Zaja Francesco, Salvi Flavia, Rossi Maura, Sabattini Elena, Evangelista Andrea, Ciccone Giovannino, Angelucci Emanuele, Gaidano Gianluca, Zanni Manuela, Ladetto Marco, Chiappella Annalisa, Vitolo Umberto, Zinzani Pier Luigi, Califano Catello, Tucci Alessandra, Patti Caterina, Pileri Stefano A, Lenti Valentina, Piccaluga Pier Paolo, Cavallo Federica, Volpetti Stefano, Perali Giulia, Assouline Sarit, Mann Koren Kathleen, Morin Ryan, Alcaide Miguel, Bushell Kevin, Fanin Renato, Levis Alessandro
a Clinica Ematologica ed Unità di Terapie Cellulari 'Carlo Melzi', DAME , University of Udine , Udine , Italy.
b S.C. Ematologia , A.O. SS. Antonio e Biagio e C. Arrigo , Alessandria , Italy.
Leuk Lymphoma. 2018 Dec;59(12):2904-2910. doi: 10.1080/10428194.2018.1452208. Epub 2018 Apr 4.
We investigated panobinostat 40 mg three times weekly in 35 adult patients with relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL). Overall response rate and complete response were 17.1% and 11.4%, respectively. Median progression-free survival (PFS) and overall survival were 2.4 and 7.6 months, respectively. Calculated 12, 24 and 36 months PFS were 26%, 11% and 11%, respectively. Four patients who achieved a sustained CR, continued receiving panobinostat for an overall period of 44, 48, 50, 62 months. Thrombocytopenia grade 3 (5 patients) and 4 (24 patients) represented the main toxic effect, causing dose reduction or treatment suspension in 19 patients. Genomic analysis was unable to identify any relationship between mutations and response; TP53 mutation appeared not to impact the clinical outcome. Overall, panobinostat has a modest activity in R/R DLBCL patients, however it can induce very long lasting responses in some cases. Thrombocytopenia frequently limits the use of this agent.
我们对35例复发/难治性(R/R)弥漫性大B细胞淋巴瘤(DLBCL)成年患者进行了研究,给予其每周3次、每次40毫克的帕比司他治疗。总缓解率和完全缓解率分别为17.1%和11.4%。无进展生存期(PFS)和总生存期的中位数分别为2.4个月和7.6个月。计算得出的12个月、24个月和36个月PFS分别为26%、11%和11%。4例实现持续完全缓解的患者继续接受帕比司他治疗,总疗程分别为44个月、48个月、50个月和62个月。3级血小板减少症(5例)和4级血小板减少症(24例)是主要的毒性反应,导致19例患者出现剂量减少或治疗中断。基因组分析未能确定突变与反应之间的任何关系;TP53突变似乎不影响临床结果。总体而言,帕比司他在R/R DLBCL患者中具有适度的活性,然而在某些情况下它可以诱导非常持久的反应。血小板减少症经常限制该药物的使用。