Safety and efficacy of pembrolizumab, radiation therapy, and surgery versus radiation therapy and surgery for stage III soft tissue sarcoma of the extremity (SU2C-SARC032): An open-label, randomised clinical trial Journal Article


Authors: Mowery, Y. M.; Ballman, K. V.; Hong, A. M.; Schuetze, S. M.; Wagner, A. J.; Monga, V.; Heise, R. S.; Attia, S.; Choy, E.; Burgess, M. A.; Bae, S.; Pryor, D. I.; Van Tine, B. A.; Tinoco, G.; Chmielowski, B.; Freeman, C.; Gronchi, A.; Meyer, C. F.; Dickson, M. A.; Hartner, L.; Davis, L. E.; Powers, B. C.; Moding, E. J.; Weinhold, K. J.; van de Rijn, M.; Brigman, B. E.; Riedel, R. F.; Kirsch, D. G.
Article Title: Safety and efficacy of pembrolizumab, radiation therapy, and surgery versus radiation therapy and surgery for stage III soft tissue sarcoma of the extremity (SU2C-SARC032): An open-label, randomised clinical trial
Abstract: Background: Approximately half of patients with localised, high-risk soft tissue sarcoma of the extremity develop metastases. We aimed to assess whether the addition of pembrolizumab to preoperative radiotherapy and surgery would improve disease-free survival. Methods: We completed an open-label, randomised clinical trial in patients with grade 2 or 3, stage III undifferentiated pleomorphic sarcoma or dedifferentiated or pleomorphic liposarcoma of the extremity and limb girdle. Patients were enrolled at 20 academic institutions in Australia, Canada, Italy, and the USA. Patients were randomly assigned to preoperative radiotherapy then surgery (control group) or preoperative pembrolizumab with radiotherapy (initiated 1–14 days after the first dose of pembrolizumab) then surgery and postoperative pembrolizumab (experimental group). Pembrolizumab (200 mg intravenously every 3 weeks) was administered as three neoadjuvant cycles (before, during, and after radiotherapy) and 14 or less adjuvant cycles. Primary endpoint was disease-free survival. This study is registered with ClincialTrials.gov (NCT03092323). Findings: Between Nov 18, 2017, and Nov 14, 2023, 143 participants were randomly assigned to treatment. A modified intention-to-treat analysis of 127 patients with median follow-up of 43 months showed that the experimental group (n=64) had significantly longer disease-free survival than the control group (n=63; log-rank one-sided p=0·035; hazard ratio [HR] 0·61; 90% CI 0·39–0·96). The 2-year disease-free survival increased by 15% with addition of pembrolizumab: 52% (90% CI 42–64) and 67% (90% CI 58–78) for the control and experimental groups, respectively. Disease-free survival was similarly improved with pembrolizumab for the intention-to-treat patient population (HR 0·61 [90% CI 0·39–0·95]). Grade 3 or higher adverse events occurred more frequently in the experimental group (56%) than the control group (31%). Interpretation: Addition of pembrolizumab to preoperative radiotherapy and surgery improves disease-free survival for patients with stage III undifferentiated pleomorphic sarcoma and pleomorphic or dedifferentiated liposarcoma of the extremity, which establishes a promising new treatment option for these patients. Funding: Stand Up to Cancer and Merck Sharp & Dohme. © 2024 Elsevier Ltd
Keywords: osteosarcoma; adolescent; adult; child; controlled study; treatment response; cancer surgery; major clinical study; drug efficacy; drug safety; bone metastasis; adjuvant therapy; cancer radiotherapy; radiation dose; follow up; sensitivity analysis; cell proliferation; quality control; cancer immunotherapy; melanoma; progression free survival; apoptosis; phase 2 clinical trial; tumor volume; randomized controlled trial; tumor regression; histology; sarcoma; soft tissue; fibrosarcoma; soft tissue sarcoma; external beam radiotherapy; cancer control; spindle cell sarcoma; synovial sarcoma; antigen presenting cell; liposarcoma; chemoradiotherapy; clinical outcome; preoperative radiotherapy; acute myeloid leukemia; cancer prognosis; human; male; female; article; pembrolizumab
Journal Title: Lancet
Volume: 404
Issue: 10467
ISSN: 0140-6736
Publisher: Elsevier Science, Inc.  
Date Published: 2024-11-23
Start Page: 2053
End Page: 2064
Language: English
DOI: 10.1016/s0140-6736(24)01812-9
PUBMED: 39547252
PROVIDER: scopus
PMCID: PMC11842127
DOI/URL:
Notes: Article -- Source: Scopus
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  1. Mark Andrew Dickson
    169 Dickson