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Poster session 06

1729P - Update on SAINT: A phase II study using trabectedin (T) in combination with ipilimumab (I) and nivolumab (N) in previously treated soft tissue sarcoma

Date

14 Sep 2024

Session

Poster session 06

Topics

Tumour Site

Sarcoma

Presenters

Anmol Dia Agarwal

Citation

Annals of Oncology (2024) 35 (suppl_2): S1031-S1061. 10.1016/annonc/annonc1610

Authors

A.D. Agarwal1, S. Jeffrey1, R. Cechini1, V. Kumar1, N. Omelchenko1, J. ballon1, A. Moradkhani2, V.S. Chua Alcala3, N.S. Chawla4, S. Mahesh5, S.P. Chawla6, E.M. Gordon7

Author affiliations

  • 1 Research, Sarcoma Oncology Research Center, 90403 - Santa Monica/US
  • 2 Medical Oncology, SarcomaOncologyResearchCenter, 90403 - SantaMonica/US
  • 3 Clinical Research, Sarcoma Oncology Research Center, 90403 - Santa Monica/US
  • 4 Gu Postdoctoral Fellow, City of Hope Comprehensive Cancer Center, 91010 - Duarte/US
  • 5 Research, Mayo Clinic Cancer Center, 85054 - Phoenix/US
  • 6 Oncology Dept, Sarcoma Oncology Research Center, 90403 - Santa Monica/US
  • 7 Medical Oncology, Sarcoma Oncology Research Center, 90403 - Santa Monica/US

Resources

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Abstract 1729P

Background

Advanced soft tissue sarcoma is most often associated with a fatal outcome. This report provides an update on SAINT: A Phase I/Expanded Phase II Study Using Safe Amounts of Ipilimumab, Nivolumab and Trabectedin as First-Line Treatment of Advanced STS.

Methods

Primary: Evaluate best response rate by RECIST v1.1; Secondary: Assess progression-free survival (PFS) at 6 months and overall survival. Patients and Methods: Eligible patients for this Phase II study are males or females ≥ 18 years of age with locally advanced unresectable or metastatic soft tissue sarcoma, previously untreated, with measurable disease by RECIST v1.1. Treatment protocol: (I) 1 mg/kg i.v. q 12 wks, (N) 3 mg/kg i.v. q 2 wks, (T) 1.2 mg/m2 CIV q 3 wks.

Results

Ninety-seven patients were evaluated for efficacy. These subjects completed at least two treatment cycles and had at least one follow-up CT scan. The best responses were 6CR, 17PR, 57SD and 17PD with 24.7% ORR, 82.5% DCR. PFS rate at 6 months was 55%; Median PFS was 7.3 (95% CI: 5.247-9.353) months; Median OS was 32.0 (95% CI: 20.575- 43.425) months. The best responders (CR and PR) were patients with LMS, UPS, LPS, synovial, MFS, endometrial stromal, clear cell, DSRCT, spindle cell, and chondrosarcoma. Notably, out of the 97 patients who participated in the study between 2017 and 2024, 16 (17%) patients are still alive as of April 30, 2024, the data cut-off date. Grade 3/4 TRAEs related to Trabectedin include both hematologic and non- hematologic toxicities: fatigue, nausea, vomiting, fever, exhaustion, dehydration, asthenia, cellulitis of port, anemia, neutropenia, thrombocytopenia, transaminitis, elevated CK. There were no hematologic toxicities related to Nivolumab or Ipilimumab; Grade 3/4 TRAEs include decreased TSH, increased T4, increased TSH, transaminitis, hyponatremia, dehydration, pruritus, and psoriasis.

Conclusions

Taken together we have confirmed that (1) Trabectedin in combination with Ipilimumab and Nivolumab is a safe and effective regimen for previously untreated advanced STS, and (2) Randomized studies are needed to confirm whether this regimen is superior to standard first line therapy for advanced soft tissue sarcoma.

Clinical trial identification

NCT03138161.

Editorial acknowledgement

Legal entity responsible for the study

Sarcoma Oncology Research Center, LLC.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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