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NCT01224665Completed

S1011 Standard or Extended Pelvic Lymphadenectomy in Treating Patients Undergoing Surgery for Invasive Bladder Cancer

A Phase III Surgical Trial to Evaluate the Benefit of a Standard Versus an Extended Pelvic Lymphadenectomy Performed at Time of Radical Cystectomy for Muscle Invasive Urothelial Cancer

Source: ClinicalTrials.gov · Last updated 29 Nov 2024

Brief summary (registry, in English)

RATIONALE: Lymphadenectomy may remove tumor cells that have spread to nearby lymph nodes in patients with invasive bladder cancer. It is not yet known whether extended pelvic lymphadenectomy is more effective than standard pelvic lymphadenectomy during surgery. PURPOSE: This randomized phase II trial is studying standard pelvic lymphadenectomy to see how well it works compared to extended pelvic lymphadenectomy in treating patients undergoing surgery for invasive bladder cancer.

Status (registry)
Completed
Study type
Interventional
Enrollment
658 (actual)
First submitted
19 Oct 2010
Start date
Nov 2011
Primary completion date
May 2024
Lead sponsor
SWOG Cancer Research Network
NCT number
NCT01224665

What you commit to

  • Study type: Interventional
  • Participants enrolled: 658
  • From Nov 2011 to the primary completion date, May 2024
  • 35 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • DISEASE CHARACTERISTICS:
  • Histologically confirmed urothelial carcinoma of the bladder
    • Stage T2, T3, or T4a disease
    • No clinical stage consistent with a low-risk of node metastasis (CIS only, T1)
    • No T4b disease (fixed lesion)
    • Disease that requires primary radical cystectomy and lymph node dissection for definitive treatment
    • No laparoscopic surgery
  • Predominant urothelial carcinoma with any of the following elements allowed:
    • Adenocarcinoma
    • Squamous cell carcinoma
    • Micropapillary or minor components of other rare phenotype
    • No pure squamous cell carcinoma or adenocarcinoma
  • No visceral or nodal metastatic disease proximal to the common iliac bifurcation by 2-view chest x-ray and abdominal-pelvic imaging by computerized tomography or MRI of the abdomen and pelvis
  • No intra-operative pelvic lymph node involvement (confirmed by frozen section) at or above the bifurcation of the common iliac vessels in any of the extended template
    • PATIENT CHARACTERISTICS:
  • Zubrod performance status 0-2
  • ALT and AST ≤ upper limit of normal (ULN)\*
  • Alkaline phosphatase ≤ ULN\*
  • Not pregnant or nursing
  • Fertile patients must use an effective contraception
  • No other prior malignancy except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or stage I or II cancer from which the patient is in complete remission for the past 5 years
  • Medically suitable to undergo cystectomy, in the physician's opinion NOTE: \*Levels may be ≥ ULN provided metastatic disease is excluded using dedicated liver imaging, bone scan, or biopsy.
    • PRIOR CONCURRENT THERAPY:
  • See Disease Characteristics
  • No prior partial cystectomy for invasive bladder cancer
  • No prior pelvic surgery that would obviate a complete extended lymphadenectomy (e.g., aorto-femoral/iliac bypass)
  • Prior neoadjuvant chemotherapy for this cancer allowed provided it has been completed and patient has recovered
  • No prior pelvic irradiation

Age in the registry: 18 years to 120 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (35)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
QEII Health Sciences Centre/Capital District Health Authority
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HalifaxCanadaUnknown status
London Regional Cancer Program
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LondonCanadaUnknown status
The Research Institute of the McGill University Health Centre (MUHC)
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MontrealCanadaUnknown status
McGill University Department of Oncology
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MontrealCanadaUnknown status
University Health Network, Princess Margaret Hospital
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TorontoCanadaUnknown status
BCCA - Vancouver Cancer Centre
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VancouverCanadaUnknown status
University of Colorado Cancer Center - Anschutz Cancer Pavilion
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AuroraUnited StatesUnknown status
Johns Hopkins University/Sidney Kimmel Cancer Center
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BaltimoreUnited StatesUnknown status
Brigham and Women's Hospital
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BostonUnited StatesUnknown status
University of Chicago Comprehensive Cancer Center
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ChicagoUnited StatesUnknown status
Cleveland Clinic Foundation
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ClevelandUnited StatesUnknown status
Ohio State University Comprehensive Cancer Center
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ColumbusUnited StatesUnknown status
UT Southwestern/Simmons Cancer Center-Dallas
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DallasUnited StatesUnknown status
Parkland Memorial Hospital
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DallasUnited StatesUnknown status
Baylor Saint Luke's Medical Center
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HoustonUnited StatesUnknown status
Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center
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HoustonUnited StatesUnknown status
M D Anderson Cancer Center
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HoustonUnited StatesUnknown status
USC / Norris Comprehensive Cancer Center
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Los AngelesUnited StatesUnknown status
Los Angeles County-USC Medical Center
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Los AngelesUnited StatesUnknown status
Loyola University Medical Center
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MaywoodUnited StatesUnknown status
Yale University
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New HavenUnited StatesUnknown status
Memorial Sloan-Kettering Cancer Center
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New YorkUnited StatesUnknown status
Stanford Cancer Institute
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Palo AltoUnited StatesUnknown status
Portland Veterans Administration Medical Center
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PortlandUnited StatesUnknown status
Oregon Health and Science University
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PortlandUnited StatesUnknown status
University of Rochester
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RochesterUnited StatesUnknown status
Mayo Clinic
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RochesterUnited StatesUnknown status
University of California Davis Comprehensive Cancer Center
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SacramentoUnited StatesUnknown status
Audie L Murphy Veterans Affairs Hospital
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San AntonioUnited StatesUnknown status
University of Texas Health Science Center at San Antonio
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San AntonioUnited StatesUnknown status
UCSF Medical Center-Mission Bay
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San FranciscoUnited StatesUnknown status
UCSF Medical Center-Mount Zion
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San FranciscoUnited StatesUnknown status
Louisiana State University Health Sciences Center Shreveport
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ShreveportUnited StatesUnknown status
Washington University School of Medicine
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St LouisUnited StatesUnknown status
Moffitt Cancer Center
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TampaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.