Evidence map›Paper›PMID 38691813›Full record

ArticleJCO precision oncology2024

Natural History and Genomic Landscape of Chemotherapy-Resistant Muscle-Invasive Bladder Cancer.

Andrew T Lenis, Karissa Whiting, Vignesh Ravichandran, Jacob E Tallman, Syed M Alam, Carissa E Chu, Manual De Jesus Escano, Emily Bochner, Andrew Katims, Peter A Reisz and 24 more

Open access · greenAbstract read
In one paragraph

Article in JCO precision oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Article
  3. The promising arsenal of ferroptosis inducers in bladder cancer.Journal of molecular medicine (Berlin, Germany) · 2025
    Review
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

34 authors at 3 institutions in 1 country.

Andrew T LenisUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0001-9413-7793
Karissa WhitingBiostatistics Service, Department of Epidemiology & Biostatistics, MSK, New York, NY.ORCID 0000-0002-4683-1868
Vignesh RavichandranMarie-Josée and Henry R. Kravis Center for Molecular Oncology, MSK, New York, NY.ORCID 0000-0002-1532-2593
Jacob E TallmanUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0002-9930-6493
Syed M AlamUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0001-7854-2967
Carissa E ChuUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0003-3065-389X
Manual De Jesus EscanoUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0001-6347-4148
Emily BochnerUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0002-3008-0262
Andrew KatimsUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.
Peter A ReiszUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0002-1483-8133
Hong TruongUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0002-0225-0148
Timothy N ClintonUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.
Leon TelisUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.
Shawn DasonUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.
Victor McPhersonUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0003-4570-758X
Min Yuen TeoGenitourinary Oncology Service, Department of Medicine, MSK, New York, NY.ORCID 0000-0003-2511-6731
Samuel FuntGenitourinary Oncology Service, Department of Medicine, MSK, New York, NY.ORCID 0000-0002-7235-6319
David AggenGenitourinary Oncology Service, Department of Medicine, MSK, New York, NY.ORCID 0000-0003-3963-5751
Alvin C GohUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.
Timothy F DonahueUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0003-1855-1794
Eugene K ChaUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0002-8807-2353
S Machele DonatUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.
Harry W HerrUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.
Guido DalbagniUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.
Nikolaus SchultzMarie-Josée and Henry R. Kravis Center for Molecular Oncology, MSK, New York, NY.ORCID 0000-0002-0131-4904
Michael F BergerMarie-Josée and Henry R. Kravis Center for Molecular Oncology, MSK, New York, NY.ORCID 0000-0003-3882-5000
Dean F BajorinGenitourinary Oncology Service, Department of Medicine, MSK, New York, NY.ORCID 0000-0003-4001-7088
Jonathan E RosenbergGenitourinary Oncology Service, Department of Medicine, MSK, New York, NY.ORCID 0000-0003-2637-4249
Bernard H BochnerUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.ORCID 0000-0003-0846-0848
Irina OstrovnayaBiostatistics Service, Department of Epidemiology & Biostatistics, MSK, New York, NY.
Hikmat Al-AhmadieGenitourinary and Surgical Services, Department of Pathology, MSK, New York, NY.ORCID 0000-0002-2938-6627
David B SolitMarie-Josée and Henry R. Kravis Center for Molecular Oncology, MSK, New York, NY.ORCID 0000-0002-6614-802X
Gopa IyerGenitourinary Oncology Service, Department of Medicine, MSK, New York, NY.ORCID 0000-0002-5093-6099
Eugene J PietzakUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center (MSK), New York, NY.
Memorial Sloan Kettering Cancer Center · USNew York Oncology Hematology · USMolecular Oncology (United States) · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Michael Jason de la Cruz · 1985 to 2026
$347.4M
SPORE in Bladder CancerP50CA221745 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI OSTROVNAYA, IRINA · 2018 to 2024
$11.8M
MSK Paul Calabresi Career Development Award for Clinical OncologyK12CA184746 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Omar Abdel-Wahab, Simon N. Powell · 2015 to 2026
$8.3M
UROLOGY ONCOLOGY RESEARCH TRAINING GRANTT32CA082088 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Brett Stewart Carver · 1999 to 2026
$7.1M
Defining Mechanisms of Progression and Treatment Resistance in Localized Bladder CancerR37CA276946 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Eugene Pietzak · 2023 to 2026
$2.0M
NCI NIH HHS K12 CA184746NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA221745NCI NIH HHS R37 CA276946NCI NIH HHS T32 CA082088
6 · The paper itself

Abstract

purposePatients with residual invasive bladder cancer after neoadjuvant chemotherapy (NAC) and radical cystectomy have a poor prognosis. Data on adjuvant therapy for these patients are conflicting. We sought to evaluate the natural history and genomic landscape of chemotherapy-resistant bladder cancer to inform patient management and clinical trials.

methodsData were collected on patients with clinically localized muscle-invasive urothelial bladder cancer treated with NAC and cystectomy at our institution between May 15, 2001, and August 15, 2019, and completed four cycles of gemcitabine and cisplatin NAC, excluding those treated with adjuvant therapies. Survival was estimated using the Kaplan-Meier method, and multivariable Cox proportional hazards models were used to identify predictors of recurrence-free survival (RFS). Genomic alterations were identified in targeted exome sequencing (Memorial Sloan Kettering Integrated Mutation Profiling of Actionable Cancer Targets) data from post-NAC specimens from a subset of patients.

resultsLymphovascular invasion (LVI) was the strongest predictor of RFS (hazard ratio, 2.15 [95% CI, 1.37 to 3.39]) on multivariable analysis. Patients with ypT2N0 disease without LVI had a significantly prolonged RFS compared with those with LVI (70% RFS at 5 years). Lymph node yield did not affect RFS. Among patients with sequencing data (n = 101), chemotherapy-resistant tumors had fewer alterations in DNA damage response genes compared with tumors from a publicly available chemotherapy-naïve cohort (15%

conclusionAlthough chemotherapy-resistant bladder cancer generally portends a poor prognosis, patients with organ-confined disease without LVI may be candidates for close observation without adjuvant therapy. The genomic landscape of chemotherapy-resistant tumors is similar to chemotherapy-naïve tumors. Therapeutic opportunities exist for targeted therapies as adjuvant treatment in chemotherapy-resistant disease.

Indexed as

Drug Resistance, NeoplasmUrinary Bladder NeoplasmsAgedCisplatinCystectomyDeoxycytidineFemaleGemcitabineGenomicsHumansMaleMiddle AgedNeoadjuvant TherapyNeoplasm InvasivenessCisplatinDeoxycytidineGemcitabine

Identifiers

PMID38691813
PMCPMC11310921
OpenAlexW4396569275

What Socratic 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 Socratic graph.