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多中心、随机、双盲、安慰剂对照、探索性研究,评估 HAD-B1 在需要阿法替尼治疗的 EGFR 突变阳性和局部晚期或转移性 NSCLC 受试者中的剂量发现的疗效和安全性。

Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Exploratory Study to Evaluate the Efficacy and Safety of HAD-B1 for Dose-Finding in EGFR Mutation Positive and Locally Advanced or Metastatic NSCLC Subjects Who Need Afatinib Therapy.

机构信息

Daejeon Korean Medicine Hospital of Daejeon University, Daejeon, Republic of Korea.

Seoul Korean Medicine Hospital of Daejeon University, Seoul, Republic of Korea.

出版信息

Integr Cancer Ther. 2021 Jan-Dec;20:15347354211037917. doi: 10.1177/15347354211037917.

Abstract

Afatinib is a target anticancer drug of the second-generation EGFR TKI type, showing an advantage in treatment effect compared to conventional chemotherapy. However, patients on EGFR-TKI drugs also usually progress after 9 to 13 months according to secondary resistance. HAD-B1 is composed of drugs that are effective against lung cancer. This study is an exploratory study to evaluate the efficacy and safety between dosage groups by conducting a clinical trial in subjects requiring afatinib drug treatment in non-small cell lung cancer with EGFR mutation positive to determine the optimal dosage for HAD-B1 administration. At the final visit compared to before administration, each change in the disease control rate was measured according to the HAD-B1 doses of the test group 1 (972 mg), the test group 2 (1944 mg), and the control group. The efficacy and safety of HAD-B1 were compared and evaluated through sub-evaluation variables. As a result of the study, there was no statistically significant difference in the disease control rate at 12 weeks after dosing, but complete and partial remission were evaluated as 1 patient each in the test group 1, and none in the other groups. There was no statistically significant difference between groups in the sub-evaluation variable. In addition, there was no problem of safety from taking the test drug. However, the initially planned number of subjects was 66, but the number of enrolled subjects was only 14, which may limit the results of this study.

摘要

阿法替尼是第二代 EGFR TKI 类的靶向抗癌药物,与传统化疗相比,在治疗效果上具有优势。然而,根据二次耐药性,接受 EGFR-TKI 药物治疗的患者通常在 9 至 13 个月后也会出现进展。HAD-B1 由对肺癌有效的药物组成。本研究是一项探索性研究,通过在需要阿法替尼药物治疗的 EGFR 突变阳性非小细胞肺癌患者中进行临床试验,评估剂量组之间的疗效和安全性,以确定 HAD-B1 给药的最佳剂量。与给药前相比,在最终访视时,根据试验组 1(972mg)、试验组 2(1944mg)和对照组的 HAD-B1 剂量,测量疾病控制率的每个变化。通过子评估变量比较和评估 HAD-B1 的疗效和安全性。研究结果显示,给药后 12 周的疾病控制率没有统计学差异,但在试验组 1 中各有 1 例完全缓解和部分缓解,而其他组均无缓解。组间亚评估变量无统计学差异。此外,服用试验药物没有安全性问题。然而,最初计划的受试者数量为 66 人,但仅招募了 14 人,这可能限制了本研究的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d22b/8381462/e62d066e15a5/10.1177_15347354211037917-fig1.jpg

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