Incidence, Predictive Factors, and Prognosis of Chondrosarcoma in Patients with Ollier Disease and Maffucci Syndrome: An International Multicenter Study of 161 Patients

Author:

Verdegaal Suzan H.M.1,Bovée Judith V.M.G.1,Pansuriya Twinkal C.1,Grimer Robert J.2,Ozger Harzem3,Jutte Paul C.4,San Julian Mikel5,Biau David J.6,Geest Ingrid C.M.7,Leithner Andreas8,Streitbürger Arne9,Klenke Frank M.10,Gouin Francois G.11,Campanacci Domenico A.12,Marec-Berard Perrine13,Hogendoorn Pancras C.W.1,Brand Ronald1,Taminiau Antonie H.M.1

Affiliation:

1. a Leiden University Medical Center, Leiden, The Netherlands;

2. b Royal Orthopaedic Hospital, Birmingham, United Kingdom;

3. c Istanbul Tip Fak Capa-FATIH, Istanbul, Turkey;

4. d University Medical Centre Groningen, Groningen, The Netherlands;

5. e Clinica Universitaria de Navarra, Pamplona, Spain;

6. f Hôpital Cochin, Paris, France;

7. g Radboud University Medical Centre, Nijmegen, The Netherlands;

8. h Department of Orthopaedic Surgery, Medical University of Graz, Graz, Austria;

9. i Klinik und Poliklinik für Allgemeiner Orthopädie Uniklinik Münster, Münster, Germany;

10. j Inselspital, University of Bern, Bern, Switzerland;

11. k Hotel-Dieu, Nantes, France;

12. l Orthopaedic Oncology Unit, Azienda Ospedaliera Universitaria Careggi, Firenze, Italy;

13. m Institut d'Hématologie et d'Oncologie Pediatrique, Lyon, France

Abstract

Abstract Learning Objectives After completing this course, the reader will be able to: Describe major enchondroma distribution patterns that were identified in this study.Identify variables that are predictive for the secondary transformation of enchondroma over the lifetime of individuals with Ollier disease or Maffucci syndrome. CME This article is available for continuing medical education credit at CME.TheOncologist.com Background. Enchondromatosis is characterized by the presence of multiple benign cartilage lesions in bone. While Ollier disease is typified by multiple enchondromas, in Maffucci syndrome these are associated with hemangiomas. Studies evaluating the predictive value of clinical symptoms for development of secondary chondrosarcoma and prognosis are lacking. This multi-institute study evaluates the clinical characteristics of patients, to get better insight on behavior and prognosis of these diseases. Method. A retrospective study was conducted using clinical data of 144 Ollier and 17 Maffucci patients from 13 European centers and one national databank supplied by members of the European Musculoskeletal Oncology Society. Results. Patients had multiple enchondromas in the hands and feet only (group I, 18%), in long bones including scapula and pelvis only (group II, 39%), and in both small and long/flat bones (group III, 43%), respectively. The overall incidence of chondrosarcoma thus far is 40%. In group I, only 4 patients (15%) developed chondrosarcoma, in contrast to 27 patients (43%) in group II and 26 patients (46%) in group III, respectively. The risk of developing chondrosarcoma is increased when enchondromas are located in the pelvis (odds ratio, 3.8; p = 0.00l). Conclusions. Overall incidence of development of chondrosarcoma is 40%, but may, due to age-dependency, increase when considered as a lifelong risk. Patients with enchondromas located in long bones or axial skeleton, especially the pelvis, have a seriously increased risk of developing chondrosarcoma, and are identified as the population that needs regular screening on early detection of malignant transformation.

Funder

The Netherlands Organization for Scientific Research

EuroBoNet

Network of Excellence for studying Bone Tumours

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Reference39 articles.

1. Dyschondroplasie;Ollier;Lyon Med,1900

2. Di un caso encondroma ed angioma multiplo;Maffucci;Mov Med Chir (Napoli),1881

3. Enchondromatosis: Insights on the different subtypes;Pansuriya;Int J Clin Exp Pathol,2010

4. Cartilage tumours and bone development: Molecular pathology and possible therapeutic targets;Bovée;Nat Rev Cancer,2010

5. Emerging pathways in the development of chondrosarcoma of bone and implications for targeted treatment;Bovée;Lancet Oncol,2005

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