Evidence map›Paper›PMID 39499893›Full record

ArticleJCO precision oncology2024

DNA Damage Response Alterations Predict for Neoadjuvant Chemotherapy Sensitivity in Muscle-Invasive Bladder Cancer: A Correlative Analysis of the SWOG S1314 Trial.

Gopa Iyer, Catherine M Tangen, Michal Sarfaty, Ashley M Regazzi, I-Ling Lee, Megan Fong, Woonyoung Choi, Colin P N Dinney, Thomas W Flaig, Ian M Thompson and 3 more

Abstract 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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Effect of co-occurring mutations inFrontiers in immunology · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. 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

13 authors.

Gopa IyerMemorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-5093-6099
Catherine M TangenFred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0001-8825-8660
Michal SarfatyRabin Medical Center, Petah Tikva, Israel.ORCID 0000-0002-9603-3207
Ashley M RegazziMemorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-6019-1852
I-Ling LeeUniversity of Texas MD Anderson Cancer Center, Houston, TX.
Megan FongJohns Hopkins School of Medicine, Baltimore, MD.
Woonyoung ChoiJohns Hopkins School of Medicine, Baltimore, MD.ORCID 0000-0003-1088-9539
Colin P N DinneyUniversity of Texas MD Anderson Cancer Center, Houston, TX.
Thomas W FlaigSchool of Medicine, University of Colorado, Aurora, CO.ORCID 0000-0001-6145-9040
Ian M ThompsonCHRISTUS Medical Center Hospital, UT Health Science Center, San Antonio, TX.
Seth P LernerBaylor College of Medicine, Houston, TX.ORCID 0000-0002-6379-2581
David J McConkeyJohns Hopkins School of Medicine, Baltimore, MD.ORCID 0000-0003-1971-0638
Jonathan E RosenbergMemorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-2637-4249

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
SWOG Network Group Operations Center of the NCTNU10CA180888 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PRIMO N. LARA · 2014 to 2026
$152.1M
SWOG Statistics & Data Management Center complex - extension supplement for GY06U10CA180819 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Michael L. LeBlanc · 2014 to 2026
$115.2M
NCI NIH HHS P30 CA008748NCI NIH HHS U10 CA180819NCI NIH HHS U10 CA180888
6 · The paper itself

Abstract

purposeAlterations in DNA damage response (DDR) genes, including

methodsPretreatment tumor specimens from 179 evaluable patients underwent next-generation sequencing (Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets assay). Associations were determined between any or only deleterious alterations within nine predefined DDR genes, or any alterations in

resultsDeleterious DDR alterations were detected in 41 (23%) of 179 patients. Of the 151 patients evaluable for pathologic response, patients with deleterious DDR alterations (n = 39) demonstrated a higher pathologic response rate than those without (odds ratio [OR], 3.24 [95% CI, 1.51 to 6.94];

conclusionDeleterious DDR alterations were associated with pathologic response following NAC in S1314. Functional validation of

Indexed as

DNA DamageNeoadjuvant TherapyUrinary Bladder NeoplasmsAdultAgedCisplatinFemaleHumansMaleMiddle AgedNeoplasm InvasivenessXeroderma Pigmentosum Group D ProteinCisplatinERCC2 protein, humanXeroderma Pigmentosum Group D Protein

Identifiers

PMID39499893
PMCPMC12088707

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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.