Long-term outcomes following melanoma metastasectomy categorized by response to immune checkpoint inhibitor (ICI) therapy.
Abstract
9563 Background: Patients undergoing surgical resection of Stage III/IV melanoma after response to ICIs show favorable survival, particularly with pathologic complete response (pCR). However, long-term outcomes of such patients stratified by ICI response remain undescribed. As surgery is increasingly employed in both PD-1 sensitive and refractory settings (e.g. tumor-infiltrating lymphocytes (TIL) therapy), better-defined outcomes and a clearer understanding of surgery's role are much needed. Methods: Patients treated with ICI (2003-2023) followed by metastasectomy were identified from a prospectively maintained database. Pre-surgery ICI response was assessed radiographically, and patients were categorized as having either stable/responding disease (R), an isolated site of disease progression (IP), or multiple progressing sites of disease (MP) for which surgery was pursued due to acute symptoms or palliative intent. Clinicopathologic factors examined included response to ICI, resection to no evidence of disease (NED), and pCR. Kaplan-Meier analyses with log-rank tests were used to compare disease-specific survival (DSS) from surgery date. Cox proportional hazards models identified independent predictors of DSS. Results: Among 513 patients, 426 (83%) had stage IV and 87 (17%) had stage III disease at ICI initiation. Patients were categorized as either R (n=76), IP (n=227), or MP (n=210). Fifty-three percent of patients received subsequent systemic therapy including 20 TIL patients, 12 of whom were in the MP group. Median follow-up after surgery among survivors was 2.51 years (IQR 0.93, 6.72). Median DSS following surgery was 4.1 years (95% CI: 2.5, NR). Resection to NED at the first operation post-ICI (n = 202, 39%) was associated with improved 5-year DSS [81% (75%, 88%) vs. 26% (20%, 33%); p < 0.001], with similar findings in only Stage IV patients (n = 426) [75% (67%, 84%) vs. 24% (19%, 32%); p<0.001]. Patients who underwent resection for an R or IP tumor had a 5-yr DSS of 89% (80%, 98%) or 62% (55%, 70%), respectively, compared to 20% (14%, 28%) for MP lesions (p < 0.001). Independent predictors of DSS also included NED resection and pCR (Table 1). Conclusions: Disease control after metastasectomy following ICI is durable, especially in patients with responding, stable, or isolated progressing disease, in addition to those achieving resection to NED or pCR. Alternative therapeutic strategies should be considered for patients with MP tumors as DSS remains poor after surgery alone. Multivariate model of DSS. p-value HR [95% CI] NED Status <0.001 0.31 [0.20, 0.49] Pre-operative Neutrophil-Lymphocyte Ratio 0.014 1.02 [1.01, 1.04] Response to ICI (R, IP, MP) <0.001 1.31 [0.65, 2.65] (R v. IP) 2.75 [1.35, 5.63] (R v. MP) pCR Status <0.001 0.22 [0.08, 0.65] Surgery Site 0.074 1.33 [0.97,1.83] Time from ICI Initiation to Surgery 0.006 0.85 [0.76, 0.97] M Stage 0.003 2.01 [1.21, 3.34]
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (12)
Aravind Sreeram
Johns Hopkins University School of Medicine, Baltimore, MD
Sabrina Lin
Memorial Sloan Kettering Cancer Center, New York, NY
Katherine Panageas
3Memorial Sloan Kettering Cancer Center, New York, United States
Parisa Momtaz
Monica F. Chen
Memorial Sloan Kettering Cancer Center, New York, NY
Edmund Bartlett
Mary Susan Brady
Memorial Sloan Kettering Cancer Center, New York, NY
Michael A. Postow
From the Sandra and Edward Meyer Cancer Center (J.D.W.) and the Department of Medicine (J.D.W., M.A.P.), Weill Cornell Medicine, and Memorial Sloan Kettering Cancer Center (M.A.P.) — both in New York; Istituto Oncologico Veneto, IRCCS, Padua (V.C.-S.), European Institute of Oncology, IRCCS, Milan (P.Q.), Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori, IRCCS, Meldola (M.G.), University of Siena and the Center for Immuno-Oncology, University Hospital of Siena, Siena (M.M.), and Istituto Nazionale Tumori IRCCS Fondazione Pascale, Naples (P.A.A.) — all in Italy; Maria Sklodowska-Curie National Institute of Oncology, Warsaw, Poland (P.R.); Texas Oncology–Baylor Charles A. Sammons Cancer Center, Dallas (C.L.C.); University Hospital Essen, the German Cancer Consortium, the National Center for Tumor Diseases–West, the Research Alliance Ruhr, Research Center One Health, and University Duisburg-Essen — all in Essen, Germany (D.S.); the College of Medicine, Swansea University, Swansea (J.W.), Brist...
James William Smithy
Memorial Sloan Kettering Cancer Center, New York, NY
Charlotte Eielson Ariyan
Memorial Sloan Kettering Cancer Center, New York, NY
Alexander Noor Shoushtari
Memorial Sloan Kettering Cancer Center, New York, NY
Danielle M. Bello
Memorial Sloan Kettering Cancer Center, New York, NY