Evidence map›Paper›PMID 32665122›Full record

ReviewUrologic oncology2022

TIM-3 and TIGIT are possible immune checkpoint targets in patients with bladder cancer.

Kyrollis Attalla, Adam M Farkas, Harry Anastos, Francois Audenet, Matthew D Galsky, Nina Bhardwaj, John P Sfakianos

Abstract readReview
In one paragraph

Review in Urologic oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Single-cell analysis reveals potential therapeutic markers of peripheral blood mononuclear cells from bladder cancer patients.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Natural killer cells: a promising immunotherapy for cancer.Journal of translational medicine · 2022
    Review
  13. Article
  14. NK Cells in aFrontiers in immunology · 2021
    Review
  15. Article
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

7 authors.

Kyrollis AttallaDepartment of Urology; Icahn School of Medicine at Mount Sinai, New York, NY.
Adam M FarkasDepartment of Medicine, Division of Hematology Oncology, Icahn School of Medicine at Mount Sinai, Tisch Cancer Institute, New York, NY.
Harry AnastosDepartment of Urology; Icahn School of Medicine at Mount Sinai, New York, NY.
Francois AudenetDepartment of Urology; Icahn School of Medicine at Mount Sinai, New York, NY.
Matthew D GalskyDepartment of Medicine, Division of Hematology Oncology, Icahn School of Medicine at Mount Sinai, Tisch Cancer Institute, New York, NY.
Nina BhardwajDepartment of Medicine, Division of Hematology Oncology, Icahn School of Medicine at Mount Sinai, Tisch Cancer Institute, New York, NY.
John P SfakianosDepartment of Urology; Icahn School of Medicine at Mount Sinai, New York, NY. Electronic address: john.sfakianos@mountsinai.org.

Funding

Dissecting myeloid cell-mediated resistance to immune checkpoint blockade in bladder cancerR01CA249175 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BHARDWAJ, NINA, GALSKY, MATTHEW · 2020 to 2024
$3.5M
NK cell exhaustion in metastatic melanomaR01CA201189 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BHARDWAJ, NINA · 2016 to 2020
$2.1M
NCI NIH HHS R01 CA201189NCI NIH HHS R01 CA249175
6 · The paper itself

Abstract

The resurgence of immunotherapy as an effective anticancer strategy has been coupled with more mature understandings of the underlying immune pathways and the development of novel immune checkpoint targets. The clinical development of antibodies first directed against cytotoxic T-lymphocyte-associated antigen 4, and later against program death 1, achieved durable disease control in a subset of patients across a large number of tumor types. Previous work demonstrates that targeting the programmed death 1 pathway alone does not result in complete restoration of T cell function and in some cancers, targeting this axis does not restore T cell function at all, suggesting a need to identify other molecules and inhibitory pathways that are involved in T cell exhaustion. In a comprehensive immune profiling study of patients with bladder cancer, we demonstrate T-cell immunoglobulin domain and mucin domain-containing molecule and T cell immunoglobulin and immunoreceptor tyrosine-based inhibitory motif domain as possible targets as perhaps monotherapy or in combination with other immune checkpoint inhibitors.

Indexed as

Hepatitis A Virus Cellular Receptor 2Urinary Bladder NeoplasmsHumansImmunotherapyProgrammed Cell Death 1 ReceptorReceptors, ImmunologicHepatitis A Virus Cellular Receptor 2Programmed Cell Death 1 ReceptorReceptors, ImmunologicTIGIT protein, human

Identifiers

PMID32665122
PMCPMC7980780

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Registered trials

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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.