University of Wisconsin Paul P. Carbone Cancer Center, Madison, USA.
Cancer Prev Res (Phila). 2010 Jan;3(1):35-47. doi: 10.1158/1940-6207.CAPR-09-0096.
Preclinical studies have shown that the inhibition of ornithine decarboxylase (ODC) by alpha-difluoromethylornithine (DFMO) and resultant decreases in tissue concentrations of polyamines (putrescine and spermidine) prevents neoplastic developments in many tissue types. Clinical studies of oral DFMO at 500 mg/m(2)/day revealed it to be safe and tolerable and resulted in significant inhibition of phorbol ester-induced skin ODC activity. Two hundred and ninety-one participants (mean age, 61 years; 60% male) with a history of prior nonmelanoma skin cancer (NMSC; mean, 4.5 skin cancers) were randomized to oral DFMO (500 mg/m(2)/day) or placebo for 4 to 5 years. There was a trend toward a history of more prior skin cancers in subjects randomized to placebo, but all other characteristics including sunscreen and nonsteroidal anti-inflammatory drug use were evenly distributed. Evaluation of 1,200 person-years of follow-up revealed a new NMSC rate of 0.5 events/person/year. The primary end point, new NMSCs, was not significantly different between subjects taking DFMO and placebo (260 versus 363 cancers, P = 0.069, two-sample t test). Evaluation of basal cell (BCC) and squamous cell cancers separately revealed very little difference in squamous cell cancer between treatment groups but a significant difference in new BCC (DFMO, 163 cancers; placebo, 243 cancers; expressed as event rate of 0.28 BCC/person/year versus 0.40 BCC/person/year, P = 0.03). Compliance with DFMO was >90% and it seemed to be well tolerated with evidence of mild ototoxicity as measured by serial audiometric examination when compared with placebo subjects. The analysis of normal skin biopsies revealed a significant (P < 0.05) decrease in 12-0-tetradecanoylphorbol-13-acetate-induced ODC activity (month 24, 36, and 48) and putrescine concentration (month 24 and 36 only) in DFMO subjects. Subjects with a history of skin cancer taking daily DFMO had an insignificant reduction (P = 0.069) in new NMSC that was predominantly due to a marked reduction in new BCC. Based on these data, the potential of DFMO, alone or in combination, to prevent skin cancers should be explored further.
临床前研究表明,通过 α-二氟甲基鸟氨酸(DFMO)抑制鸟氨酸脱羧酶(ODC),导致组织中多胺(腐胺和精胺)浓度降低,可以预防许多组织类型的肿瘤发生。口服 DFMO(500mg/m²/天)的临床研究表明其安全且可耐受,并可显著抑制佛波酯诱导的皮肤 ODC 活性。291 名参与者(平均年龄 61 岁;60%为男性)有非黑色素瘤皮肤癌(NMSC)既往史(平均 4.5 个皮肤癌),随机接受口服 DFMO(500mg/m²/天)或安慰剂治疗 4 至 5 年。随机接受安慰剂治疗的患者既往皮肤癌病史呈增加趋势,但所有其他特征,包括防晒霜和非甾体抗炎药的使用,分布均匀。1200 人年的随访评估显示,新发 NMSC 发生率为 0.5 例/人/年。主要终点,新发 NMSC,DFMO 组与安慰剂组无显著差异(260 例与 363 例癌症,P=0.069,两样本 t 检验)。分别评估基底细胞癌(BCC)和鳞状细胞癌,发现两组间鳞状细胞癌差异甚微,但新 BCC 差异显著(DFMO 组 163 例;安慰剂组 243 例;BCC 发生率分别为 0.28 例/人/年和 0.40 例/人/年,P=0.03)。DFMO 的依从性>90%,与安慰剂组相比,连续听力学检查显示出轻微的耳毒性,耐受性似乎较好。对正常皮肤活检的分析显示,DFMO 组 12-氧十四烷酰佛波醇-13-乙酸(12-O-tetradecanoylphorbol-13-acetate,TPA)诱导的 ODC 活性(第 24、36 和 48 个月)和腐胺浓度(仅第 24 和 36 个月)显著降低(P<0.05)。有皮肤癌既往史的患者每日服用 DFMO,新发 NMSC 减少不显著(P=0.069),主要是由于新发 BCC 明显减少。基于这些数据,DFMO 单独或联合应用预防皮肤癌的潜力应进一步探索。