Concomitant intensive chemoradiotherapy induction in non-metastatic inflammatory breast cancer: long-term follow-up

被引:20
作者
Genet, D.
Lejeune, C.
Bonnier, P.
Aubard, Y.
Venat-Bouvet, L.
Adjadj, D. J.
Martin, J.
Labourey, J. L.
Benyoub, A.
Clavere, P.
Lebrun-Ly, V.
Juin, P.
Piana, L.
Tubiana-Mathieu, N. [1 ]
机构
[1] CHU Dupuytren, Dept Med Oncol, Limoges, France
[2] CHU Conception, Dept Med Oncol, Marseille, France
关键词
inflammatory breast cancer; chemoradiotherapy; breast conservation;
D O I
10.1038/sj.bjc.6603987
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to evaluate with a long follow-up the efficacy of concomitant chemoradiotherapy in non-metastatic inflammatory breast cancer (IBC) and to evaluate the breast conservation rate. Between 1990 and 2000, 66 non-metastatic patients with IBC were treated with chemotherapy and concomitant irradiation. The induction chemotherapy consisted of epirubicine, cyclophosphamide and vindesine, in association with split-course bi-fractionated irradiation to a total dose of 65 Gy with concomitant cisplatin and 5-fluorouracil. Maintenance chemotherapy consisted of high-dose methotrexate and six cycles of epirubicine, cyclophosphamide and fluorouracil. Hormonal treatment was given if indicated. Mastectomy was not systemic. Among 65 evaluable patients, 57 (87.6%) achieved a complete clinical response and had a breast conservation. Only six loco regional relapses were noted in six patients with a delay of 20 months and with concomitant metastatic dissemination in four cases. Median disease-free survival (DFS) was 28 months. Median overall survival (OS) was 63 months and median follow-up was 55.5 months. Induction chemotherapy and concomitant irradiation is feasible in patients with IBC, permitting a breast conservation with a high rate of local control with an OS comparable to that of the best recent series.
引用
收藏
页码:883 / 887
页数:5
相关论文
共 28 条
[1]   Inflammatory breast carcinoma and noninflammatory locally advanced breast carcinoma: Distinct clinicopathologic entities? [J].
Anderson, WF ;
Chu, KC ;
Chang, S .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (12) :2254-2259
[2]   ALTERNATING RADIOTHERAPY AND CHEMOTHERAPY IN NONMETASTATIC INFLAMMATORY BREAST-CANCER [J].
ARRIAGADA, R ;
MOURIESSE, H ;
SPIELMANN, M ;
MEZLINI, A ;
OUDINOT, P ;
LECHEVALIER, T ;
CUVIER, C ;
FONTAINE, F ;
TRAVAGLI, JP ;
MAYLEVIN, F ;
SARRAZIN, D .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1990, 19 (05) :1207-1210
[3]  
Baldini Editta, 2004, Clin Breast Cancer, V5, P358, DOI 10.3816/CBC.2004.n.042
[4]  
BARKER JL, 1980, CANCER, V45, P625, DOI 10.1002/1097-0142(19800215)45:4<625::AID-CNCR2820450402>3.0.CO
[5]  
2-V
[6]   THERAPY FOR INFLAMMATORY BREAST-CANCER - IMPACT OF DOXORUBICIN-BASED THERAPY [J].
BAUER, RL ;
BUSCH, E ;
LEVINE, E ;
EDGE, SB .
ANNALS OF SURGICAL ONCOLOGY, 1995, 2 (04) :288-294
[7]   Inflammatory breast cancer [J].
Cariati, M ;
Bennett-Britton, TM ;
Pinder, SE ;
Purushotham, AD .
SURGICAL ONCOLOGY-OXFORD, 2005, 14 (03) :133-143
[8]  
Chang S, 1998, CANCER, V82, P2366
[9]   THE CENTER-H-BECQUEREL STUDIES IN INFLAMMATORY NONMETASTATIC BREAST-CANCER - COMBINED MODALITY APPROACH IN 178 PATIENTS [J].
CHEVALLIER, B ;
BASTIT, P ;
GRAIC, Y ;
MENARD, JF ;
DAUCE, JP ;
JULIEN, JP ;
CLAVIER, B ;
KUNLIN, A ;
DANJOU, J .
BRITISH JOURNAL OF CANCER, 1993, 67 (03) :594-601
[10]   Update on the management of inflammatory breast cancer [J].
Cristofanilli, M ;
Buzdar, AU ;
Hortobägyi, GN .
ONCOLOGIST, 2003, 8 (02) :141-148