Vinorelbine and continuous low-dose cyclophosphamide as maintenance chemotherapy in patients with high-risk rhabdomyosarcoma (RMS 2005): a multicentre, open-label, randomised, phase 3 trial

• Published in: The lancet oncology 2019-11, Vol.20 (11), p.1566-1575
• Main Authors: Bisogno, Gianni, De Salvo, Gian Luca, Bergeron, Christophe, Gallego Melcón, Soledad, Merks, Johannes H, Kelsey, Anna, Martelli, Helene, Minard-Colin, Veronique, Orbach, Daniel, Glosli, Heidi, Chisholm, Julia, Casanova, Michela, Zanetti, Ilaria, Devalck, Christine, Ben-Arush, Myriam, Mudry, Peter, Ferman, Sima, Jenney, Meriel, Ferrari, Andrea
• Format: Article
• Language: English
• Subjects: Adolescent; Age; Alveoli; Antidiuretics; Antineoplastic Combined Chemotherapy Protocols - administration & dosage; Antineoplastic Combined Chemotherapy Protocols - adverse effects; Argentina; Brazil; Chemotherapy; Child; Clinical trials; Cyclophosphamide; Cyclophosphamide - administration & dosage; Cyclophosphamide - adverse effects; Dactinomycin; Disease Progression; Disease-Free Survival; Doxorubicin; Europe; Female; Gait; Hematology; Humans; Ifosfamide; Intravenous administration; Israel; Leukopenia; Lymphatic system; Maintenance Chemotherapy - adverse effects; Maintenance Chemotherapy - mortality; Male; Medical prognosis; Menopause; Metastases; Metastasis; Neurotoxicity; Neutropenia; Patients; Prostate; Remission; Remission Induction; Rhabdomyosarcoma; Rhabdomyosarcoma, Alveolar - drug therapy; Rhabdomyosarcoma, Alveolar - mortality; Rhabdomyosarcoma, Alveolar - pathology; Rhabdomyosarcoma, Embryonal - drug therapy; Rhabdomyosarcoma, Embryonal - mortality; Rhabdomyosarcoma, Embryonal - pathology; Risk Assessment; Risk Factors; Risk groups; Secretion; Soft tissue sarcoma; Studies; Surgery; Survival; Thrombocytopenia; Time Factors; Tumors; Vinorelbine - administration & dosage; Vinorelbine - adverse effects; Young Adult
• ISSN: 1470-2045; 1474-5488
• DOI: 10.1016/S1470-2045(19)30617-5

For more than three decades, standard treatment for rhabdomyosarcoma in Europe has included 6 months of chemotherapy. The European paediatric Soft tissue sarcoma Study Group (EpSSG) aimed to investigate whether prolonging treatment with maintenance chemotherapy would improve survival in patients with high-risk rhabdomyosarcoma. RMS 2005 was a multicentre, open-label, randomised, controlled, phase 3 trial done at 102 hospitals in 14 countries. We included patients aged 6 months to 21 years with rhabdomyosarcoma who were considered to be at high risk of relapse: those with non-metastatic incompletely resected embryonal rhabdomyosarcoma occurring at unfavourable sites with unfavourable age (≥10 years) or tumour size (>5 cm), or both; those with any non-metastatic rhabdomyosarcoma with nodal involvement; and those with non-metastatic alveolar rhabdomyosarcoma but without nodal involvement. Patients in remission after standard treatment (nine cycles of ifosfamide, vincristine, dactinomycin with or without doxorubicin, and surgery or radiotherapy, or both) were randomly assigned (1:1) to stop treatment or continue maintenance chemotherapy (six cycles of intravenous vinorelbine 25 mg/m2 on days 1, 8, and 15, and daily oral cyclophosphamide 25 mg/m2, on days 1–28). Randomisation was done by use of a web-based system and was stratified (block size of four) by enrolling country and risk subgroup. Neither investigators nor patients were masked to treatment allocation. The primary outcome was disease-free survival in the intention-to-treat population. Secondary outcomes were overall survival and toxicity. This trial is registered with EudraCT, number 2005-000217-35, and ClinicalTrials.gov, number NCT00339118, and follow-up is ongoing. Between April 20, 2006, and Dec 21, 2016, 371 patients were enrolled and randomly assigned to the two groups: 186 to stop treatment and 185 to receive maintenance chemotherapy. Median follow-up was 60·3 months (IQR 32·4–89·4). In the intention-to-treat population, 5-year disease-free survival was 77·6% (95% CI 70·6–83·2) with maintenance chemotherapy versus 69·8% (62·2–76·2) without maintenance chemotherapy (hazard ratio [HR] 0·68 [95% CI 0·45–1·02]; p=0·061), and 5-year overall survival was 86·5% (95% CI 80·2–90·9) with maintenance chemotherapy versus 73·7% (65·8–80·1) without (HR 0·52 [95% CI 0·32–0·86]; p=0·0097). Toxicity was manageable in patients who received maintenance chemotherapy: 136 (75%) of 181 patients had grade 3–4 leucope