Evidence map›Paper›PMID 37442672›Full record

Trial reportEuropean urology oncology2024

Long-term Outcomes of Chemoradiation for Muscle-invasive Bladder Cancer in Noncystectomy Candidates. Final Results of NRG Oncology RTOG 0524-A Phase 1/2 Trial of Paclitaxel + Trastuzumab with Daily Radiation or Paclitaxel Alone with Daily Irradiation.

Douglas M Dahl, Theodore G Karrison, M Dror Michaelson, Huong T Pham, Chin-Lee Wu, Gregory P Swanson, William U Shipley, Jacqueline Vuky, R Jeffrey Lee, Anthony L Zietman and 8 more

Open access · greenAbstract readClinical Trial, Phase IIClinical Trial, Phase I
In one paragraph

Trial report in European urology oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. The Role of Natural Compounds in Bladder Urothelial Carcinoma Treatment.International journal of molecular sciences · 2026
    Review
  4. Recent Advances and Future Directions in Bladder Preservation Therapy for Muscle-Invasive Bladder Cancer.International journal of urology : official journal of the Japanese Urological Association · 2025
    Review
  5. Review
  6. 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

18 authors at 13 institutions in 2 countries.

Douglas M DahlMassachusetts General Hospital Cancer Center, Boston, MA, USA. Electronic address: ddahl@mgh.harvard.edu.
Theodore G KarrisonNRG Oncology Statistics and Data Management Center, Philadelphia, PA, USA; University of Chicago, Chicago, IL, USA.
M Dror MichaelsonMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Huong T PhamVirginia Mason Medical Center, Seattle, WA, USA.
Chin-Lee WuMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Gregory P SwansonScott and White Memorial Hospital, Temple, TX, USA.
William U ShipleyMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Jacqueline VukyOHSU Knight Cancer Institute, Accrual-Virginia Mason CCOP, Portland, OR, USA.
R Jeffrey LeeIntermountain Medical Center, Salt Lake City, UT, USA.
Anthony L ZietmanMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Luis SouhamiThe Research Institute of the McGill University Health Centre (MUHC), Montreal, QC, Canada.
Brian K ChangParkview Research Center, Fort Wayne, IN, USA.
Richard L DemingMercy Medical Center - Des Moines, Accrual-Penrose Cancer Center, Penrose-St. Francis Health Services, Des Moines, IA, USA.
John A EllertonNevada Cancer Research Foundation NCORP, Las Vegas, NV, USA.
Howard M SandlerCedars-Sinai Medical Center, Los Angeles, CA, USA.
Joseph P RodgersNRG Oncology Statistics and Data Management Center, Philadelphia, PA, USA.
Felix Y FengUCSF Medical Center-Mission Bay, San Francisco, CA, USA.
Jason A EfstathiouMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Massachusetts General Hospital · USCedars-Sinai Medical Center · USIntermountain Medical Center · USMcGill University Health Centre · CANevada Cancer Research Foundation · USNRG Oncology · USOHSU Knight Cancer InstituteParkview Health · USPenrose-St. Francis Health Services · USScott & White Memorial Hospital · USUniversity of California San Francisco Medical Center · USUniversity of Illinois Chicago · USVirginia Mason Medical Center · US

Funding

NRG Oncology Network Group Operations Center - GY9 BIQSFP Reports/BudgetsU10CA180868 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI NORMAN WOLMARK · 2014 to 2026
$206.8M
Statistics CoreU10CA180822 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI James J. Dignam, GREG YOTHERS · 2014 to 2026
$146.4M
NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180868
6 · The paper itself

Abstract

backgroundChemo-radiation is a well-established alternative to radical cystectomy in patients with muscle-invasive bladder cancer. Many patients due to age or medical comorbidity are unfit for either radical cystectomy, or standard cisplatin- or 5-fluorouracil-based chemoradiation, and do not receive appropriate treatment with curative intent. We treated patients with a less aggressive protocol employing seven weekly doses of paclitaxel and daily irradiation. In those whose tumors showed overexpression of her2/neu, seven weekly doses of trastuzumab were also administered.

objectiveTo report the long-term survival outcomes and toxicity results of the of NRG Oncology RTOG 0524 study. DESIGN, SETTING, AND

participantsSeventy patients were enrolled and 65 (median age: 76 yr) were deemed eligible. Patients were assigned to daily radiation and weekly paclitaxel + trastuzumab (group 1, 20 patients) or to daily radiation plus weekly paclitaxel (group 2, 45 patients) based on tumor her2/neu overexpression. Radiation was delivered in 1.8 Gy fractions to a total dose of 64.8 Gy. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: The primary endpoint was unresolved treatment-related toxicity. The secondary endpoints were complete response rate, protocol completion rate, and disease-free and overall survival. RESULTS AND LIMITATIONS: Protocol therapy was completed by 60% (group 1) and 76% (group 2); complete response rates at 12 wk were 62% in each group. Acute treatment-related adverse events (AEs) of grade ≥3 were observed in 80% in group 1 and 58% in group 2. There was one treatment-related grade 5 AE in group 1. Unresolved acute treatment-related toxicity was 35% in group 1 and 31% in group 2. The median follow-up was 2.3 yr in all patients and 7.2 yr in surviving patients. Overall survival at 5 yr was 25.0% in group 1 and 37.8% in group 2 (33.8% overall). At 5 yr, disease-free survival was 15.0% in group 1 and 31.1% in group 2.

conclusionsIn a cohort of patients with muscle-invasive bladder cancer who are not candidates for cystectomy or cisplatin chemotherapy, chemoradiation therapy offers a treatment with a significant response rate and 34% 5-yr overall survival. While there were many AEs in this medically fragile group, there were few grade 4 events and one grade 5 event attributable to therapy. PATIENT SUMMARY: Patients with invasive bladder cancer who cannot tolerate surgery were treated with radiation and systemic therapy without surgically removing their bladders. Most patients tolerated the treatment, were able to keep their bladders, and showed a significant treatment response rate.

Indexed as

PaclitaxelUrinary Bladder NeoplasmsAgedAntineoplastic Combined Chemotherapy ProtocolsCisplatinHumansMusclesTrastuzumabCisplatinPaclitaxelTrastuzumabBladder cancerChemotherapyRadiation therapyTargeted therapy

Identifiers

PMID37442672
PMCPMC10782593
OpenAlexW4383874542

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.