Division of Hematology/Oncology, Tufts University School of Medicine, Boston, MA, USA.
Br J Haematol. 2013 Oct;163(1):55-61. doi: 10.1111/bjh.12488. Epub 2013 Aug 8.
There remains an unmet therapeutic need for patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL) and peripheral T-cell lymphoma (PTCL). We conducted a phase I/II trial with bortezomib (dose-escalated to 1·6 mg/m(2) ) given concurrently with gemcitabine (800 mg/m(2) ) days 1 + 8 q21 d. Of 32 patients, 16 each had relapsed/refractory PTCL and DLBCL. Median prior therapies were 3 and 35% had failed transplant. Among the first 18 patients, 67% experienced grade 3/4 neutropenia and/or grade 3/4 thrombocytopenia resulting in repeated treatment delays (relative dose intensity: 46%). Thus, the study was amended to give bortezomib and gemcitabine days 1 + 15 q28 d, which resulted in markedly improved tolerability. Among all patients, the overall response rate (ORR) was 24% with 19% complete remission (CR; intent-to-treat (ITT) ORR 16%, CR 13%), which met criteria for futility. The ORR for DLBCL was 10% (CR 10%) vs. 36% for PTCL (CR 27%). Among 6 PTCL patients treated on the modified schedule, ORR by ITT was 50% (CR 30%). Altogether, concurrent bortezomib/gemcitabine given days 1 + 8 q21 d was not tolerable, while modification to a bi-monthly schedule allowed consistent treatment delivery. Whereas efficacy of this combination was low in heavily pre-treated DLBCL, there was a signal of activity in relapsed/refractory PTCL utilizing the modified schedule.
对于复发/难治性弥漫性大 B 细胞淋巴瘤(DLBCL)和外周 T 细胞淋巴瘤(PTCL)患者,仍存在未满足的治疗需求。我们进行了一项硼替佐米(剂量递增至 1.6mg/m2)与吉西他滨(800mg/m2)联合用药的 I/II 期试验,第 1 天和第 8 天给药,q21d。32 例患者中,16 例分别患有复发/难治性 PTCL 和 DLBCL。中位既往治疗数为 3 次,35%的患者移植后复发。在前 18 例患者中,67%的患者发生 3/4 级中性粒细胞减少和/或 3/4 级血小板减少,导致治疗反复延迟(相对剂量强度:46%)。因此,研究方案修改为第 1 天和第 15 天给药,q28d,这显著改善了耐受性。在所有患者中,总体缓解率(ORR)为 24%,完全缓解率(CR)为 19%(意向治疗(ITT)ORR 为 16%,CR 为 13%),达到了无效标准。DLBCL 的 ORR 为 10%(CR 为 10%),而 PTCL 的 ORR 为 36%(CR 为 27%)。在按修改方案治疗的 6 例 PTCL 患者中,ITT 的 ORR 为 50%(CR 为 30%)。总之,第 1 天和第 8 天给药,q21d 的硼替佐米/吉西他滨方案不耐受,而修改为每 2 个月给药的方案可以保证持续治疗。尽管该联合方案在经大量预处理的 DLBCL 中的疗效较低,但在使用修改方案时,复发/难治性 PTCL 显示出活性信号。