The Multicentre Selective Lymphadenectomy Trial - 3

What this study is about

The goal of this clinical trial is to demonstrate that there is no difference (non-inferiorty) in the 2 year recurrence-free survival (RFS) between 2 different surgical approaches for clinical Stage III melanoma. Following 6 weeks of standard neaodjuvant immunotherapy, patients will undergo either selective index lymph node resection (ILN) (identified at baseline as the largest affected lymph node) or the standard of care therapeutic lymph node dissection (TLND). The secondary aims are to assess if patients who are managed without TLND will have a reduction in surgical complications (less wound problems \& lymphoedema), an improved quality of life, at a lower healthcare utilisation.

Who can join (things the study team will check)

✅ You may be able to join if…

• Male or female patients ≥ 18 years of age at the time of consent
• Written informed consent
• Cytologically or histologically confirmed, resectable pathological Stage IIIB, C or D (Any T, N1b, N2b, N2c, N3b, or N3c) cutaneous or unknown primary melanoma, with or without primary tumour in situ
• A minimum of one macroscopic lymph node, defined as:
  • A palpable node, confirmed by pathology
  • A non-palpable node, but enlarged per RECIST 1.1 criteria (≥ 15 mm in shortest diameter) and confirmed by pathology
  • An ultrasound or PET/CT scan positive lymph node of any size, confirmed by pathology.
• Up to 3 satellite (defined as any foci of clinically evident cutaneous and/or subcutaneous metastases occurring within 2 cm of but discontinuous from the primary melanoma) or in-transit metastases (defined as clinically evident cutaneous and/or subcutaneous metastases occurring >2 cm from the primary melanoma in the region between the primary and the regional lymph node basin) are permitted if they are completely resectable.
• Lymph node involvement in the groin (iliac, inguinal or both), axilla or neck only and may be unilateral or bilateral. Concurrent popliteal, epitrochlear or triangular intermuscular space (TIS) nodes permitted, as long as fully resectable.
• Tumour amenable to a newly obtained core biopsy of a lesion which has not been previously irradiated. Archival tissue from a past primary or nodal lesion (if applicable) or tissue taken for current diagnosis will also be collected if available.
• Systemic neoadjuvant immunotherapy is scheduled for administration with at least one PD-(L)-1 check point inhibitor (e.g. nivolumab, pembrolizumab, cemiplimab). The immunotherapy regimen may include other checkpoint inhibitors (e.g. ipilimumab, relatlimab, fianlimab). The patient should meet the fitness for treatment requirements as detailed in the relevant regulatory-approved Product Information or Summary of Product Characteristics.
• Neoadjuvant course of treatment to be no longer than 6 weeks (allows for a maximum of 3 cycles at weeks 0, 3 and 6).
• Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
• Anticipated life expectancy of > 5 years.

🚫 You may not be able to join if…

• Uveal or mucosal melanoma.
• Isolated satellite or in-transit metastases only (without any cytological or histological proven lymph node involvement).
• Involvement of any lymph node basin other than groin, axilla or neck. Concurrent popliteal, epitrochlear or triangular intermuscular space (TIS) nodes permitted, as long as fully resectable.
• Clinical or radiographic evidence of distant metastasis (any AJCC 8th ed M Stage).
• Previous history of lymph node surgery to the same nodal basin, that was more extensive than a sentinel lymph node biopsy (SLNB).
• Previous radiotherapy to the same nodal basin.
• Any contraindication to the administration of nivolumab, ipilimumab, pembrolizumab or relatlimab per regulatory-approved product information and / or medical oncologist.
• Prior anti-PD-1, CTLA-4, PDL-1 or LAG 3 antibody exposure, or an agent directed to another stimulatory or co-inhibitory T-cell receptor for any disease or any chemotherapy or experimental local or systemic drug treatment.
• A plan to administer targeted therapy or any non-checkpoint inhibitor immunotherapy, or any intralesional therapy for melanoma in the neoadjuvant setting.
• A plan to administer any experimental immunotherapy as part of a clinical trial in the neoadjuvant setting.
• Known additional malignancies (unless adequately treated) active within the previous 3 years, except for locally curable cancers that have been apparently cured. The following malignancies, if undergone successful definitive resection or curative treatment, are permitted:
  • Basal cell carcinoma of the skin
  • Squamous cell carcinoma of the skin
  • Carcinoma in situ (e.g. breast carcinoma, cervical cancer in situ, but excluding carcinoma in situ of the bladder) that have undergone potentially curative therapy
  • Prostatic intraepithelial neoplasia
  • In situ melanoma
  • Atypical melanocytic hyperplasia
  • Stage I melanoma
  • Other malignancies for which the patient has been disease free for 3 years, not requiring active anti-cancer therapy.
• An active autoimmune disease or a requirement for chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 14 days prior to the first dose of study treatment. The following are permitted:
  • Replacement therapy (e.g. thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc)
  • Inhaled or intranasal corticosteroids (with minimal systemic absorption) may be continued if patient is on a stable dose
  • Non-absorbed intra-articular steroid injections.
• Has had an allogenic tissue/solid organ transplant.
• Active Hepatitis B (defined as Hepatitis B surface antigen [HBsAg] reactive) or Hepatitis C virus (defined as HCV RNA [qualitative] is detected) infection. Note: no testing for Hepatitis B and Hepatitis C is required unless mandated by local health authority.
• Has a known history of Human Immunodeficiency Virus (HIV). Note: no testing for HIV is required unless mandated by local health authority.
• Pregnant or breastfeeding females.
• Concurrent medical or social conditions that may prevent the patient from attending assessments or procedures per schedule.

Where this trial is running

• Cedars-Sinai Medical Centre, Los Angeles, California, United States
• Calvary Mater Newcastle, Newcastle, New South Wales, Australia
• Melanoma Institute Australia, Wollstonecraft, New South Wales, Australia
• Fiona Stanley Hospital, Murdoch, Western Australia, Australia
• Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
• Sheba Medical centre, Ramat Gan, Tel Aviv, Israel
• San Maria della Misericordia Hospital, Perugia, Italy
• The Royal Marsden, London, United Kingdom

Who to contact

Alexander CJ van Akkooi · +612 9911 7200 · alexander.vanakkooi@melanoma.org.au

It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT07049276.