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Groningen International Study on Sentinel Nodes in Vulvar Cancer-III

RecruitingPhase 2

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

Who can join

Ages 18 and older · Women

Full eligibility criteria
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

About the study

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

What is being tested

Sponsor: University Medical Center Groningen · Participants: 157 · Started: Jan 1, 2021

Contact the study team

Official record on ClinicalTrials.gov — NCT05076942

Locations in the U.S.

CaliforniaUC Irvine Health/Chao Family Comprehensive Cancer Center, Orange
FloridaMount Sinai Medical Center, Miami Beach
MassachusettsBaystate Medical Center, Springfield
MichiganSpectrum Health at Butterworth Campus, Grand Rapids
Munson Medical Center, Traverse City
NebraskaNebraska Methodist Hospital, Omaha
NevadaWomen's Cancer Center of Nevada, Las Vegas
New JerseyMemorial Sloan Kettering Basking Ridge, Basking Ridge
Memorial Sloan Kettering Monmouth, Middletown
Memorial Sloan Kettering Bergen, Montvale
New YorkMemorial Sloan Kettering Commack, Commack
Memorial Sloan Kettering Westchester, Harrison
Memorial Sloan Kettering Cancer Center, New York
Memorial Sloan Kettering Nassau, Uniondale
North CarolinaDuke University Medical Center, Durham
Duke Women's Cancer Care Raleigh, Raleigh
OhioOhio State University Comprehensive Cancer Center, Columbus
ProMedica Flower Hospital, Sylvania
OklahomaUniversity of Oklahoma Health Sciences Center, Oklahoma City
Rhode IslandWomen and Infants Hospital, Providence
South DakotaAvera Cancer Institute, Sioux Falls

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.