Surgical Outcome and Oncological Survival of Osteofibrous Dysplasia-Like and Classic Adamantinomas: An International Multicenter Study of 318 Cases.


Journal

The Journal of bone and joint surgery. American volume
ISSN: 1535-1386
Titre abrégé: J Bone Joint Surg Am
Pays: United States
ID NLM: 0014030

Informations de publication

Date de publication:
07 10 2020
Historique:
entrez: 7 10 2020
pubmed: 8 10 2020
medline: 20 4 2021
Statut: ppublish

Résumé

Osteofibrous dysplasia-like adamantinoma (OFD-AD) and classic adamantinoma (AD) are rare, neoplastic diseases with only limited data supporting current treatment protocols. We believe that our retrospective multicenter cohort study is the largest analysis of patients with adamantinoma to date. The primary purpose of this study was to describe the disease characteristics and evaluate the oncological outcomes. The secondary purpose was to identify risk factors for local recurrence after surgical treatment and propose treatment guidelines. Three hundred and eighteen confirmed cases of OFD-AD and AD for which primary treatment was carried out between 1985 and 2015 were submitted by 22 tertiary bone tumor centers. Proposed clinical risk factors for local recurrence such as size, type, and margins were analyzed using univariable and multivariate Cox regression analysis. Of the 318 cases, 128 were OFD-AD and 190 were AD. The mean age at diagnosis was 17 years (median, 14.5 years) for OFD-AD and 32 years (median, 28 years) for AD; 53% of the patients were female. The mean tumor size in the OFD-AD and AD groups combined was 7.8 cm, measured histologically. Sixteen percent of the patients sustained a pathological fracture prior to treatment. Local recurrence was recorded in 22% of the OFD-AD cases and 24% of the AD cases. None of the recurrences in the OFD-AD group progressed to AD. Metastatic disease was found in 18% of the AD cases and fatal disease, in 11% of the AD cases. No metastatic or fatal disease was reported in the OFD-AD group. Multivariate Cox regression analysis demonstrated that uncontaminated resection margins (hazard ratio [HR] = 0.164, 95% confidence interval [CI] = 0.092 to 0.290, p < 0.001), pathological fracture (HR = 1.968, 95% CI = 1.076 to 3.600, p = 0.028), and sex (female versus male: HR = 0.535, 95% CI = 0.300 to 0.952, p = 0.033) impacted the risk of local recurrence. OFD-AD and AD are parts of a disease spectrum but should be regarded as different entities. Our results support reclassification of OFD-AD into the intermediate locally aggressive category, based on the local recurrence rate of 22% and absence of metastases. In our study, metastatic disease was restricted to the AD group (an 18% rate). We advocate wide resection with uncontaminated margins including bone and involved periosteum for both OFD-AD and AD. Prognostic Level IV. See Instructions for Authors for a complete description of levels of evidence.

Sections du résumé

BACKGROUND
Osteofibrous dysplasia-like adamantinoma (OFD-AD) and classic adamantinoma (AD) are rare, neoplastic diseases with only limited data supporting current treatment protocols. We believe that our retrospective multicenter cohort study is the largest analysis of patients with adamantinoma to date. The primary purpose of this study was to describe the disease characteristics and evaluate the oncological outcomes. The secondary purpose was to identify risk factors for local recurrence after surgical treatment and propose treatment guidelines.
METHODS
Three hundred and eighteen confirmed cases of OFD-AD and AD for which primary treatment was carried out between 1985 and 2015 were submitted by 22 tertiary bone tumor centers. Proposed clinical risk factors for local recurrence such as size, type, and margins were analyzed using univariable and multivariate Cox regression analysis.
RESULTS
Of the 318 cases, 128 were OFD-AD and 190 were AD. The mean age at diagnosis was 17 years (median, 14.5 years) for OFD-AD and 32 years (median, 28 years) for AD; 53% of the patients were female. The mean tumor size in the OFD-AD and AD groups combined was 7.8 cm, measured histologically. Sixteen percent of the patients sustained a pathological fracture prior to treatment. Local recurrence was recorded in 22% of the OFD-AD cases and 24% of the AD cases. None of the recurrences in the OFD-AD group progressed to AD. Metastatic disease was found in 18% of the AD cases and fatal disease, in 11% of the AD cases. No metastatic or fatal disease was reported in the OFD-AD group. Multivariate Cox regression analysis demonstrated that uncontaminated resection margins (hazard ratio [HR] = 0.164, 95% confidence interval [CI] = 0.092 to 0.290, p < 0.001), pathological fracture (HR = 1.968, 95% CI = 1.076 to 3.600, p = 0.028), and sex (female versus male: HR = 0.535, 95% CI = 0.300 to 0.952, p = 0.033) impacted the risk of local recurrence.
CONCLUSIONS
OFD-AD and AD are parts of a disease spectrum but should be regarded as different entities. Our results support reclassification of OFD-AD into the intermediate locally aggressive category, based on the local recurrence rate of 22% and absence of metastases. In our study, metastatic disease was restricted to the AD group (an 18% rate). We advocate wide resection with uncontaminated margins including bone and involved periosteum for both OFD-AD and AD.
LEVEL OF EVIDENCE
Prognostic Level IV. See Instructions for Authors for a complete description of levels of evidence.

Identifiants

pubmed: 33027124
doi: 10.2106/JBJS.19.01056
pii: 00004623-202010070-00006
pmc: PMC8569856
mid: NIHMS1726352
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1703-1713

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Investigateurs

Reinhard Windhager (R)
Guido Scoccianti (G)
Eric Mascard (E)
Anthony Griffin (A)
Zhiping Deng (Z)
Andreas Krieg (A)
Olivera Calukovic (O)
Rianne Schoo (R)
Robert van der Wal (R)

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Auteurs

E M Schutgens (EM)

Departments of Orthopedic Surgery (E.M.S., P.D.S.D., and M.A.J.v.d.S.), Histopathology (J.V.M.G.B.), and Pathology (P.C.W.H.), Leiden University Medical Center, Leiden, the Netherlands.
London Sarcoma Service, Royal National Orthopaedic Hospital, Stanmore, United Kingdom.

P Picci (P)

Medical Oncology, Musculoskeletal Oncology Department, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.

D Baumhoer (D)

Bone Tumour Reference Centre, Institute of Pathology, University Hospital and University of Basel, Basel, Switzerland.

R Pollock (R)

London Sarcoma Service, Royal National Orthopaedic Hospital, Stanmore, United Kingdom.

J V M G Bovée (JVMG)

Departments of Orthopedic Surgery (E.M.S., P.D.S.D., and M.A.J.v.d.S.), Histopathology (J.V.M.G.B.), and Pathology (P.C.W.H.), Leiden University Medical Center, Leiden, the Netherlands.

P C W Hogendoorn (PCW)

Departments of Orthopedic Surgery (E.M.S., P.D.S.D., and M.A.J.v.d.S.), Histopathology (J.V.M.G.B.), and Pathology (P.C.W.H.), Leiden University Medical Center, Leiden, the Netherlands.

P D S Dijkstra (PDS)

Departments of Orthopedic Surgery (E.M.S., P.D.S.D., and M.A.J.v.d.S.), Histopathology (J.V.M.G.B.), and Pathology (P.C.W.H.), Leiden University Medical Center, Leiden, the Netherlands.

A J Rueten-Budde (AJ)

Mathematical Institute, Leiden University, Leiden, the Netherlands.

P C Jutte (PC)

Department of Orthopedics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

F Traub (F)

Orthopedic Surgery, University of Tübingen, Tübingen, Germany.

A Leithner (A)

Department of Orthopedics and Trauma, Medical University of Graz, Graz, Austria.

P-U Tunn (PU)

Orthopedic Surgery, Helios-Clinics, Berlin, Germany.

P Funovics (P)

Orthopedic Surgery, Medical University of Vienna, Vienna, Austria.

G Sys (G)

Orthopedic Surgery, Ghent University Hospital, Ghent, Belgium.

M San-Julian (M)

Orthopedic Surgery, University of Navarra, Pamplona, Spain.

G R Schaap (GR)

Orthopedic Surgery, Academic Medical Center, Amsterdam, the Netherlands.

H R Dürr (HR)

Department of Tumor Orthopedics and Sarcoma Surgery, University Hospital Essen, Essen, Germany.

J Hardes (J)

Musculoskeletal Oncology, Department of Orthopedic Surgery, Physical Medicine and Rehabilitation, University Hospital, LMU Munich, Munich, Germany.

J Healey (J)

Orthopedic Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.

R Capanna (R)

Department of Orthopaedics, S. Chiara University Hospital, University of Pisa, Italy.

D Biau (D)

Orthopedic Surgery, Cochin Hospital, Paris, France.

A Gomez-Brouchet (A)

Department of Histopathology, University Medical Center, Toulouse, France.

J Wunder (J)

University Musculoskeletal Oncology Unit, Mount Sinai Hospital, Toronto, Ontario, Canada.

T D A Cosker (TDA)

Orthopedic Surgery, Nuffield Orthopedic Center, Oxford, United Kingdom.

M K Laitinen (MK)

Orthopedic Surgery, Helsinki University Hospital, Helsinki, Finland.

X Niu (X)

Department of Orthopedic Oncology, Beijing Jishuitan Hospital, Beijing, People's Republic of China.

V Kostiuk (V)

Orthopedic Surgery, National Cancer Institute Ukraine, Kiev, Ukraine.

M A J van de Sande (MAJ)

Departments of Orthopedic Surgery (E.M.S., P.D.S.D., and M.A.J.v.d.S.), Histopathology (J.V.M.G.B.), and Pathology (P.C.W.H.), Leiden University Medical Center, Leiden, the Netherlands.

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