NeoAdjuvant, Spare-Adjuvant (NASA) in Stage IIIB-IV (M1a) Melanoma
Sponsor: UNC Lineberger Comprehensive Cancer Center
ClinicalTrials ID:NCT07740941
This study assesses neoadjuvant PD-1-based regimens in stage IIIB-IV melanoma patients. Participants, aged 18+ with resectable disease, receive either pembrolizumab or ipilimumab plus nivolumab. Eligibility requires informed consent, ECOG 0-2, and adequate organ function. The trial examines 2-year OS without adjuvant therapy, focusing on non-inferiority in survival outcomes.
Patient Parameters
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Program Overview
This study evaluates the impact of neoadjuvant Programmed cell death Protein 1 (PD-1)-based treatment regimens in patients with resectable stage IIIB-M1a cutaneous or unknown primary melanoma at high risk of relapse without adjuvant therapy after definitive lymphadenectomy and irrespective of pathologic response outcome on the 2-year overall survival (OS). It was hypothesized that neoadjuvant PD1 inhibitor-based treatment without adjuvant treatment does not significantly (non-inferior) impact OS in this study patient population. Patients will be randomized to either two infusions of pembrolizumab or one infusion of ipilimumab plus nivolumab followed by a single infusion of nivolumab. Patients will undergo follow-up and restaging scans to assess event-free survival at 12 months and OS at 24 months after the first neoadjuvant treatment infusion.
Eligibility Criteria
Inclusion Criteria
- Written informed consent will be obtained to participate in the study, and HIPAA authorization for the release of personal health information.
- Subject is willing and able to comply with study procedures based on the judgment of the investigator or protocol designee, including randomization.
- Age ≥ 18 years at the time of consent.
- ECOG Performance Status of 0-2.
- Histological confirmation of cutaneous melanoma or melanoma of unknown primary.
- AJCC stage IIIB/IVa resectable disease that is measurable by iRECIST criteria.
- Adequate hematologic, renal, hepatic, and heart function
Exclusion Criteria
- Prior treatment with PD-1 Programmed cell death Protein 1 (PD-1) and Cytotoxic T-lymphocyte Antigen 4 (CTLA-4).
- Has an active autoimmune disease that requires systemic treatment with the use of disease-modifying agents or immunosuppressive drugs. For corticosteroids, up to 10 mg of prednisone daily, or an equivalent dose, is permitted. Hormone replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.
- Any condition, including laboratory abnormalities, that, in the opinion of the investigator, places the subject at unacceptable risk if he/she were to participate in the study. This includes, but is not limited to, serious medical conditions or psychiatric illnesses that are likely to interfere with participation in this clinical study.
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| Lineberger Comprehensive Cancer Center | 27599 | Chapel Hill | North Carolina |
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