The purpose of this registry is to collect data in order to discover whether melanoma patients with minimal SN tumor burden should undergo a complete lymph node dissection (CLND) or not. Currently, if a patient has a positive (or metastatic) SN, this patient will be offered a CLND, which is a surgical intervention aiming to remove all lymph nodes from the same nodal basin as the SN. However, if the positive (or metastatic) SN is only minimally involved, some centers and/or countries do not offer a CLND routinely. As a matter of fact, the CLND procedure does not increase survival for patients with a minimal SN tumor burden, but can add prognostic information, potentially useful in the subsequent decision-making process. However, this is a surgical operation for the patient, which might be accompanied by significant side effects. Moreover, only approximately 20% of patients with a metastatic SN have further lymph node metastases in the same basin, which means that about 4 patients out of 5 will not benefit from a CLND. Thus, there is an urgent need to identify which SN positive patients could be safely spared from a CLND. It has been demonstrated that breast cancer patients with minimal SN tumor burden can be safely managed with nodal observation only, without performing a CLND. There is evidence that the same situation exists in melanoma as well, but this needs to be validated and this is why we are conducting this registry. The results of this registry will be crucial to establish an accepted standard of care (CLND or nodal observation) for melanoma patients with minimal SN tumor burden.
Study Type
OBSERVATIONAL
Enrollment
296
U.Z. Leuven - Campus Gasthuisberg
Leuven, Belgium
CHRU de Lille
Lille, France
CHU de Nice - Hopital De L'Archet
Nice, France
Institut Gustave Roussy
Paris, France
Charite - Universitaetsmedizin Berlin - Campus Mitte
Berlin, Germany
Universitaetsklinikum - Essen
Essen, Germany
UniversitaetsMedizin Mannheim
Mannheim, Germany
Istituto Europeo di Oncologia
Milan, Italy
Istituto Nazionale Tumori IRCCS - Fondazione G. Pascale
Naples, Italy
Istituto Oncologico Veneto IRCCS - Ospedale Busonera
Padova, Italy
...and 12 more locations
Distant Metastasis Free Interval (DMFI)
Time frame: 5 years after last patient in
Regional Control Rate (secondary endpoint):
Time frame: 5 years after last patient in
Relapse Free Interval (RFI)
Time frame: 5 years after last patient in
Melanoma Specific Survival (MSS)
Time frame: 5 years after last patient in
Overall Survival (OS)
Time frame: 5 years after last patient in
Morbidity: rates of wound infections, lymphedema and neurological damage
Time frame: 5 years after last patient in
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