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  5. Long-Term Survival of Patients with Advanced/Metastatic Synovial Sarcoma or Myxoid/Round Cell Liposarcoma Who Received the T-Cell Receptor T-Cell Therapy, Afamitresgene Autoleucel, in the Phase 2 Spearhead-1 Trial

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Article
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2025

Long-Term Survival of Patients with Advanced/Metastatic Synovial Sarcoma or Myxoid/Round Cell Liposarcoma Who Received the T-Cell Receptor T-Cell Therapy, Afamitresgene Autoleucel, in the Phase 2 Spearhead-1 Trial

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en
2025
Vol 31 (2)
Vol. 31
DOI: 10.1016/j.jtct.2025.01.380

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Jean Yves Blay
Jean Yves Blay

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Sandra P. D’Angelo
Mihaela Druta
Brian A. Van Tine
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Abstract

Synovial sarcoma (SyS) and myxoid/round cell liposarcoma (MRCLS) are rare sarcoma subtypes, each representing 5–10% of soft tissue sarcomas , which typically express the intracellular cancer/testis antigen melanoma-associated antigen (MAGE) A4. Retrospective studies report median overall survival (OS) of 22.3 (95% CI: 19.7–24.1) months (mo) from metastasis diagnosis in SyS (Moreau-Bachelard C, ESMO Open 2022;7:100402), and of 16 (95% CI:13.5–18.9) mo and 26 (95% CI: 19.2–32.1) mo in SyS and MRCLS, respectively, from start of second-line therapy (Pollack SM, Cancer Med 2020;9:4593). Afamitresgene autoleucel (afami-cel) is a MAGE-A4–directed genetically modified autologous T-cell immunotherapy recently approved by the US Food and Drug Administration (FDA) for adults with unresectable/metastatic SyS who have received prior chemotherapy , are human leukocyte antigen (HLA)-A*02 eligible, and whose tumor expresses MAGE-A4 as determined by FDA-approved diagnostics. Afami-cel is infused into patients (pts) following lymphodepletion chemotherapy. Afami-cel met its primary efficacy endpoint in the Phase 2 open-label SPEARHEAD-1 trial (NCT04044768), in which 19/52 Cohort 1 pts with advanced/metastatic SyS or MRCLS had a response (D'Angelo SP, Lancet 2024;403:1460). Cytopenias were the most common Grade ≥3 adverse events . As of Aug 30, 2023, after a median follow-up time of 32.6 mo, median OS was 15.4 mo (95% CI: 10.9–28.7); follow-up is ongoing. Identify/characterize pts with advanced SyS or MRCLS who experienced long-term (∼3 year) survival post afami-cel and explore potential contributing factors. SPEARHEAD-1 was performed as described with 52 HLA-eligible pts with MAGE-A4–expressing advanced/metastatic SyS or MRCLS in Cohort 1. This survival analysis was ad hoc; formal statistical testing not performed. As of Jul 25, 2024, 13/52 (25%) Cohort 1 pts (12 with SyS, one with MRCLS) had OS >149 weeks (∼34 mo) after receiving afami-cel in Cohort 1 of SPEARHEAD-1. Baseline and treatment characteristics of the overall SPEARHEAD-1 Cohort 1 and of this subset of 13 long-term survivors are shown in the Table . Tumor expression of the target antigen, MAGE-A4, measured by immunohistochemistry , was slightly higher in this subset; previous lines of therapy and number receiving bridging therapy were slightly lower. Twelve of 13 had best overall response of partial response; one had stable disease. Cytokine release syndrome (CRS) occurred at similar levels in the overall cohort 1 of 52 pts (37 [71%] pts, with one Grade 3 event) and in the subset of 13 pts (nine [69%] pts, at Grade 1 in seven, Grade 2 in two). To date, survival of ∼3 years after treatment with afami-cel has been observed in 25% of pts with advanced/metastatic SyS or MRCLS in Cohort 1 of SPEARHEAD-1; work is ongoing to delineate potential mechanisms/factors influencing this.

How to cite this publication

Sandra P. D’Angelo, Mihaela Druta, Brian A. Van Tine, Scott M. Schuetze, Jean Yves Blay, Claudia Maria Valverde Morales, Édouard Forcade, Kristen N. Ganjoo, Axel Le Cesne, Sandra J. Strauss, Dejka M. Araujo, Edwin Choy, Christopher D. Dupont, Dennis Williams, Jane P. F. Bai, Lilliam Fernandes, Erin Van Winkle, Amber K. O’Connor, Elliot Norry (2025). Long-Term Survival of Patients with Advanced/Metastatic Synovial Sarcoma or Myxoid/Round Cell Liposarcoma Who Received the T-Cell Receptor T-Cell Therapy, Afamitresgene Autoleucel, in the Phase 2 Spearhead-1 Trial. , 31(2), DOI: https://doi.org/10.1016/j.jtct.2025.01.380.

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Publication Details

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Article

Year

2025

Authors

19

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0

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Language

en

DOI

https://doi.org/10.1016/j.jtct.2025.01.380

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