Evidence map›Paper›PMID 41337691›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2026

Gemcitabine Intravesical System Plus Cetrelimab or Cetrelimab Alone as Neoadjuvant Therapy in Muscle-Invasive Bladder Cancer: SunRISe-4 Primary Analysis and Biomarker Results.

Andrea Necchi, Félix Guerrero-Ramos, Paul L Crispen, Bernardo Herrera-Imbroda, Rohan Garje, Bernadett Szabados, Charles C Peyton, Benjamin Pradere, Ja Hyeon Ku, Neal Shore and 12 more

Registry-linked trialAbstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04919512 (A Phase 2, Open-Label, Multi-Center, Randomized Study of TAR-200 in Combination With Cetrelimab and Cetrelimab Alone in Participants With Muscle-Invasive Urothelial Carcinoma of the Bladder Who Are Scheduled for Radical Cystectomy and Are Ineligible for or Refusing Platinum-Based Neoadjuvant Chemotherapy), which is not on this map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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.

NCT04919512 phase2completednot on this map

A Phase 2, Open-Label, Multi-Center, Randomized Study of TAR-200 in Combination With Cetrelimab and Cetrelimab Alone in Participants With Muscle-Invasive Urothelial Carcinoma of the Bladder Who Are Scheduled for Radical Cystectomy and Are Ineligible for or Refusing Platinum-Based Neoadjuvant Chemotherapy

TypeinterventionalSponsorJanssen Research & Development, LLCRan2022 to 2026Enrolled163ConditionsUrinary Bladder NeoplasmsArmsTAR-200, Cetrelimab
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Balancing immunity with Tregs.Nature biotechnology · 2026
    Article
  6. Roundup.Indian journal of urology : IJU : journal of the Urological Society of India
    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

22 authors.

Andrea NecchiDepartment of Medical Oncology, IRCCS San Raffaele Hospital, Comprehensive Cancer Center, Milan, Italy.ORCID 0000-0002-3007-2756
Félix Guerrero-RamosDepartment of Urology, Hospital Universitario 12 de Octubre, Madrid, Spain.ORCID 0000-0002-0767-3465
Paul L CrispenDepartment of Urology, University of Florida, Gainesville, FL.
Bernardo Herrera-ImbrodaUrology Department, Hospital Universitario Virgen de la Victoria, IBIMA-Plataforma BIONAND, Málaga, Spain.
Rohan GarjeMiami Cancer Institute, Miami, FL.ORCID 0000-0002-7244-5602
Bernadett SzabadosBarts Experimental Cancer Medicine Centre, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0002-8786-0032
Charles C PeytonDepartment of Urology, University of Alabama at Birmingham, Birmingham, AL.ORCID 0009-0008-8778-9759
Benjamin PradereDepartment of Urology, UROSUD, La Croix Du Sud Hospital, Quint-Fonsegrives, France.ORCID 0000-0002-7768-8558
Ja Hyeon KuSeoul National University Hospital, Seoul, South Korea.
Neal ShoreSTART Carolina Research, Myrtle Beach, SC.ORCID 0000-0001-5767-0548
Martin BögemannDepartment of Urology, Münster University Hospital, Münster, Germany.ORCID 0000-0002-2569-4446
Mark A PrestonDepartment of Urologic Surgery, Brigham & Women's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.ORCID 0000-0003-1010-8464
Evanguelos XylinasDepartment of Urology, Bichat-Claude Bernard Hospital, Assistance Publique-Hôpitaux de Paris, Université de Paris Cité, Paris, France.
Cristina Sanchez de LlanoJohnson & Johnson, Madrid, Spain.
Cinty GongJohnson & Johnson, Raritan, NJ.ORCID 0000-0003-1158-0699
Mohamad HasanJohnson & Johnson, Spring House, PA.
Karen UrtishakJohnson & Johnson, Spring House, PA.
Sebastiano BattagliaJohnson & Johnson, Spring House, PA.
Hind StitouJohnson & Johnson, Issy-les-Moulineaux, France.
Sumeet BhanvadiaJohnson & Johnson, Spring House, PA.
Hussein SweitiJohnson & Johnson, Spring House, PA.ORCID 0000-0002-8983-6052
Sarah P PsutkaUniversity of Washington, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-4207-7490

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeStandard of care for muscle-invasive bladder cancer (MIBC) is radical cystectomy (RC) with neoadjuvant cisplatin-based chemotherapy (NAC). However, many patients are ineligible for or refuse cisplatin. SunRISe-4 (ClinicalTrials.gov identifier: NCT04919512) is an open-label, multicenter, parallel-cohort phase II study assessing neoadjuvant gemcitabine intravesical system (TAR-200/gem-iDRS) plus cetrelimab or cetrelimab monotherapy in patients with MIBC.

methodsAdults with Eastern Cooperative Oncology Group performance status 0-1, cT2-T4a N0M0, ineligible/refusing NAC, and planned for RC were randomly assigned 5:3, stratified by transurethral resection of bladder tumor completeness (residual tumor ≤3 cm permitted) and T stage, to receive TAR-200 plus cetrelimab (cohort 1) or cetrelimab monotherapy (cohort 2). The primary end point was pathologic complete response (pCR) at RC. Secondary end points included recurrence-free survival (RFS) and safety. Exploratory end points included pathologic overall response (pOR; ≤ypT1N0) and circulating tumor (ct) and urinary tumor (ut) DNA molecular residual disease (MRD). Side-by-side descriptive efficacy summary was planned.

resultsAt the May 9, 2025, data cutoff, 159 patients were treated; 88 in cohort 1 and 46 in cohort 2 underwent RC. pCR, pOR, and 1-year RFS rates were 38%, 53%, and 77% in cohort 1 and 28%, 44%, and 64% in cohort 2, respectively. pCR rates were consistent across subgroups. No new safety signals were observed. Across cohorts, utDNA- status before RC (week 12) and utDNA clearance correlated with pCR (

conclusionTAR-200 plus cetrelimab provided higher pCR, pOR, and 1-year RFS rates compared with cetrelimab monotherapy, supporting further investigation of the neoadjuvant combination in MIBC. utDNA and ctDNA MRD results support further investigation as biomarkers for residual local and nonlocal disease, respectively.

Identifiers

PMID41337691
PMCPMC12931865

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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 Socratic graph.