Groningen International Study on Sentinel Nodes in Vulvar Cancer-III

Last updated: July 27, 2023
Sponsor: University Medical Center Groningen
Overall Status: Active - Recruiting

Phase

2

Condition

Genitourinary Cancer

Pelvic Cancer

Vaginal Cancer

Treatment

Radiotherapy combined with cisplatin

Cisplatin

Clinical Study ID

NCT05076942
2016-00601
NRG-GY024
  • Ages > 18
  • Female

Study Summary

Vulvar cancer patients with SN-metastasis > 2mm will receive chemoradiation instead of an inguinofemoral lymphadenectomy.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Histological confirmed primary SCC of the vulva
  • T1 tumor, not encroaching urethra/vagina/anus
  • Depth of invasion > 1mm
  • Tumor diameter < 4cm
  • Unifocal tumor
  • No enlarged (>1.5cm) or suspicious inguinofemoral lymph nodes at imaging (CT/MRI/ultrasound)
  • Possibility to obtain informed consent
  • Metastatic sentinel lymph node; size of metastasis > 2mm and / or extracapsularextension, or
  • Metastatic sentinel lymph node: more than 1 SN with metastasis ≤ 2mm
  • Patients are able to understand requirements of study, provide written informedconsent and comply with the study and follow-up procedures
  • Adequate bone marrow, renal and liver function:
  • Absolute neutrophil count ≥ 1.5 x 109 /L
  • Platelet count ≥ 100 x 109 /L
  • Creatinine clearance ≥ 40 ml/min measured by the Cockroft Gault formula
  • Total bilirubin < 1.25 x ULN Aspartate transaminase (AST) and alaninetransaminase (ALT) ≤ 2.5 x ULN
  • Performance status of 0, 1 or 2 on the Eastern Cooperative Oncology Group (ECOG) Scale (Appendix A)
  • Age 18 years or older
  • Life expectancy of ≥ 12 weeks
  • Written informed consent

Exclusion

Exclusion Criteria:

  • Inoperable tumors and tumors > 4cm
  • Multifocal tumors
  • Tumors with other pathology than squamous cell carcinoma
  • Patients with enlarged / suspicious lymph nodes which are proven metastatic after fineneedle aspiration cytology
  • No other carcinomas, other than basal cell carcinomas, within last 5 years
  • History of pelvic radiotherapy
  • History of any infection requiring hospitalization or antibiotics within 2 weeksbefore enrollment
  • Pregnant female or nursing mother
  • Desire to become pregnant
  • Known brain or spinal cord metastases unless adequately treated (surgery orradiotherapy) with no evidence of progression and neurologically stable offanticonvulsants and steroids
  • Unstable angina, myocardial infarction, cerebrovascular accident, > Class IIcongestive heart failure according to the New York Heart Association Classificationfor Congestive Heart Failure (see Appendix B) within 6 months before enrollment

Study Design

Total Participants: 157
Treatment Group(s): 2
Primary Treatment: Radiotherapy combined with cisplatin
Phase: 2
Study Start date:
January 01, 2021
Estimated Completion Date:
January 01, 2029

Study Description

Rationale:

Standard treatment of early stage vulvar cancer is a wide local excision of the primary tumor combined with the sentinel node (SN) procedure for the groins. An inguinofemoral lymphadenectomy (IFL) is only indicated in case of a positive SN. An IFL is associated with major morbidity, e.g. wound healing problems, lymphoceles, lymphedema of the legs and recurrent infections. GROINSS-V II investigated whether radiotherapy would be a safe alternative for IFL in case of SN metastasis. The results for radiotherapy in the group with metastasis ≤ 2mm are promising. This study also showed that for metastasis > 2mm, only radiotherapy was not efficient. The efficacy of treatment can be increased by adding chemotherapy or giving a higher dose of radiotherapy. GROINSS-V III will investigate this regimen.

Objective:

The primary objective of this study is to investigate the safety of replacing inguinofemoral lymphadenectomy by chemoradiation in early stage vulvar cancer patients with a macrometastasis (>2mm) and/or extracapsular extension in the SN. The secondary objective is to evaluate the short and long-term morbidity associated with the SN procedure and chemoradiation.

Study design: Phase II treatment trial, with stopping rules for the incidence of groin recurrences.

Study population: early-stage vulvar cancer patients with a metastasis > 2mm in their SN, or more than one metastasis ≤ 2mm.

Intervention: Participants will be treated with chemoradiation, in a total dose of 56Gy to the involved site, combined with weekly cisplatin 40mg/m2

Main study parameters/endpoints: The primary endpoint is the groin recurrence rate in the first 2 years after primary treatment.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: participants will be treated with chemoradiation during 5 weeks instead of surgical treatment. There is a risk that this treatment will not be as effective as surgical treatment, which may lead to more groin recurrences which are hard to treat. By continuously monitoring the groin recurrence rate the investigators will notice activation of the stopping rule as early as possible.

Connect with a study center

  • Catharina Hospital Eindhoven

    Eindhoven, 5623EJ
    Netherlands

    Active - Recruiting

  • University Medical Center Groningen

    Groningen, 9712RB
    Netherlands

    Active - Recruiting

  • Leiden University Medical Center

    Leiden, 2333ZA
    Netherlands

    Active - Recruiting

  • Radboud University Medical Center

    Nijmegen, 6525GA
    Netherlands

    Active - Recruiting

  • Erasmus Medical Center

    Rotterdam, 3015GD
    Netherlands

    Active - Recruiting

  • University Medical Center Utrecht

    Utrecht, 3584CX
    Netherlands

    Active - Recruiting

  • UC Irvine Health/Chao Family Comprehensive Cancer Center

    Orange, California 92868
    United States

    Active - Recruiting

  • Mount Sinai Medical Center

    Miami Beach, Florida 33140
    United States

    Active - Recruiting

  • Baystate Medical Center

    Springfield, Massachusetts 01199
    United States

    Active - Recruiting

  • Spectrum Health at Butterworth Campus

    Grand Rapids, Michigan 49503
    United States

    Active - Recruiting

  • Munson Medical Center

    Traverse City, Michigan 49684
    United States

    Active - Recruiting

  • Nebraska Methodist Hospital

    Omaha, Nebraska 68114
    United States

    Active - Recruiting

  • Women's Cancer Center of Nevada

    Las Vegas, Nevada 89106
    United States

    Active - Recruiting

  • Memorial Sloan Kettering Basking Ridge

    Basking Ridge, New Jersey 07920
    United States

    Active - Recruiting

  • Memorial Sloan Kettering Monmouth

    Middletown, New Jersey 07748
    United States

    Active - Recruiting

  • Memorial Sloan Kettering Bergen

    Montvale, New Jersey 07645
    United States

    Active - Recruiting

  • Memorial Sloan Kettering Commack

    Commack, New York 11725
    United States

    Active - Recruiting

  • Memorial Sloan Kettering Westchester

    Harrison, New York 10604
    United States

    Active - Recruiting

  • Memorial Sloan Kettering Cancer Center

    New York, New York 10065
    United States

    Active - Recruiting

  • Memorial Sloan Kettering Nassau

    Uniondale, New York 11553
    United States

    Active - Recruiting

  • Duke University Medical Center

    Durham, North Carolina 27710
    United States

    Active - Recruiting

  • Duke Women's Cancer Care Raleigh

    Raleigh, North Carolina 27607
    United States

    Active - Recruiting

  • Ohio State University Comprehensive Cancer Center

    Columbus, Ohio 43210
    United States

    Active - Recruiting

  • ProMedica Flower Hospital

    Sylvania, Ohio 43560
    United States

    Active - Recruiting

  • University of Oklahoma Health Sciences Center

    Oklahoma City, Oklahoma 73104
    United States

    Active - Recruiting

  • Women and Infants Hospital

    Providence, Rhode Island 02905
    United States

    Active - Recruiting

  • Avera Cancer Institute

    Sioux Falls, South Dakota 57105
    United States

    Active - Recruiting

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