A phase II study of alemtuzumab, fludarabine, cyclophosphamide, and doxorubicin (Campath-FCD) in peripheral T-cell lymphomas

被引:22
作者
Weidmann, Eckhart [1 ]
Hess, Georg [2 ]
Chow, Kai U. [3 ]
Krause, Stefan W. [4 ]
Subklewe, Marion [5 ]
Kruse, Judith [1 ]
Weisel, Katja C. [6 ]
Soekler, Martin [6 ]
Kim, Soo-Zin [7 ]
Napieralski, Simone [10 ]
Rech, Juergen [8 ,9 ]
Dreyling, Martin [11 ]
Jaeger, Elke [1 ]
Mitrou, Paris S. [7 ]
机构
[1] Krankenhaus NW Frankfurt, Klin Onkol & Hamatol, D-60488 Frankfurt, Germany
[2] Johannes Gutenberg Univ Mainz, Dept Hematol Oncol, Mainz, Germany
[3] Med Practice Ctr, Frankfurt, Germany
[4] Univ Hosp Regensburg, Dept Hematol Oncol, Regensburg, Germany
[5] Charite, Med Klin MS Hamatol Onkol, D-13353 Berlin, Germany
[6] Univ Tubingen, Med Ctr, Dept Hematol Oncol & Immunol, Tubingen, Germany
[7] Goethe Univ Frankfurt, Dept Internal Med 2, Frankfurt, Germany
[8] Univ Erlangen Nurnberg, Med Clin 3, D-8520 Erlangen, Germany
[9] Univ Erlangen Nurnberg, Dept Clin Immunol, D-8520 Erlangen, Germany
[10] Univ Marburg, Klin Hamatol Onkol & Immunol, Marburg, Germany
[11] Univ Munich, Dept Internal Med 3, Grosshadern Hosp, Munich, Germany
关键词
Alemtuzumab; fludarabine; peripheral T-cell lymphoma (PTCL); ANTI-CD52; MONOCLONAL-ANTIBODY; CHRONIC LYMPHOCYTIC-LEUKEMIA; CARDIAC TOXICITY; CHEMOTHERAPY; COMBINATION; THERAPY; CHOP; GUIDELINES; MANAGEMENT; EXPRESSION;
D O I
10.3109/10428190903580402
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The clinical course of peripheral T-cell lymphoma (PTCL) is usually aggressive and the prognosis unfavorable. Therefore, there is a need for improvement of treatment options. Patients with newly diagnosed (n = 27) or refractory/relapsed (n = 11) PTCL received a combination of alemtuzumab, fludarabine, cyclophosphamide, and doxorubicin. The overall response rate (ORR) was 61%, with a complete response rate of 39%. In newly diagnosed patients the ORR was 63%, the median overall survival 25.9 months, and progression-free survival 11.8 months. In relapsed/refractory patients the median OS was 6.1 months. The most frequent grade 3/4 toxicities were leukopenia (95% of patients) and thrombocytopenia (58%). Cytomegalovirus (CMV) reactivation occurred in 12 patients, but only two had CMV disease. Treatment-related deaths occurred in six newly diagnosed patients and one with relapsed/refractory disease. In conclusion, Campath-FCD is active in PTCL but is associated with significant toxicity and is, therefore, not recommended for use or further study. Further studies are warranted to investigate other approaches to combining alemtuzumab with chemotherapy for the treatment of PTCL.</.
引用
收藏
页码:447 / 455
页数:9
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