Neoadjuvant PD-1 blockade in surgically resectable desmoplastic melanoma: cohort A of the phase 2 SWOG S1512 trial

The phase 2 SWOG S1512 trial ( NCT02775851 ) was designed to evaluate the response to pembrolizumab (anti-PD-1) in individuals with desmoplastic melanoma. Here we report the results of cohort A of the trial, evaluating the pathological complete response (pCR) rate of neoadjuvant PD-1 blockade in surgically resectable desmoplastic melanoma. Secondary endpoints included clinical response rate, overall survival and toxicities. Twenty-eight eligible individuals with resectable desmoplastic melanoma received intravenous pembrolizumab (200 mg) every 3 weeks three times, followed by excision. Tissue samples before treatment, at 3-5 weeks after treatment initiation and at the time of surgery were reviewed. The primary endpoint of pCR rate by local pathological review was 71% (95% confidence interval, 51-87%; P < 0.001), which met the prespecified endpoint. There were two (7%) grade 3 treatment-related adverse events. At three years of follow-up, four participants have died, none known to be from melanoma or adverse events. In conclusion, neoadjuvant pembrolizumab in individuals with resectable desmoplastic melanoma results in a high pCR rate with acceptable safety profile. Clinicaltrials.gov: NCT02775851 .

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Publication Details

Journal
Nature Cancer
Published
2026-01-29
DOI
https://doi.org/10.1038/s43018-025-01113-y
Citations
2
Primary Topic
Cutaneous Melanoma Detection and Management
Type
article
Field-Weighted Citation Impact
48.39
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article

Neoadjuvant PD-1 blockade in surgically resectable desmoplastic melanoma: cohort A of the phase 2 SWOG S1512 trial

John Hyngstrom, Ivan Perez Garcilazo, Agustin Vega-Crespo, K. Norman et al.
2 citations
Nature Cancer
Cutaneous Melanoma Detection and Management
48.39
article

Neoadjuvant PD-1 blockade in surgically resectable desmoplastic melanoma: cohort A of the phase 2 SWOG S1512 trial

John Hyngstrom, Ivan Perez Garcilazo, Agustin Vega-Crespo, K. Norman, Andrew Scott Brohl, Shay Bellasea, Joseph Markowitz, Kari Kendra, Carlo M. Contreras, Jia Ming Chen, Tawnya L. Bowles, Egmidio Medina, J.A. Plaza, Kenneth F. Grossmann, Ignacio Baselga-Carretero, Elad Sharon, Cynthia R. Gonzalez, Siwen Hu-Lieskovan, Michael C. Wu, Katie M. Campbell, Nikhil I. Khushalani, David A. Wada, William E. Carson, Zeynep Eroglu, Antoni Ribas, Vernon K. Sondak, James Moon, Nataly Naser Al Deen, Bartosz Chmielowski, Alexandra Ikeguchi, Gino K. In, Sapna P. Patel
article en
2 citations

Abstract

The phase 2 SWOG S1512 trial ( NCT02775851 ) was designed to evaluate the response to pembrolizumab (anti-PD-1) in individuals with desmoplastic melanoma. Here we report the results of cohort A of the trial, evaluating the pathological complete response (pCR) rate of neoadjuvant PD-1 blockade in surgically resectable desmoplastic melanoma. Secondary endpoints included clinical response rate, overall survival and toxicities. Twenty-eight eligible individuals with resectable desmoplastic melanoma received intravenous pembrolizumab (200 mg) every 3 weeks three times, followed by excision. Tissue samples before treatment, at 3-5 weeks after treatment initiation and at the time of surgery were reviewed. The primary endpoint of pCR rate by local pathological review was 71% (95% confidence interval, 51-87%; P < 0.001), which met the prespecified endpoint. There were two (7%) grade 3 treatment-related adverse events. At three years of follow-up, four participants have died, none known to be from melanoma or adverse events. In conclusion, neoadjuvant pembrolizumab in individuals with resectable desmoplastic melanoma results in a high pCR rate with acceptable safety profile. Clinicaltrials.gov: NCT02775851 .

Nature CancerVol. 7(2)
University of Southern California (US), The University of Texas MD Anderson Cancer Center (US), University of California, Los Angeles (US), University of Utah (US), Huntsman Cancer Institute (US), Providence Portland Medical Center (US), The Ohio State University Wexner Medical Center (US), Intermountain Medical Center (US), Jefferson Healthcare (US), Moffitt Cancer Center (US), Fred Hutch Cancer Center (US), Dana-Farber Cancer Institute (US), Cancer Research Center (US), Oklahoma State University Oklahoma City (US), University of Colorado Cancer Center (US), National Cancer Institute (US), Rush University (US), University of Oklahoma (US), University of Colorado Denver (US)
Good health and well-being
Openalex Percentile: Top 0%
Cutaneous Melanoma Detection and Management
48.39
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