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三期临床试验研究替比嘧啶软膏治疗光化性角化病。

Phase 3 Trials of Tirbanibulin Ointment for Actinic Keratosis.

机构信息

From the Oregon Medical Research Center, Portland (A.B.); the Minnesota Clinical Study Center, New Brighton (S.K.); the Austin Institute for Clinical Research, Pflugerville (E.L.), and the Department of Dermatology and Center for Clinical Studies, University of Texas Health Science Center at Houston, Houston (S.T.) - both in Texas; the Clinical Research Center of the Carolinas, Charleston, SC (T.S.); ForCare Clinical Research, Tampa, FL (S.F.); Ablon Skin Institute Research Center, Manhattan Beach, CA (G.A.); Dr. George Martin Dermatology Associates, Kihei, HI (G.M.); and Athenex, Buffalo, NY (H.W., D.L.C., J.F., M.-F.R.K.).

出版信息

N Engl J Med. 2021 Feb 11;384(6):512-520. doi: 10.1056/NEJMoa2024040.

Abstract

BACKGROUND

The tubulin polymerization and Src kinase signaling inhibitor tirbanibulin is being investigated as a topical treatment for actinic keratosis, a precursor of squamous-cell carcinoma.

METHODS

In two identically designed double-blind trials, we randomly assigned, in a 1:1 ratio, adults with actinic keratoses on the face or scalp to receive either topical tirbanibulin or vehicle (placebo) ointment. The ointment was applied by the patients to a 25-cm contiguous area containing four to eight lesions once daily for 5 consecutive days. The primary outcome was the percentage of patients with a complete (100%) reduction in the number of lesions in the application area at day 57. The secondary outcome was the percentage of patients with a partial (≥75%) reduction in the number of lesions within the application area at day 57. The incidence of recurrence was evaluated at 1 year. Local reactions were scored with the use of 4-point scale (ranging from 0 [absent] to 3 [severe]).

RESULTS

A total of 702 patients were enrolled in the two trials (351 patients per trial). Complete clearance in trial 1 occurred in 44% of the patients (77 of 175) in the tirbanibulin group and in 5% of those (8 of 176) in the vehicle group (difference, 40 percentage points; 95% confidence interval [CI], 32 to 47; P<0.001); in trial 2, the percentages were 54% (97 of 178 patients) and 13% (22 of 173), respectively (difference, 42 percentage points; 95% CI, 33 to 51; P<0.001). The percentages of patients with partial clearance were significantly higher in the tirbanibulin groups than in the vehicle groups. At 1 year, the estimated percentage of patients with recurrent lesions was 47% among patients who had had a complete response to tirbanibulin. The most common local reactions to tirbanibulin were erythema in 91% of the patients and flaking or scaling in 82%. Adverse events with tirbanibulin were application-site pain in 10% of the patients and pruritus in 9%, all of which resolved.

CONCLUSIONS

In two identically designed trials, tirbanibulin 1% ointment applied once daily for 5 days was superior to vehicle for the treatment of actinic keratosis at 2 months but was associated with transient local reactions and recurrence of lesions at 1 year. Trials comparing tirbanibulin with conventional treatments and that have longer follow-up are needed to determine the effects of tirbanibulin therapy on actinic keratosis. (Funded by Athenex; ClinicalTrials.gov numbers, NCT03285477 and NCT03285490.).

摘要

背景

微管聚合和Src 激酶信号抑制剂替拉那布林正在被研究作为一种治疗光化性角化病(鳞状细胞癌的前身)的局部治疗药物。

方法

在两项设计相同的双盲试验中,我们以 1:1 的比例随机分配面部或头皮上患有光化性角化病的成年人接受替拉那布林或安慰剂(载体)软膏治疗。患者每天将软膏涂于包含四到八个病变的 25cm 连续区域,连续 5 天,每天一次。主要终点是在第 57 天应用区域内病变数量完全(100%)减少的患者百分比。次要终点是在第 57 天应用区域内病变数量部分(≥75%)减少的患者百分比。在 1 年时评估复发情况。使用 4 分制(范围为 0[不存在]至 3[严重])对局部反应进行评分。

结果

两项试验共纳入 702 名患者(每项试验 351 名患者)。在试验 1 中,替拉那布林组有 44%(175 名患者中的 77 名)完全清除,而安慰剂组只有 5%(176 名患者中的 8 名)(差异为 40 个百分点;95%置信区间[CI],32 至 47;P<0.001);在试验 2 中,相应的百分比分别为 54%(178 名患者中的 97 名)和 13%(173 名患者中的 22 名)(差异为 42 个百分点;95%CI,33 至 51;P<0.001)。替拉那布林组的患者完全清除率明显高于安慰剂组。在 1 年时,对替拉那布林有完全反应的患者中,估计有 47%的患者出现复发性病变。替拉那布林最常见的局部反应是 91%的患者出现红斑和 82%的患者出现脱屑或鳞屑。替拉那布林相关的不良事件为 10%的患者出现用药部位疼痛和 9%的患者出现瘙痒,均已缓解。

结论

在两项设计相同的试验中,替拉那布林 1%软膏每天应用 5 天,在治疗 2 个月时优于安慰剂,但与短暂的局部反应和 1 年时的病变复发有关。需要比较替拉那布林与传统治疗方法的临床试验,并进行更长时间的随访,以确定替拉那布林治疗对光化性角化病的影响。(由 Athenex 资助;临床试验.gov 编号,NCT03285477 和 NCT03285490)。

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