Evidence map›Paper›PMID 37561425›Full record

ArticleJAMA oncology2023

Immunotherapy in the Treatment of Localized Genitourinary Cancers.

Andrea Necchi, Bishoy M Faltas, Susan F Slovin, Joshua J Meeks, Sumanta K Pal, Lawrence H Schwartz, Richard S P Huang, Roger Li, Brandon Manley, Jad Chahoud and 2 more

Open access · greenAbstract read
In one paragraph

Article in JAMA oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Article
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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

12 authors at 8 institutions in 2 countries.

Andrea NecchiVita-Salute San Raffaele University; IRCCS San Raffaele Hospital, Milan, Italy.
Bishoy M FaltasEnglander Institute for Precision Medicine, Weill Cornell Medicine-NewYork Presbyterian Hospital. New York, New York.
Susan F SlovinGenitourinary Oncology Service, Department of Medicine, Sidney Kimmel Center for Prostate and Urologic Cancers, Memorial Sloan Kettering Cancer Center, New York, New York.
Joshua J MeeksDepartments of Pathology, Urology, Biochemistry and Molecular Genetics, Northwestern University School of Medicine, Chicago, Illinois.
Sumanta K PalDepartment of Medical Oncology & Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, California.
Lawrence H SchwartzDepartment of Radiology, Columbia University College of Physicians and Surgeons, New York, New York.
Richard S P HuangFoundation Medicine, Cambridge, Massachusetts.
Roger LiDepartment of Genitourinary Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida.
Brandon ManleyDepartment of Genitourinary Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida.
Jad ChahoudDepartment of Genitourinary Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida.
Jeffrey S RossFoundation Medicine, Cambridge, Massachusetts.
Philippe E SpiessDepartment of Genitourinary Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida.
Moffitt Cancer Center · USFoundation Medicine (United States)City of Hope · USCornell University · USMemorial Sloan Kettering Cancer Center · USNewYork–Presbyterian Hospital · USNorthwestern University · USVita-Salute San Raffaele University · IT

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
BLRD VA I01 BX003692BLRD VA I01 BX005599NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Importance: A true revolution in the management of advanced genitourinary cancers has occurred with the discovery and adoption of immunotherapy (IO). The therapeutic benefits of IO were recently observed not to be solely confined to patients with disseminated disease but also in select patients with localized and locally advanced genitourinary neoplasms. Observations: KEYNOTE-057 demonstrated the benefit of pembrolizumab monotherapy for treating high-risk nonmuscle invasive bladder cancer unresponsive to bacillus Calmette-Guérin (BCG), resulting in recent US Food and Drug Administration approval. Furthermore, a current phase 3 trial (Checkmate274) demonstrated a disease-free survival benefit with the administration of adjuvant nivolumab vs placebo in muscle-invasive urothelial carcinoma after radical cystectomy. In addition, the recent highly publicized phase 3 KEYNOTE 564 trial demonstrated a recurrence-free survival benefit of adjuvant pembrolizumab in patients with high-risk localized/locally advanced kidney cancer. Conclusions and Relevance: The adoption and integration of IO in the management of localized genitourinary cancers exhibiting aggressive phenotypes are becoming an emerging therapeutic paradigm. Clinical oncologists and scientists should become familiar with these trials and indications because they are likely to dramatically change our treatment strategies in the months and years to come.

Indexed as

Carcinoma, Transitional CellUrinary Bladder NeoplasmsHumansImmunotherapyNeoplasm InvasivenessNeoplasm Recurrence, LocalNivolumabProgression-Free SurvivalNivolumab

Identifiers

PMID37561425
PMCPMC11429659
OpenAlexW4385716608

What OpenQuestion holds

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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.