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Case Report: Relapsed alveolar rhabdomyosarcoma treated with abemaciclib, temozolomide, and irinotecan in the JPCS
Antonio Juan Ribelles1, Nuria Benavent2, Daniel Sanchez Mateos3
1Pediatric Oncology and Hematology Unit, University Hospital and Polytechnic La Fe, Valencia, Spain.
Background:
Cyclin-dependent kinase (CDK) 4 and CDK6 play fundamental roles in cell cycle progression. The CDK4/6 inhibitor abemaciclib, in combination with temozolomide and irinotecan, was evaluated in pediatric and young adult patients with relapsed/refractory solid tumors in the phase 1b dose-escalation study, JPCS Part A (NCT04238819). This case report describes the notable results of a patient with relapsed alveolar rhabdomyosarcoma (ARMS) who experienced a prolonged complete response.
Case Presentation:
An 8-year-old White male was initially diagnosed with stage IV ARMS with PAX3-FOXO1 fusion. Molecular characterization following a fourth relapse revealed CDK4, ERBB3, GLI1, MYCN, and FGFR4 amplifications and MYCN mutation. After five relapses, the patient enrolled in JPCS Part A and received abemaciclib (55 mg/m2 twice daily continuously) in combination with temozolomide (100 mg/m2 daily) and irinotecan (50 mg/m2 daily) on days 1 to 5 of 21-day cycles. The patient received 12 cycles of the triplet combination, followed by 23 additional cycles of abemaciclib monotherapy. Complete response (CR) was achieved in less than 3 months, with a duration of response (DOR) of 22.6 months and progression-free survival (PFS) of 23.7 months. The study treatment was well tolerated.
Conclusion:
CDK4/6 inhibition with abemaciclib in combination with temozolomide and irinotecan provided a durable response in a patient with heavily pretreated ARMS. Additional studies may be warranted to further understand the role of CDK4/6 inhibitors for treatment of ARMS.
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