Portell Craig A, Jegede Opeyemi A, Wagner-Johnston Nina, Nowakowski Grzegorz S, Fletcher Christopher, Cohen Jonathon B, Evens Andrew M, Rosenstein Lori J, Craig Jeffrey W, Reddy Nishitha, Kahl Brad S
University of Virginia Comprehensive Cancer Center, Charlottesville, VA, USA.
Dana-Farber Cancer Institute, Boston, MA, USA.
Blood Cancer J. 2025 May 12;15(1):93. doi: 10.1038/s41408-025-01300-1.
Over-expression of BCL-2 defines follicular lymphoma (FL). Venetoclax (VEN), a selective BCL-2 inhibitor, has previously been evaluated with bendamustine-based chemoimmunotherapy. VEN was given continuously, resulting in promising efficacy but unacceptable toxicity. The Phase II PrE0403 study was designed to evaluate intermittent dosing of VEN (10 days per cycle) combined with obinutuzumab and bendamustine (VEN-OB) in untreated FL subjects with high-risk features defined as a FLIPI-1 score of ≥3 and/or high tumor burden by GELF criteria. A total of 56 subjects were planned to be accrued with a goal of having 51 subjects eligible to improve the historical 50% CR rate to 65% with an 85% power and 15% type I error rate. Immunohistochemistry (IHC) expression of 3 antiapoptotic proteins (BCL-xL, MCL-1, and BCL-2) was performed and correlated with clinical outcomes. All 56 subjects were eligible and treated. CR rate was 41/56 (73.2%) and ORR was 52/56 (92.5%) meeting the primary endpoint. 2-year estimated PFS was 87.5% (90% CI: 75.3,93.9%) and 2-year estimated OS was 94.6% (90% CI: 86.7, 97.9%). However, the incidence of treatment-related adverse events ≥ grade 3 was 83.9% and serious adverse events were seen in 57.1%. After induction, atypical infections, including Grade 5 events, occurred. Anti-apoptotic protein expression by IHC was not correlated with clinical outcomes. Thus, while meeting the primary efficacy end point, VEN-OB is considered overly toxic in high-risk FL.
BCL-2的过表达可定义滤泡性淋巴瘤(FL)。维奈克拉(VEN)是一种选择性BCL-2抑制剂,此前已与基于苯达莫司汀的化疗免疫疗法联合进行评估。VEN持续给药,疗效显著,但毒性难以接受。II期PrE0403研究旨在评估VEN间歇给药(每周期10天)联合奥妥珠单抗和苯达莫司汀(VEN-OB)用于治疗具有高危特征的初治FL患者,高危特征定义为FLIPI-1评分≥3和/或根据GELF标准肿瘤负荷高。计划共纳入56例受试者,目标是使51例受试者符合条件,将历史50%的完全缓解(CR)率提高到65%,检验效能为85%,I类错误率为15%。进行了3种抗凋亡蛋白(BCL-xL、MCL-1和BCL-2)的免疫组织化学(IHC)表达检测,并将其与临床结果相关联。所有56例受试者均符合条件并接受了治疗。CR率为41/56(73.2%),总缓解率(ORR)为52/56(92.5%),达到了主要终点。2年预估无进展生存期(PFS)为87.5%(90%CI:75.3,93.9%),2年预估总生存期(OS)为94.6%(90%CI:86.7,97.9%)。然而,≥3级治疗相关不良事件的发生率为83.9%,严重不良事件的发生率为57.1%。诱导治疗后,发生了包括5级事件在内的非典型感染。IHC检测的抗凋亡蛋白表达与临床结果无关。因此,虽然达到了主要疗效终点,但VEN-OB在高危FL中被认为毒性过大。