 biological functions and current therapeutics.Biochimica et biophysica acta. Reviews on cancer · 2025
    Review
  13. Article
  14. Navigating TAM receptor dynamics in tumour immunotherapy.Cancer immunology, immunotherapy : CII · 2025
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

13 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

4 authors.

Wenting DuDivision of Surgical Oncology, Department of Surgery, and Hamon Center for Therapeutic Oncology Research, and.
Huocong HuangDivision of Surgical Oncology, Department of Surgery, and Hamon Center for Therapeutic Oncology Research, and.
Noah SorrelleDivision of Surgical Oncology, Department of Surgery, and Hamon Center for Therapeutic Oncology Research, and.
Rolf A BrekkenDivision of Surgical Oncology, Department of Surgery, and Hamon Center for Therapeutic Oncology Research, and.

Funding

Transport Oncophysics CoreU54CA210181 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WANG, RONGFU · 2016 to 2020
$9.3M
Exploitation of RAS signaling to develop therapy and early detection strategies for PDAR01CA192381 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI BREKKEN, ROLF A, WILKIE, THOMAS M · 2015 to 2019
$2.2M
NCI NIH HHS R01 CA192381NCI NIH HHS U54 CA210181
6 · The paper itself

Abstract

Immune checkpoint blockade has achieved significant therapeutic success for a subset of cancer patients; however, a large portion of cancer patients do not respond. Unresponsive tumors are characterized as being immunologically "cold," indicating that these tumors lack tumor antigen-specific primed cytotoxic T cells. Sitravatinib is a spectrum-selective tyrosine kinase inhibitor targeting TAM (TYRO3, AXL, MerTK) and split tyrosine-kinase domain-containing receptors (VEGFR and PDGFR families and KIT) plus RET and MET, targets that contribute to the immunosuppressive tumor microenvironment. We report that sitravatinib has potent antitumor activity by targeting the tumor microenvironment, resulting in innate and adaptive immune cell changes that augment immune checkpoint blockade. These results suggest that sitravatinib has the potential to combat resistance to immune checkpoint blockade and expand the number of cancer patients that are responsive to immune therapy.

Indexed as

AnilidesAnimalsClinical Trials as TopicFemaleImmunotherapyInjections, SubcutaneousMacrophagesMiceMice, Inbred C57BLNeoplasmsProtein Kinase InhibitorsPyridinesTumor MicroenvironmentAnilidesProtein Kinase InhibitorsPyridinessitravatinibCancer immunotherapyDrug therapyMacrophagesOncologyTherapeutics

Identifiers

PMID30385724
PMCPMC6238734

What OpenQuestion holds

Textmetadata
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.