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Phase II activity trial of high-dose radiation and chemosensitization in patients with macrometastatic lymph node spread after sentinel node biopsy in vulvar cancer: GROningen INternational Study on Sentinel nodes in Vulvar cancer III (GROINSS-V III/NRG-GY024)
  1. Lilian T Gien1,
  2. Brian Slomovitz2,
  3. Ate Van der Zee3 and
  4. Maaike Oonk3
  1. 1Department of Gynecologic Oncology, Odette Cancer Centre, Toronto, Ontario, Canada
  2. 2Mount Sinai Medical Center, Miami Beach, Florida, USA
  3. 3Department of Gynecologic Oncology, University Medical Centre Groningen, Groningen, The Netherlands
  1. Correspondence to Dr Lilian T Gien, Department of Gynecologic Oncology, Odette Cancer Centre, Toronto, ON M4N 3M5, Canada; Lilian.Gien{at}sunnybrook.ca

Abstract

Background Standard treatment of early-stage vulvar cancer is a radical, wide, local excision of the primary tumor and a sentinel lymph node (SLN) procedure for the groins. An inguinofemoral lymphadenectomy is no longer necessary for patients who have a negative SLN or micrometastasis (2 mm). When there is macrometastasis (>2 mm) in the SLN, an inguinofemoral lymphadenectomy is indicated; however, this procedure is associated with major morbidity, such as wound healing, lymphoceles, and lymphedema.

Primary Objective To investigate the safety of replacing inguinofemoral lymphadenectomy by chemoradiation in patients with early-stage vulvar cancer with a macrometastasis (>2 mm) and/or extracapsular extension in the sentinel node.

Study Hypothesis Combination of 56 Gy of radiation to the inguinal site and concurrent cisplatin chemotherapy without completion inguinofemoral lymphadenectomy will be feasible and safe, with low groin recurrence rates.

Trial Design This is a single-arm, prospective phase II treatment trial with stopping rules for unacceptable groin recurrences. Eligible patients will receive 56 Gy of radiation to the involved inguinal site and chemotherapy with concurrent cisplatin.

Major Inclusion/Exclusion Criteria Eligible patients undergoing sentinel node procedure will have stage I, unifocal, invasive (>1 mm depth of invasion) squamous cell carcinoma of the vulva with tumor size <4 cm, and no suspicious nodes on imaging. Those eligible for the trial are those with a metastasis >2 mm in the sentinel node and/or extracapsular extension, or more than one sentinel node with micrometastasis ≤2 mm.

Primary Endpoint Groin recurrence rate in the first 2 years after primary treatment.

Sample Size 157 patients with macrometastases in their SLN.

Estimated Dates for Completing Accrual and Presenting Results January 1, 2029.

Trial Registration Number NCT05076942.

  • Vulvar Neoplasms
  • Sentinel Lymph Node
  • Gynecologic Surgical Procedures
  • Radiation Oncology

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Footnotes

  • Contributors MO is the global Principal Investigator of the GROINSS-V III clinical trial and the guarantor of this study. AVdZ is a Co-Investigator of the trial and the senior author on GROINSS-V and GROINSS-V II trials. BS is the NRG Oncology Principal Investigator of the GROINSS-V III trial. LTG is the NRG Oncology Co-Principal Investigator of this trial and primary author of this manuscript. All authors contributed to the content and editing of this manuscript.

  • Funding This study was funded by Universitair Medisch Centrum Groningen, KWF Kankerbestrijding, National Cancer Institute.

  • Competing interests None declared.

  • Provenance and peer review Commissioned; internally peer reviewed.