Radiotherapy combined with cisplatin: Inguinofemoral radiotherapy combined with weekly cisplatin
Cisplatin: Inguinofemoral radiotherapy combined with weekly cisplatin
Study summary
Vulvar cancer patients with SN-metastasis \> 2mm will receive chemoradiation instead of an inguinofemoral lymphadenectomy.
Eligibility
Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
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
Primary outcome measure(s)
Groin recurrence rate — Within first 2 years after primary treatment Groin recurrence in the groin with SN metastasis treated with chemoradiation
Trial sites (27)
Facility
City
Region
Status
UC Irvine Health/Chao Family Comprehensive Cancer Center
Orange
California
Recruiting
Mount Sinai Medical Center
Miami Beach
Florida
Recruiting
Baystate Medical Center
Springfield
Massachusetts
Recruiting
Spectrum Health at Butterworth Campus
Grand Rapids
Michigan
Recruiting
Munson Medical Center
Traverse City
Michigan
Recruiting
Nebraska Methodist Hospital
Omaha
Nebraska
Recruiting
Women's Cancer Center of Nevada
Las Vegas
Nevada
Recruiting
Memorial Sloan Kettering Basking Ridge
Basking Ridge
New Jersey
Recruiting
Memorial Sloan Kettering Monmouth
Middletown
New Jersey
Recruiting
Memorial Sloan Kettering Bergen
Montvale
New Jersey
Recruiting
Memorial Sloan Kettering Commack
Commack
New York
Recruiting
Memorial Sloan Kettering Westchester
Harrison
New York
Recruiting
Memorial Sloan Kettering Cancer Center
New York
New York
Recruiting
Memorial Sloan Kettering Nassau
Uniondale
New York
Recruiting
Duke University Medical Center
Durham
North Carolina
Recruiting
Duke Women's Cancer Care Raleigh
Raleigh
North Carolina
Recruiting
Ohio State University Comprehensive Cancer Center
Columbus
Ohio
Recruiting
ProMedica Flower Hospital
Sylvania
Ohio
Recruiting
University of Oklahoma Health Sciences Center
Oklahoma City
Oklahoma
Recruiting
Women and Infants Hospital
Providence
Rhode Island
Recruiting
Avera Cancer Institute
Sioux Falls
South Dakota
Recruiting
Catharina Hospital Eindhoven
Eindhoven
Netherlands
Recruiting
University Medical Center Groningen
Groningen
Netherlands
Recruiting
Leiden University Medical Center
Leiden
Netherlands
Recruiting
Radboud University Medical Center
Nijmegen
Netherlands
Recruiting
Erasmus Medical Center
Rotterdam
Netherlands
Recruiting
University Medical Center Utrecht
Utrecht
Netherlands
Recruiting
More University Medical Center Groningen trials in the Netherlands
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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