Neoadjuvant chemotherapy with doxorubicin and cisplatin in malignant fibrous histiocytoma of bone: A European osteosarcoma intergroup study

被引:51
作者
Bramwell, VHC
Steward, WP
Nooij, M
Whelan, J
Craft, AW
Grimer, RJ
Taminau, AHM
Cannon, SR
Malcolm, AJ
Hogendoorn, PCW
Uscinska, B
Kirkpatrick, AL
Machin, D
Van Glabbeke, MM
机构
[1] London Reg Canc Ctr, London, ON N6A 4L6, Canada
[2] Leicester Royal Infirm, Leicester, Leics, England
[3] UCL Hosp Natl Hlth Serv Trust, London, England
[4] Royal Victoria Infirm, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[5] Royal Orthopaed Hosp Natl Hlth Serv Trust, Birmingham, W Midlands, England
[6] Royal Natl Orthopaed Hosp, London W1N 6AD, England
[7] MRC, Canc Trials Off, Cambridge, England
[8] Leiden Univ, Med Ctr, Leiden, Netherlands
[9] European Org Res Treatment Canc, Ctr Data, Brussels, Belgium
关键词
D O I
10.1200/JCO.1999.17.10.3260
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Studies involving small ease series have suggested that malignant fibrous histiocytoma of bone (MFH-B) is a chemosensitive tumor and that chemotherapy may improve survival, In this study, we evaluated clinical and pathologic response rates and survival in a series of patients treated with a consistent chemotherapy regimen of doxorubicin and cisplatin (DOX/DDP), Patients and Methods: Study patients were required to have biopsy-proven MFH-B, no previous chemotherapy, and primary or metastatic measurable disease and to be less than or equal to 65 years of age, Treatment consisted of doxorubicin 25 mg/m(2)/d days 1 through 3 and cisplatin 100 mg/m(2) by 4-hour intravenous infusion every 3 weeks for six cycles. In patients with operable primary tumors, chemotherapy was planned to start within 42 days of biopsy, with definitive surgery performed after three cycles. Results: Forty-one patients herd operable nonmetastatic limb sarcomas, and 23 (56%) completed six chemotherapy cycles. Limb salvage was possible in 33 patients (80%), and 16 (42%) of 38 assessable specimens showed a good pathologic response (greater than or equal to 90% necrosis), Median time to progression was 56 months, and the 5-year progression-free survival rate was 56% (95% confidence interval [CI], 40% to 72%). Median survival time war 63 months, and the 5-year survival rate was 59% (95% CI, 41% to 77%). Patients with a good pathologic response had longer survival times and times to progression than did those with a poor response. Also treated were two patients with locally recurrent and nine with metastatic disease, and these patients had a median survival time of 17.5 months. Conclusion: Our study suggests that adjuvant or neoadjuvant chemotherapy with DOX/DDP is beneficial in MFH-B, Good pathologic response rates and survivors are quite comparable with those far osteosarcoma, a related bone tumor for which adjuvant or neoadjuvant chemotherapy is an accepted practice. (C) 1999 by American Society of Clinical Oncology.
引用
收藏
页码:3260 / 3269
页数:10
相关论文
共 48 条
  • [1] Bacci G, 1996, Chir Organi Mov, V81, P139
  • [2] BACCI G, 1988, CHEMIOTERAPIA, V7, P406
  • [3] Neoadjuvant chemotherapy for osseous malignant fibrous histiocytoma of the extremity: Results in 18 cases and comparison with 112 contemporary osteosarcoma patients treated with the same chemotherapy regimen
    Bacci, G
    Ferrari, S
    Bertoni, F
    Mercuri, M
    Forni, C
    Sottili, S
    Gasbarrini, A
    Tienghi, A
    Cesari, M
    Campanacci, M
    [J]. JOURNAL OF CHEMOTHERAPY, 1997, 9 (04) : 293 - 299
  • [4] A COMPARISON OF 2 SHORT INTENSIVE ADJUVANT CHEMOTHERAPY REGIMENS IN OPERABLE OSTEOSARCOMA OF LIMBS IN CHILDREN AND YOUNG-ADULTS - THE 1ST STUDY OF THE EUROPEAN OSTEOSARCOMA INTERGROUP
    BRAMWELL, VHC
    BURGERS, M
    SNEATH, R
    SOUHAMI, R
    VANOOSTEROM, AT
    VOUTE, PA
    ROUESSE, J
    SPOONER, D
    CRAFT, AW
    SOMERS, R
    PRINGLE, J
    MALCOLM, AJ
    VANDEREIJKEN, J
    THOMAS, D
    USCINSKA, B
    MACHIN, D
    VANGLABBEKE, M
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (10) : 1579 - 1591
  • [5] THE ROLE OF CHEMOTHERAPY IN OSTEOGENIC-SARCOMA
    BRAMWELL, VHC
    [J]. CRITICAL REVIEWS IN ONCOLOGY/HEMATOLOGY, 1995, 20 (1-2) : 61 - 85
  • [6] Bramwell VHC, 1997, SEMIN ONCOL, V24, P561
  • [7] CAPANNA R, 1984, CANCER-AM CANCER SOC, V54, P177, DOI 10.1002/1097-0142(19840701)54:1<177::AID-CNCR2820540133>3.0.CO
  • [8] 2-C
  • [9] CARTER SK, 1980, CANCER CLIN TRIALS, V3, P29
  • [10] CHAWLA SP, 1984, ADJUVANT THERAPY CAN, V4, P621