Your browser doesn't support javascript.
loading
EURAMOS-1, an international randomised study for osteosarcoma: results from pre-randomisation treatment.
Whelan, J S; Bielack, S S; Marina, N; Smeland, S; Jovic, G; Hook, J M; Krailo, M; Anninga, J; Butterfass-Bahloul, T; Böhling, T; Calaminus, G; Capra, M; Deffenbaugh, C; Dhooge, C; Eriksson, M; Flanagan, A M; Gelderblom, H; Goorin, A; Gorlick, R; Gosheger, G; Grimer, R J; Hall, K S; Helmke, K; Hogendoorn, P C W; Jundt, G; Kager, L; Kuehne, T; Lau, C C; Letson, G D; Meyer, J; Meyers, P A; Morris, C; Mottl, H; Nadel, H; Nagarajan, R; Randall, R L; Schomberg, P; Schwarz, R; Teot, L A; Sydes, M R; Bernstein, M.
Afiliação
  • Whelan JS; Department of Oncology, University College Hospital, London, UK.
  • Bielack SS; Cooperative Osteosarcoma Study Group (COSS), Klinikum Stuttgart - Olgahospital, Stuttgart, Germany.
  • Marina N; Stanford University Medical Center, Pediatric Hematology/Oncology, Palo Alto, USA.
  • Smeland S; Division of Cancer, Surgery and Transplantation, and Scandinavian Sarcoma Group, Oslo University Hospital, Oslo Institute for Clinical Medicine, University of Oslo, Oslo, Norway.
  • Jovic G; Medical Research Council Clinical Trials Unit at University College London, London, UK.
  • Hook JM; Medical Research Council Clinical Trials Unit at University College London, London, UK.
  • Krailo M; Children's Oncology Group, Arcadia, USA.
  • Anninga J; Department of Pediatrics and Medical Oncology, Leiden University Medical Center, Leiden, The Netherlands.
  • Butterfass-Bahloul T; Center for Clinical Trials, University Hospital Münster, Münster, Germany.
  • Böhling T; University of Helsinki and HUSLAB, Helsinki, Finland.
  • Calaminus G; University Hospital of Muenster, Muenster, Germany.
  • Capra M; Our Lady's Children's Hospital, Dublin, Ireland.
  • Deffenbaugh C; Lucile Salter Packard Childrens Hospital Stanford, Palo Alto, USA.
  • Dhooge C; University Hospital Ghent, Gent, Belgium.
  • Eriksson M; Skane University Hospital, Lund University, Lund, Sweden.
  • Flanagan AM; Royal National Orthopaedic Hospital, Stanmore Cancer Institute, University College London, London, UK.
  • Gelderblom H; Department of Pediatrics and Medical Oncology, Leiden University Medical Center, Leiden, The Netherlands.
  • Goorin A; Dana-Farber Cancer Institute, Boston.
  • Gorlick R; Section of Pediatric Hematology/Oncology, Montefiore Medical Center, Bronx, USA.
  • Gosheger G; Department of General Orthopedics and Tumor Orthopedics, University Hospital Muenster, Muenster, Germany.
  • Grimer RJ; Royal Orthopaedic Hospital, Birmingham, UK.
  • Hall KS; Department of Oncology, Oslo University Hospital, Norwegian Radium Hospital, Scandinavian Sarcoma Group, Oslo, Norway.
  • Helmke K; Department of Pediatric Radiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Hogendoorn PC; Department of Pediatrics and Medical Oncology, Leiden University Medical Center, Leiden, The Netherlands.
  • Jundt G; Bone Tumor Reference Center at the Institute of Pathology, University Hospital Basel, Basel, Switzerland.
  • Kager L; St Anna Children's Hospital, Vienna, Austria.
  • Kuehne T; University Children's Hospital Basel, Basel, Switzerland.
  • Lau CC; Texas Children's Cancer Centre, Baylor College of Medicine, Houston.
  • Letson GD; H. Lee Moffit Cancer Centre & Research Institute, Tampa.
  • Meyer J; Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia.
  • Meyers PA; Memorial Sloan-Kettering Cancer Center, New?York.
  • Morris C; Memorial Sloan-Kettering Cancer Center, New?York Orthopedic Surgery, Johns Hopkins, Baltimore, USA.
  • Mottl H; Department of Pediatric Hematology Oncology, University Hospital, Prague, Czech Republic.
  • Nadel H; British Columbia Children's Hospital, University of British Columbia, Vancouver, Canada.
  • Nagarajan R; Cincinnati Children's Hospital Medical Center, Cincinnati.
  • Randall RL; Primary Children's Hospital and Huntsman Cancer Institute, University of Utah, Salt Lake City.
  • Schomberg P; Mayo Clinic, Rochester, USA.
  • Schwarz R; Department of Radiation Oncology, Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Teot LA; Department of Pathology, Boston Children's Hospital, Boston, USA.
  • Sydes MR; Medical Research Council Clinical Trials Unit at University College London, London, UK m.sydes@ucl.ac.uk.
  • Bernstein M; IWK Health Center, Dalhousie University, Halifax, Canada.
Ann Oncol ; 26(2): 407-14, 2015 Feb.
Article em En | MEDLINE | ID: mdl-25421877
ABSTRACT

BACKGROUND:

Four international study groups undertook a large study in resectable osteosarcoma, which included two randomised controlled trials, to determine the effect on survival of changing post-operative chemotherapy based on histological response. PATIENTS AND

METHODS:

Patients with resectable osteosarcoma aged ≤40 years were treated with the MAP regimen, comprising pre-operatively of two 5-week cycles of cisplatin 120 mg/m(2), doxorubicin 75 mg/m(2), methotrexate 12 g/m(2) × 2 (MAP) and post-operatively two further cycles of MAP and two cycles of just MA. Patients were randomised after surgery. Those with ≥10% viable tumour in the resected specimen received MAP or MAP with ifosfamide and etoposide. Those with <10% viable tumour were allocated to MAP or MAP followed by pegylated interferon. Longitudinal evaluation of quality of life was undertaken.

RESULTS:

Recruitment was completed to the largest osteosarcoma study to date in 75 months. Commencing March 2005, 2260 patients were registered from 326 centres across 17 countries. About 1334 of 2260 registered patients (59%) were randomised. Pre-operative chemotherapy was completed according to protocol in 94%. Grade 3-4 neutropenia affected 83% of cycles and 59% were complicated by infection. There were three (0.13%) deaths related to pre-operative chemotherapy. At definitive surgery, 50% of patients had at least 90% necrosis in the resected specimen.

CONCLUSIONS:

New models of collaboration are required to successfully conduct trials to improve outcomes of patients with rare cancers; EURAMOS-1 demonstrates achievability. Considerable regulatory, financial and operational challenges must be overcome to develop similar studies in the future. The trial is registered as NCT00134030 and ISRCTN 67613327.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ósseas / Protocolos de Quimioterapia Combinada Antineoplásica / Osteossarcoma Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ósseas / Protocolos de Quimioterapia Combinada Antineoplásica / Osteossarcoma Idioma: En Ano de publicação: 2015 Tipo de documento: Article