Phase I/II trial of vorinostat with rituximab, cyclophosphamide, etoposide and prednisone as palliative treatment for elderly patients with relapsed or refractory diffuse large B-cell lymphoma not eligible for autologous stem cell transplantation

被引:29
作者
Straus, David J. [1 ]
Hamlin, Paul A. [1 ]
Matasar, Matthew J. [1 ]
Palomba, Maria Lia [1 ]
Drullinsky, Pamela R. [2 ]
Zelenetz, Andrew D. [1 ]
Gerecitano, John F. [1 ]
Noy, Ariela [1 ]
Hamilton, Audrey M. [3 ]
Elstrom, Rebecca [4 ]
Wegner, Brett [1 ]
Wortman, Katy [5 ]
Cella, David [5 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Div Hematol Oncol, Lymphoma Serv, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Rockville Ctr, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Basking Ridge, NJ USA
[4] Weill Cornell Med Coll, Dept Med, Chicago, IL USA
[5] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
vorinostat; combination; relapsed; refractory; elderly; diffuse large B-cell lymphoma; NON-HODGKINS-LYMPHOMA; SUBEROYLANILIDE HYDROXAMIC ACID; HISTONE DEACETYLASE INHIBITORS; CHEMOTHERAPY; GEMCITABINE; COMBINATION; THERAPY; REGIMEN; SAFETY;
D O I
10.1111/bjh.13195
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The standard treatment of relapsed/refractory diffuse large B-cell lymphoma (DLBCL) in frail elderly patients has not been established. A variation was made on rituximab (R), cyclophosphamide (C), etoposide (E), procarbazine and prednisone (P), substituting vorinostat (V) for procarbazine. Patients aged 60years with relapsed/refractory DLBCL, not candidates for autologous stem cell transplantation, were treated R-CVEP [R 375mg/m(2) intravenously (IV), day 1; C 600mg/m(2) IV days 1, 8: E 70mg/m(2) IV day 1, 140mg/m(2) days 2, 3 orally (PO); V (300 vs. 400mg) PO and P 60mg/m(2) PO days 1-10] every 28d for six cycles. Quality of life (QoL) was assessed in addition to response. Thirty patients (median age 76years, 69-88) were enrolled (one died before treatment). Maximum tolerated dose (MTD) for V was 300mg. For 23 patients at MTD (six phase I+17 phase II), two were discontinued for toxicity, one withdrew consent, eight achieved complete response (35%), five achieved partial response (22%) and seven progressed (25%). Median overall survival was 175months. Median progression-free survival was 92months. Nine patients are alive. QoL declined during treatment but improved above baseline for patients who completed treatment. In conclusion, R-CVEP was tolerated at MTD and produced durable responses with improved QoL.
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收藏
页码:663 / 670
页数:8
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