Neoadjuvant chemotherapy for extremity osteosarcoma -: Preliminary results of the Rizzoli's 4th study

被引:71
作者
Bacci, G
Ferrari, S
Mercuri, M
Longhi, A
Capanna, R
Tienghi, A
del Prever, AB
Comandone, A
Cesari, M
Bernini, G
Picci, P
机构
[1] Ist Ortoped Rizzoli, Dept Chemotherapy, I-40136 Bologna, Italy
[2] Ist Ortoped Rizzoli, Dept Orthopaed Surg 5, I-40136 Bologna, Italy
[3] Ist Ortoped Rizzoli, Lab Oncol Res, I-40136 Bologna, Italy
[4] CTO, Dept Orthopaed Oncol & Reconstruct Surg, Firenze, Italy
[5] Osped Santa Croce, Dept Med Oncol, Ravenna, Italy
[6] Univ Turin, Pediat Clin, Torino, Italy
[7] Osped Giovanni Vecchio, Dept Med Oncol, Torino, Italy
[8] Ist Mayer Firenze, Unit Pediat Oncohematol, Firenze, Italy
关键词
D O I
10.1080/028418698423168
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A neoadjuvant chemotherapy protocol (1/93-1/95) for extremity osteosarcoma preoperatively using high-dose methotrexate (HDMTX) as single agent per cycle and three different combinations of other drugs (CDP/IFO,CDP/ADM,IFO/ADM) is reported. The four drugs were used postoperatively as single agents. Treatment was uniform, but suspended earlier if total necrosis was attained. An improvement was found in the results of the previous study using only IFO postoperatively, with 16/119 patients (97%) avoiding amputation, and 38 (32%) attaining complete necrosis. At a 3-year (2-4 years) mean follow-up, 92 patients (76%) remained continuously disease-free. 2 died of chemotherapy-related toxicity and 25 suffered relapse. Projected 3-year DFS also improved (75% vs. 60%; p = 0.04). Despite limb salvage, local recurrences (6.3%) and infections were few, although postoperative chemotherapy was restarted within a week. Therefore, until new effective drugs are found, expertise in using the four known drugs may improve cure rate and help to avoid amputation in almost all patients.
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页码:41 / 48
页数:8
相关论文
共 23 条
[1]  
BACCI G, 1993, J CHEMOTHERAPY, V5, P237
[2]  
BACCI G, 1993, CANCER, V72, P3227, DOI 10.1002/1097-0142(19931201)72:11<3227::AID-CNCR2820721116>3.0.CO
[3]  
2-C
[4]  
BACCI G, 1990, CANCER, V65, P2539, DOI 10.1002/1097-0142(19900601)65:11<2539::AID-CNCR2820651125>3.0.CO
[5]  
2-M
[6]  
BENJAMIN R S, 1988, P269
[7]  
BENJAMIN RS, 1993, CANCER CHEMOTHER PHA, V31, P174
[8]  
BOWMAN LC, 1987, P AN M AM SOC CLIN, V6, P214
[9]   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 [J].
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 .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (10) :1579-1591
[10]  
DELEPINE G, 1986, REV RHUM, V53, P539