Merkel Cell Carcinoma
Conditions
Brief summary
Nodal micrometastases-free rate defined as the rate of patients without nodal micrometastases after 2 cycles of treatment, determined by sentinel lymph node biopsy
Detailed description
Recurrence-free survival (RFS) defined as time from randomization until date of to the date of the first of the following events: i. MCC progression or ii. MCC recurrence or iii. MCC-related death (DSS), Overall survival (OS), defined as time from randomization until date of death from any cause, Disease specific survival (DSS), defined as time from randomization until date of MCC-related death, Quality of life (QoL) using FACT-M questionnaire: (i) FCRI-SF questionnaire (ii) mFACT-M questionnaire, Descriptive comparison of neoadjuvant Cemiplimab with placebo treatment prior to sentinel lymph node biopsy regarding: nodal micrometastases-free rate, RFS, OS, DSS, QoL, Assessment of safety of the treatment as determined by the incidence, nature, causality, frequency, timing and severity of adverse events using NCI CTCAE 5, Descriptive comparison of safety between neoadjuvant Cemiplimab and placebo treatment prior to sentinel lymph node biopsy, Correlation of identified biomarker with clinical outcome, i.e., nodal metastases-free rate, RFS, OS
Interventions
Sponsors
Eligibility
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nodal micrometastases-free rate defined as the rate of patients without nodal micrometastases after 2 cycles of treatment, determined by sentinel lymph node biopsy | — |
Secondary
| Measure | Time frame |
|---|---|
| Recurrence-free survival (RFS) defined as time from randomization until date of to the date of the first of the following events: i. MCC progression or ii. MCC recurrence or iii. MCC-related death (DSS), Overall survival (OS), defined as time from randomization until date of death from any cause, Disease specific survival (DSS), defined as time from randomization until date of MCC-related death, Quality of life (QoL) using FACT-M questionnaire: (i) FCRI-SF questionnaire (ii) mFACT-M questionnaire, Descriptive comparison of neoadjuvant Cemiplimab with placebo treatment prior to sentinel lymph node biopsy regarding: nodal micrometastases-free rate, RFS, OS, DSS, QoL, Assessment of safety of the treatment as determined by the incidence, nature, causality, frequency, timing and severity of adverse events using NCI CTCAE 5, Descriptive comparison of safety between neoadjuvant Cemiplimab and placebo treatment prior to sentinel lymph node biopsy, Correlation of identified biomarker with clini | — |
Countries
Germany