Department of Clinical Medicine and Surgery, Federico II University Medical School, Naples, Italy.
Department of Public Health, Federico II University Medical School, Naples, Italy.
Br J Haematol. 2022 Sep;198(5):847-860. doi: 10.1111/bjh.18348. Epub 2022 Jul 12.
We evaluated the impact of liposomal doxorubicin (NPLD) supercharge-containing therapy on interim fluorodeoxyglucose positron emission tomography (interim-FDG-PET) responses in high-risk diffuse large B-cell lymphoma (DLBCL) or classical Hodgkin lymphoma (c-HL). In this phase II study (2016-2021), 81 adult patients with advanced-stage DLBCL (n = 53) and c-HL (n = 28) received front-line treatment with R-COMP-dose-intensified (DI) and MBVD-DI. R-COMP-DI consisted of 70 mg/m of NPLD plus standard rituximab, cyclophosphamide, vincristine and prednisone for three cycles (followed by three cycles with NPLD de-escalated at 50 mg/m ); MBVD-DI consisted of 35 mg/m of NPLD plus standard bleomycin, vinblastine and dacarbazine for two cycles (followed by four cycles with NPLD de-escalated at 25 mg/m ). Patients underwent R-COMP-DI and MBVD-DI with a median dose intensity of 91% and 94% respectively. At interim-FDG-PET, 72/81 patients (one failed to undergo interim-FDG-PET due to early death) had a Deauville score of ≤3. At end of treatment, 90% of patients reached complete responses. In all, 20 patients had Grade ≥3 adverse events, and four of them required hospitalisation. At a median 21-months of follow-up, the progression-free survival of the entire population was 77.3% (95% confidence interval 68%-88%). Our data suggest that the NPLD supercharge-driven strategy in high-risk DLBCL/c-HL may be a promising option to test in phase III trials, for improving negative interim-FDG-PET cases incidence.
我们评估了脂质体多柔比星(NPLD)强化治疗对高危弥漫性大 B 细胞淋巴瘤(DLBCL)或经典霍奇金淋巴瘤(cHL)患者中间氟脱氧葡萄糖正电子发射断层扫描(interim-FDG-PET)反应的影响。在这项 2 期研究(2016-2021 年)中,81 名晚期 DLBCL(n=53)和 cHL(n=28)成年患者接受了一线 R-COMP-剂量强化(DI)和 MBVD-DI 治疗。R-COMP-DI 由 70mg/m 的 NPLD 加标准利妥昔单抗、环磷酰胺、长春新碱和泼尼松组成,共 3 个周期(随后是 3 个周期,NPLD 剂量降低至 50mg/m);MBVD-DI 由 35mg/m 的 NPLD 加标准博来霉素、长春碱和达卡巴嗪组成,共 2 个周期(随后是 4 个周期,NPLD 剂量降低至 25mg/m)。患者接受了中位剂量强度分别为 91%和 94%的 R-COMP-DI 和 MBVD-DI 治疗。在中间-FDG-PET 时,81 例患者中有 72 例(由于早期死亡,1 例未能进行中间-FDG-PET)的 Deauville 评分≤3。在治疗结束时,90%的患者达到完全缓解。共有 20 例患者发生≥3 级不良事件,其中 4 例需要住院治疗。在中位随访 21 个月时,整个人群的无进展生存率为 77.3%(95%置信区间为 68%-88%)。我们的数据表明,高危 DLBCL/cHL 中 NPLD 强化驱动的策略可能是在 3 期试验中进行测试的一个有前途的选择,以提高阴性中间-FDG-PET 病例的发生率。