Panobinostat in Patients With Relapsed/Refractory Hodgkin's Lymphoma After Autologous Stem-Cell Transplantation: Results of a Phase II Study

被引:197
|
作者
Younes, Anas [1 ]
Sureda, Anna [2 ]
Ben-Yehuda, Dina [3 ]
Zinzani, Pier Luigi [4 ]
Ong, Tee-Chuan [5 ]
Prince, H. Miles [6 ,7 ]
Harrison, Simon J. [6 ,7 ]
Kirschbaum, Mark [8 ]
Johnston, Patrick [9 ]
Gallagher, Jennifer [10 ]
Le Corre, Christophe [10 ]
Shen, Angela [10 ]
Engert, Andreas [11 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Unite 429, Houston, TX 77030 USA
[2] Hosp Santa Creu & Sant Pau, Barcelona, Spain
[3] Hadassah Med Org, Jerusalem, Israel
[4] Univ Bologna, Inst Hematol & Med Oncol L&A Seragnoli, Bologna, Italy
[5] Hosp Ampang, Ampang, Selangor, Malaysia
[6] Univ Melbourne, Melbourne, Vic, Australia
[7] Peter MacCallum Canc Ctr, Melbourne, Vic, Australia
[8] City Hope Natl Med Ctr, Duarte, CA 91010 USA
[9] Mayo Clin, Rochester, MN USA
[10] Novartis Pharmaceut, Florham Pk, NJ USA
[11] Klinikum Univ Koln, Cologne, Germany
关键词
HISTONE DEACETYLASE INHIBITORS; RESPONSE CRITERIA; RANDOMIZED-TRIAL; DISEASE; LBH589; CHEMOKINE; THERAPY;
D O I
10.1200/JCO.2011.38.1350
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Hodgkin's lymphoma (HL) has no standard of care for patients who are relapsed or refractory to autologous stem-cell transplantation (ASCT). This phase II study examined safety and activity of panobinostat in this population. Patients and Methods Panobinostat 40 mg was administered orally three times per week. The primary end point was objective response rate (ORR) based on investigator assessment of radiologic imaging. Secondary end points included ORR by independent central review, time to response (TTR), duration of response (DOR), progression-free survival (PFS), overall survival, and safety. Exploratory biomarker analyses were performed. Results The 129 treated patients (median age, 32 years; range, 18 to 75 years) were heavily pretreated with a median of four (range, two to seven) prior systemic regimens, and 41% did not respond to the regimen immediately preceding panobinostat. Tumor reductions occurred in 96 patients (74%). Objective response was achieved by 35 patients (27%), including 30 (23%) partial responses and five (4%) complete responses. The median TTR was 2.3 months, median DOR was 6.9 months, and median PFS was 6.1 months. The estimated 1-year overall survival rate was 78%. Common nonhematologic adverse events (AEs)-diarrhea, nausea, vomiting, and fatigue-were generally grade 1 and 2. Most common grade 3 and 4 hematologic AEs-thrombocytopenia, anemia, and neutropenia-were manageable. Early reductions in thymus and activation-regulated chemokine were observed in patients achieving complete or partial response. Conclusion In the largest, prospective, multicenter, international trial conducted in heavily pretreated patients with HL who relapsed or were refractory to ASCT, panobinostat monotherapy demonstrated antitumor activity, resulting in durable responses. J Clin Oncol 30:2197-2203. (c) 2012 by American Society of Clinical Oncology
引用
收藏
页码:2197 / 2203
页数:7
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