A Prospective, Randomized, Controlled Clinical Study on the Prevention of Chemotherapy Related Myelosuppression in Patients with Ewing's Sarcoma Using Trilaciclib

PHASE2RecruitingINTERVENTIONAL
Enrollment

22

Participants

Timeline

Start Date

October 31, 2024

Primary Completion Date

September 30, 2026

Study Completion Date

September 30, 2027

Conditions
Ewing SarcomaMyelosuppression
Interventions
DRUG

Chemotherapy

Vincristine (V), intravenous injection, 1.5 mg/m2 (maximum not exceeding 2mg), D1, odd cycle administration Doxorubicin (D), intravenous infusion, 75mg/m2, D1, odd cycle administration When the cumulative dose of doxorubicin is ≥ 375mg/m2, replace it with actinomycin D 1.25mg/m2 Cyclophosphamide (C), intravenous infusion, 1200mg/m2, D1, odd cycle administration Ifosfamide (I), intravenous infusion, 1800mg/m2, D1-5, even cycle administration Etoposide (E), intravenous infusion, 100mg/m2, D1-5, even cycle administration

DRUG

Trilaciclib Injection [Cosela]

Trilaciclib, intravenous infusion, 240 mg/m2, administered following chemotherapy (2 hours after completion of vincristine administration and within 4 hours before administration of other chemotherapy drugs)

Trial Locations (1)

200032

RECRUITING

Fudan University Shanghai Cencer Center,, Shanghai

All Listed Sponsors
lead

Fudan University

OTHER