Moffitt Cancer Center, Tampa, FL, USA.
Cancer. 2013 Mar 1;119(5):1023-32. doi: 10.1002/cncr.27836. Epub 2012 Oct 12.
Chemoprevention for lung cancer with nutraceutical or anti-inflammatory agents has had mixed clinical benefit. Novel targeted agents hold the promise of greater efficacy and selectivity. The authors of this report evaluated enzastaurin, a selective protein kinase C-β (PKC-β) inhibitor with antiproliferative and proapoptotic properties, in former smokers.
The primary objective of this study was to compare the average fraction of Ki-67-stained cells (the Ki-67 labeling index [LI]) in bronchial biopsy specimens that were collected before and after treatment. Participants were randomized (2:1) to receive either 6 months of daily oral enzastaurin (500 mg) or placebo. Stratification was based on morphology, history of lung cancer, and airway obstruction.
In pretrial investigations, the rationale for PKC-β inhibition and pathway interrogation was established in premalignant lesions and early stage lung cancer. In an intent-to-treat analysis, of 40 randomized participants, there was no significant difference in the pretreatment/post-treatment change in the Ki-67 LI between the enzastaurin group and the placebo group (P = .53). Six participants discontinued enzastaurin, including 4 participants who had adverse events, including abdominal distension, deep vein thrombosis, hyponatremia, and rash, and 2 participants who decided to discontinue. One participant in the placebo group was discontinued on the study because of noncompliance. Two participants had ≥1 serious adverse event (bradycardia, deep vein thrombosis, and hypotension).
To the authors' knowledge, this represents the first chemoprevention trial with a non-US Food and Drug Administration-approved, oral, small-molecule-targeted agent. Although the primary endpoint was not met, enzastaurin was tolerable for 6 months by 75% of participants, and there was a suggestion of response in a subset analysis that was restricted to those who had metaplastic or dysplastic lesions.
用营养保健品或抗炎药物进行肺癌化学预防的临床获益参差不齐。新型靶向药物有望具有更高的疗效和选择性。本文作者评估了前吸烟者使用恩杂鲁胺(一种具有抗增殖和促凋亡作用的选择性蛋白激酶 C-β(PKC-β)抑制剂)的情况。
本研究的主要目的是比较治疗前后支气管活检标本中 Ki-67 染色细胞(Ki-67 标记指数[LI])的平均分数。参与者被随机(2:1)分配接受 6 个月的每日口服恩杂鲁胺(500mg)或安慰剂。分层基于形态学、肺癌病史和气道阻塞。
在预试验研究中,在癌前病变和早期肺癌中确立了 PKC-β 抑制和通路检测的原理。在意向治疗分析中,在 40 名随机参与者中,恩杂鲁胺组和安慰剂组之间 Ki-67 LI 的预处理/后处理变化无显著差异(P=.53)。6 名参与者停止服用恩杂鲁胺,包括 4 名因腹部膨胀、深静脉血栓形成、低钠血症和皮疹等不良反应而停药的参与者,以及 2 名决定停药的参与者。安慰剂组中有 1 名参与者因不遵从而被终止研究。2 名参与者发生≥1 例严重不良事件(心动过缓、深静脉血栓形成和低血压)。
据作者所知,这是首个使用非美国食品和药物管理局批准的口服小分子靶向药物进行化学预防的试验。尽管主要终点未达到,但 75%的参与者可耐受恩杂鲁胺 6 个月,并且在仅限于具有化生或发育不良病变的亚组分析中提示有反应。