SALVO: Single-arm phase II study of ipilimumab and nivolumab as adjuvant therapy for resected mucosal melanoma.

Authors

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Robert R. McWilliams

Mayo Clinic, Rochester, MN

Robert R. McWilliams, Shernan Holtan, Gregory Russell Pond, Yousef Zakharia, Brendan D. Curti, Evidio Domingo Musibay, Anthony J. Olszanski, Lisa A. Kottschade, Ralph J. Hauke

Organizations

Mayo Clinic, Rochester, MN, Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN, McMaster University, Department of Oncology, Hamilton, ON, Canada, Georgia Regents University, Augusta, GA, Earle A. Chiles Research Institute at Robert W. Franz Cancer Center, Providence Cancer Institute, Portland, OR, Fox Chase Cancer Center, Philadelphia, PA, Nebraska Cancer Specialists, Omaha, NE

Research Funding

Pharmaceutical/Biotech Company
Bristol-Myers Squibb.

Background: Mucosal melanoma is a rare and, therefore, poorly studied malignancy. Patients with resected primary tumors have a median time to recurrence of 5.5 months. While no one adjuvant therapy is of proven benefit for patients, immunotherapy has shown activity in metastatic mucosal melanoma. Methods: We are performing a single arm, phase II clinical trial through the Midwest Melanoma Partnership/Hoosier Cancer Research Network (6 sites) for resected mucosal melanoma. The primary endpoint is recurrence free survival (RFS), and it will include 36 subjects. Patients must have had an R0 or R1 resection of a mucosal melanoma (sinonasal, anorectal, vulvar, or other), and register within 90 days of surgery. Adjuvant radiation is allowed prior to registration but not required. Therapy consists of ipilimumab (1 mg/kg) and nivolumab (3 mg/kg) IV q3w x 4, then 480 mg nivolumab x 1 year. Statistical power is calculated to be 85% to detect a change in RFS from 5.5 months to 9.5 months, with a one sided alpha of 0.05. Enrollment began Sept 2017, with current participation from 6 large volume centers in the United States, with 17 patients enrolled as of Sept 2019. Full accrual is anticipated to complete by year end 2020. Patients will be followed for RFS and OS. Translational studies will include mutational burden, c-kit, BRAF, NRAS status, and serum markers of immunity -- including soluble PD-L1 and Bim. Clinical trial information: NCT03241186

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Abstract Details

Meeting

2020 ASCO-SITC Clinical Immuno-Oncology Symposium

Session Type

Trials in Progress Poster Session

Session Title

Trials in Progress Poster Session B

Track

Breast and Gynecologic Cancers,Developmental Therapeutics,Genitourinary Cancer,Head and Neck Cancer,Lung Cancer,Melanoma/Skin Cancers,Gastrointestinal Cancer,Combination Studies,Implications for Patients and Society,Miscellaneous Cancers,Hematologic Malignancies

Sub Track

Immune Checkpoints and Stimulatory Receptors

Clinical Trial Registration Number

NCT03241186

Citation

J Clin Oncol 38, 2020 (suppl 5; abstr TPS65)

Abstract #

TPS65

Poster Bd #

D10

Abstract Disclosures