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Feasibility of Atezolizumab in Combination With Chemotherapy for Children With Relapsed or Refractory Solid Tumors.

作者信息

Campbell Matthew E, Stutzman Sonja, Primeaux Sharon, Sida Deseray, Lee Minjae, Shah Avanthi T, Sadanand Arhanti, Sokol Elizabeth, Collins Natalie B, Turpin Brian, Navai Shoba, Albert Katie, Laetsch Theodore W, Rakheja Dinesh, Chen Kenneth S, Gerber David E, Koh Andrew Y

机构信息

Division of Hematology/Oncology, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Department of Health Data Science & Biostatistics, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

出版信息

Pediatr Blood Cancer. 2025 Sep 12:e32046. doi: 10.1002/pbc.32046.

Abstract

BACKGROUND

Combining immune checkpoint inhibitors (ICI) with chemotherapy may improve treatment response in children with solid tumors. We sought to determine the feasibility of combining vincristine, irinotecan, and temozolomide with the ICI atezolizumab in children with relapsed or refractory solid tumors (VITAS;).

METHODS

Patients ≥6 months and ≤18 years old with a relapsed or refractory solid tumor, no prior ICI, and evaluable disease per RECIST v1.1 were eligible for the Phase I cohort (NCT04796012). Patients received atezolizumab 15 mg/kg on Day 1, vincristine 1.5 mg/m on Day 1, irinotecan 50 mg/m on Days 1-5, and temozolomide 100 mg/m on Days 1-5 in 21-day cycles. The primary endpoint was the number of patients with dose-limiting toxicities (DLT) in the first two cycles of therapy.

RESULTS

Six patients (median age: 14 years) with rhabdomyosarcoma (n = 3), osteosarcoma (n = 2), and Ewing sarcoma (n = 1) received therapy and were evaluable for toxicity. Patients received a median of seven (range: 2-20) cycles of treatment. No patients experienced a DLT. One patient experienced Grade 2 immune-related colitis. Four patients experienced Grade ≥3 adverse events (decreased neutrophil count, febrile neutropenia, weight loss, anorexia). One patient with rhabdomyosarcoma had a sustained partial response through 16 cycles. One patient with relapsed pulmonary osteosarcoma has ongoing stable disease through 20 cycles.

CONCLUSIONS

Atezolizumab combined with vincristine, irinotecan, and temozolomide was feasible and well tolerated in children with solid tumors. Efficacy of this regimen is now being assessed in relapsed and refractory rhabdomyosarcoma in an ongoing Phase II cohort.

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