RMS2005 was an international study coordinated by the European pediatric Soft tissue sarcoma Study Group (EpSSG) dedicated to children and adolescents (0-25 years) with nonmetastatic rhabdomyosarcoma (RMS). Patients were allocated to four different groups: low risk (LR), standard risk (SR), high risk (HR), and very high risk (VHR). Patients in LR, SR, and VHR were enrolled in three different observational studies partially published.1,2 HR patients were included in two consecutive randomized trials that demonstrated doxorubicin can be safely omitted from standard chemotherapy and a survival advantage from adding maintenance chemotherapy to standard treatment.
The study was open from October 1st, 2005, to December 31st, 2016 and 1,733 patients were enrolled from 14 countries (Argentina, Belgium, Brazil, Czech Republic, France, Ireland, Israel, Italy, Norway, Switzerland, Slovenia, Spain, The Netherlands, and United Kingdom).
After a median followup of 73.1 months, the 5-year event-free survival (EFS) and overall survival (OS) of the 1,733 patients enrolled were 70.7% and 80.4%, respectively. The results by subgroup: LR (80 patients) EFS 93.7%, OS 96.7%; SR (652 patients) EFS 77.4%, OS 90.6%; HR (851 patients) EFS 67.3%, OS 76.7%; and VHR (150 patients) EFS 48.8%, OS 49.7%. The study demonstrated that around 80% of patients with nonmetastatic RMS are long-term survivors, partly explained by the excellent outcome of LR and SR patients (42.2% of the population), with long-term survival rates above 90%. The LR group results demonstrate that the criteria we used identify a selected group (4.6% of patients) that can be treated with relatively short, low-toxic chemotherapy.
The RMS 2005 trial has modified the existing European standard proposing: (1) a 22-week alkylating-free regimen for LR patients, (2) the reduction of the cumulative dose of ifosfamide in the SR group, (3) the omission of anthracyclines in HR patients (4) 27 weeks of standard chemotherapy (ifosfamide, vincristine and actinomycn D), with the addition of maintenance chemotherapy for HR patients.
The contribution of Modesto Carli (Padova), Odile Oberlin (Paris) and Michele Steven (Bristol) must be acknowledged. With their work and vision, they created the EpSSG, making the RMS 2005 and RMS 2008 trials possible.
The study was open from October 1st, 2005, to December 31st, 2016 and 1,733 patients were enrolled from 14 countries (Argentina, Belgium, Brazil, Czech Republic, France, Ireland, Israel, Italy, Norway, Switzerland, Slovenia, Spain, The Netherlands, and United Kingdom).
After a median followup of 73.1 months, the 5-year event-free survival (EFS) and overall survival (OS) of the 1,733 patients enrolled were 70.7% and 80.4%, respectively. The results by subgroup: LR (80 patients) EFS 93.7%, OS 96.7%; SR (652 patients) EFS 77.4%, OS 90.6%; HR (851 patients) EFS 67.3%, OS 76.7%; and VHR (150 patients) EFS 48.8%, OS 49.7%. The study demonstrated that around 80% of patients with nonmetastatic RMS are long-term survivors, partly explained by the excellent outcome of LR and SR patients (42.2% of the population), with long-term survival rates above 90%. The LR group results demonstrate that the criteria we used identify a selected group (4.6% of patients) that can be treated with relatively short, low-toxic chemotherapy.
The RMS 2005 trial has modified the existing European standard proposing: (1) a 22-week alkylating-free regimen for LR patients, (2) the reduction of the cumulative dose of ifosfamide in the SR group, (3) the omission of anthracyclines in HR patients (4) 27 weeks of standard chemotherapy (ifosfamide, vincristine and actinomycn D), with the addition of maintenance chemotherapy for HR patients.
The contribution of Modesto Carli (Padova), Odile Oberlin (Paris) and Michele Steven (Bristol) must be acknowledged. With their work and vision, they created the EpSSG, making the RMS 2005 and RMS 2008 trials possible.
Coordinating Investigator RMS 2005
Prof. Gianni BisognoDepartment of Women’s and children’s health, University of Padova,
via Giustiniani, 3 - 35128 Padova, Italia
Name | Country | Hospital |
---|---|---|
Current Members | ||
Gianni Bisogno | Italy | Haematology/Oncology Division, University of Padova, Padova |
Meriel Jenney | UK | Children’s Hospital for Wales, Heath Park, Cardiff |
Soledad Gallego | Spain | Department of Pediatric Surgery, Hospital Universitari Vall d'Hebron,Barcelona |
Christophe Bergeron | France | Institute of Pediatric Hematology and Oncology, Center Leon Berard,Lyon |
Veronique Minard-Colin | France | Department of Pediatric and Adolescent Oncology, Gustave-Roussy, Villejuif |
Henry Mandeville | United Kingdom | Royal Marsden Hospital and Institute of Cancer Research, Sutton |
Andrea Ferrari | Italy | Pediatric Oncology Unit, Istituto Nazionale Tumori, Milano |
Helene Martelli | France | Service de Chirurgie Pediatrique, Hopital de Bicetre |
Anna Kelsey | United Kingdom | Dept. of Paediatric Hiistopathology, Manchester University, NHS Foundation Trust |
Gian Luca De Salvo | Italy | IOV Veneto Oncology Institute, Padova |