Periosteal osteosarcoma - a European review of outcome

被引:54
作者
Grimer, RJ
Bielack, S
Flege, S
Cannon, SR
Foleras, G
Andreeff, I
Sokolov, T
Taminiau, A
Dominkus, M
San-Julian, M
Kollender, Y
Gosheger, G
机构
[1] Royal Orthopaed Hosp, Royal Orthopaed Hosp, Oncol Serv, Birmingham B31 2AP, W Midlands, England
[2] Univ Childrens Hosp, COSS, Dept Paediat Haematol & Oncol, Munster, Germany
[3] Royal Natl Orthopaed Hosp, London W1N 6AD, England
[4] Norwegian Radium Hosp, Oslo, Norway
[5] Univ Sofia, Hosp Orthopaed, BU-1126 Sofia, Bulgaria
[6] Leiden Univ, Med Ctr, Leiden, Netherlands
[7] Univ Vienna, Sch Med, Vienna, Austria
[8] Univ Navarra, Navarra, Spain
[9] Tel Aviv Sourasky Med Ctr, Tel Aviv, Israel
[10] Univ Munster, Munster, Germany
关键词
periosteal osteosarcoma; chemotherapy; local recurrence; outcome;
D O I
10.1016/j.ejca.2005.04.052
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Periosteal osteosarcoma is a rare primary malignant bone tumour. Treatment is by surgical excision, but controversy remains about the value of chemotherapy. The members of the European Musculo Skeletal Oncology Society (EMSOS) collaborated to produce a dataset of 119 patients. The predominant site for the tumour was the femur, followed by the tibia. All but 2 patients underwent surgery, with 9 requiring amputation and the others having limb salvage. A total of 81 patients had chemotherapy, of whom 50 had neoadjuvant chemotherapy. There was no standard chemotherapy regime, but all patients receiving chemotherapy were given doxorubicin combined with at least one other agent. The overall survival was 89% at 5 years and 83% at 10 years. Eight patients developed local recurrence, of whom 5 died. Survival was related to appearance of local recurrence (P < 0.0001) but no other single factor. The use of chemotherapy was not shown to be a prognostic factor, but was used in two-thirds of the patients in this study. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2806 / 2811
页数:6
相关论文
共 20 条
[1]   Second malignant neoplasms in long-term survivors of osteosarcoma - Memorial sloan-kettering cancer center experience [J].
Aung, L ;
Gorlick, RG ;
Shi, W ;
Thaler, H ;
Shorter, NA ;
Healey, JH ;
Huvos, AG ;
Meyers, PA .
CANCER, 2002, 95 (08) :1728-1734
[2]  
CAMPANACCI M, 1976, Italian Journal of Orthopaedics and Traumatology, V2, P23
[3]  
Campanacci M., 1999, BONE SOFT TISSUE TUM
[4]  
COX DR, 1972, J R STAT SOC B, V34, P187
[5]  
Ewing J., 1939, B AM COLL SURG, V24, P290, DOI [10.1001/archsurg.1922.01110120002001, DOI 10.1001/ARCHSURG.1922.01110120002001]
[6]  
Fletcher DM., 2002, PATHOLOGY GENETICS T, V3
[7]  
HALL RB, 1985, CANCER, V55, P165
[8]  
JOZSA LG, 2002, HUNGARIAN ONCOL, V46, P271
[9]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481
[10]  
LICHTENSTEIN L, 1955, CANCER, V8, P1060, DOI 10.1002/1097-0142(1955)8:5<1060::AID-CNCR2820080533>3.0.CO