StudyFinder

COG ARST2031: A Randomized Phase 3 Trial of Vinorelbine, Dactinomycin, and Cyclophosphamide (VINO-AC) Plus Maintenance Chemotherapy with Vinorelbine and Oral Cyclophosphamide (VINO-CPO) vs Vincristine, Dactinomycin and Cyclophosphamide (VAC) plus VINO-CPO Maintenance in Patients with High Risk Rhabdomyosarcoma (HR-RMS)

Recruiting

This phase III trial compares the safety and effect of adding vinorelbine to vincristine, dactinomycin, and cyclophosphamide (VAC) for the treatment of patients with high risk rhabdomyosarcoma (RMS). High risk refers to cancer that is likely to recur (come back) after treatment or spread to other parts of the body. This study will also examine if adding maintenance therapy after VAC therapy, with or without vinorelbine, will help get rid of the cancer and/or lower the chance that the cancer comes back. Vinorelbine and vincristine are in a class of medications called vinca alkaloids. Dactinomycin is a type of antibiotic that is only used in cancer chemotherapy. Cyclophosphamide is in a class of medications called alkylating agents. Vinorelbine, vincristine, dactinomycin and cyclophosphamide are chemotherapy medications that work by slowing or stopping the growth of cancer cells in the body. This trial may have the potential to eliminate rhabdomyosarcoma for a long time or for the rest of patient's life.

I'm interested

Male or Female
Not specified
This study is NOT accepting healthy volunteers
Inclusion Criteria:

• up to 50 years old
• newly diagnosed (Rhabdomyosarcoma) RMS
• see link to clinicaltrials.gov for complete Inclusion and Exclusion Criteria
Exclusion Criteria:

• evidence of uncontrolled infection
• RMS that is considered a second cancer and previous cancer(s) that were treated with chemotherapy and/or radiation
• patients who have received any chemotherapy (excluding steroids) and/or radiation therapy for RMS
• women who are pregnant or breast feeding

Cancer, Cancer

Rhabdomyosarcoma, RMS

Allison Fullenkamp - fulle631@umn.edu
Emily Greengard
SITE00001780
See this study on ClinicalTrials.gov

Back