drugset / Trial / NCT01871766

Risk-Adapted Focal Proton Beam Radiation and/or Surgery in Patients With Low, Intermediate and High Risk Rhabdomyosarcoma Receiving Standard or Intensified Chemotherapy

NCT01871766

Phase 2 Active not recruiting 115 enrolled St. Jude Children's Research Hospital
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study will treat participants with newly diagnosed, low, intermediate and high risk rhabdomyosarcoma (RMS) using multi-modality risk-adapted therapy with standard or intensified dose chemotherapy, radiation and surgical resection. Intermediate and high risk participants will receive an additional 12 weeks (4 cycles) of maintenance therapy with anti-angiogenic chemotherapy. PRIMARY OBJECTIVE: * Estimate event-free survival for intermediate risk participants treated with vincristine, dactinomycin and cyclophosphamide with the addition of maintenance anti-angiogenic therapy. SECONDARY OBJECTIVES: * Estimate the false negative rate and incidence of additional positive lymph nodes in participants undergoing sentinel lymph node biopsy followed by limited nodal dissection. * Maintain a high local control rate in participants treated with surgery and/or limited volume proton and photon radiation without dose escalation. * Define the incidence and type of failure in participants who receive risk-adapted local therapy relative to the primary tumor volume. * Establish the feasibility of delivering 4 cycles of maintenance anti-angiogenic chemotherapy in intermediate and high risk patients following standard chemotherapy. * Estimate the event free survival for high risk patients receiving interval dose compressed therapy and maintenance anti-angiogenic therapy. * Define the incidence of CTC grade 3 and higher toxicities (and specific grade 1-2 toxicities) related to proton beam therapy.

Timeline

Start
2013-12-04
Primary completion
2026-12
Completion
2030-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 15 mg/kg Intravenous
Subject Cyclophosphamide Other / unclassified 40 mg/kg Intravenous
Subject Cyclophosphamide Other / unclassified 50 mg/m2 Intravenous
Subject Cyclophosphamide Other / unclassified 1200 mg/m2 Intravenous
Subject Dactinomycin Protein / enzyme biologic 0.025 mg/kg Intravenous
Subject Dactinomycin Protein / enzyme biologic 0.045 mg/kg Intravenous
Subject Doxorubicin Other / unclassified 18.75 mg/m2 Intravenous
Subject Doxorubicin Other / unclassified 37.5 mg/m2 Intravenous
Subject Etoposide Small molecule 100 mg/m2 Intravenous
Subject Ifosfamide Small molecule 1800 mg/m2 Intravenous
Subject Irinotecan Small molecule 50 mg/m2 Intravenous
Subject Sorafenib Small molecule 90 mg/m2
Subject Vincristine Small molecule 0.025 mg/kg Intravenous
Subject Vincristine Small molecule 0.05 mg/kg Intravenous
Subject Vincristine Small molecule 1.5 mg/m2 Intravenous
Background Dexrazoxane Small molecule 187.5 mg/m2 Intravenous
Background Dexrazoxane Small molecule 375 mg/m2 Intravenous
Background Pegfilgrastim Protein / enzyme biologic
Background filgrastim Protein / enzyme biologic 5 ug/kg Subcutaneous

Indications