Groningen International Study on Sentinel Nodes in Vulvar Cancer-III

NCT05076942RecruitingPHASE2INTERVENTIONAL

Summary

Key Facts

Lead Sponsor

University Medical Center Groningen

Enrollment

157

Start Date

2021-01-01

Completion Date

2028-01-01

Study Type

INTERVENTIONAL

Official Title

Groningen International Study on Sentinel Nodes in Vulvar Cancer-III, a Prospective Phase II Treatment Trial

Interventions

Radiotherapy combined with cisplatinCisplatin

Conditions

Vulvar CancerSentinel Lymph NodeLymph Node Metastases

Eligibility

Age Range

18 Years+

Sex

FEMALE

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 extracapsular extension, or
* Metastatic sentinel lymph node: more than 1 SN with metastasis ≤ 2mm
* Patients are able to understand requirements of study, provide written informed consent 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 alanine transaminase (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 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 fine needle 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 weeks before enrollment
* Pregnant female or nursing mother
* Desire to become pregnant
* Known brain or spinal cord metastases unless adequately treated (surgery or radiotherapy) with no evidence of progression and neurologically stable off anticonvulsants and steroids
* Unstable angina, myocardial infarction, cerebrovascular accident, \> Class II congestive heart failure according to the New York Heart Association Classification for Congestive Heart Failure (see Appendix B) within 6 months before enrollment

Outcome Measures

Primary Outcomes

Groin recurrence rate

Groin recurrence in the groin with SN metastasis treated with chemoradiation

Time frame: Within first 2 years after primary treatment

Secondary Outcomes

Treatment related morbidity

Short and longterm morbidty

Time frame: First two years after primary treatment

Quality of life as assessed using EORTC-QLQc30

Quality of life

Time frame: First two year after primary treatment

Quality of life-vulvar cancer specific, as assessed using VU34

Quality of life-vulvar cancer specific

Time frame: First two year after primary treatment

Locations

UC Irvine Health/Chao Family Comprehensive Cancer Center, Orange, United States

Mount Sinai Medical Center, Miami Beach, United States

Baystate Medical Center, Springfield, United States

Spectrum Health at Butterworth Campus, Grand Rapids, United States

Munson Medical Center, Traverse City, United States

Nebraska Methodist Hospital, Omaha, United States

Women's Cancer Center of Nevada, Las Vegas, United States

Memorial Sloan Kettering Basking Ridge, Basking Ridge, United States

Memorial Sloan Kettering Monmouth, Middletown, United States

Memorial Sloan Kettering Bergen, Montvale, United States

Memorial Sloan Kettering Commack, Commack, United States

Memorial Sloan Kettering Westchester, Harrison, United States

Memorial Sloan Kettering Cancer Center, New York, United States

Memorial Sloan Kettering Nassau, Uniondale, United States

Duke University Medical Center, Durham, United States

Duke Women's Cancer Care Raleigh, Raleigh, United States

Ohio State University Comprehensive Cancer Center, Columbus, United States

ProMedica Flower Hospital, Sylvania, United States

University of Oklahoma Health Sciences Center, Oklahoma City, United States

Women and Infants Hospital, Providence, United States

Avera Cancer Institute, Sioux Falls, United States

Catharina Hospital Eindhoven, Eindhoven, Netherlands

University Medical Center Groningen, Groningen, Netherlands

Leiden University Medical Center, Leiden, Netherlands

Radboud University Medical Center, Nijmegen, Netherlands

Erasmus Medical Center, Rotterdam, Netherlands

University Medical Center Utrecht, Utrecht, Netherlands

Linked Papers

2023-04-03

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)

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 ( 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. 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. 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. 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 2 mm in the sentinel node and/or extracapsular extension, or more than one sentinel node with micrometastasis ≤2 mm. Groin recurrence rate in the first 2 years after primary treatment. 157 patients with macrometastases in their SLN. January 1, 2029. NCT05076942.

Linked Investigators

Groningen International Study on Sentinel Nodes in Vulvar Cancer-III