Retrospective Analysis of the Clinical Characteristics of Patients with Breast Cancer Treated with Telomerase Peptide Immunotherapy Combined with Cytotoxic Chemotherapy.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2023-12-21 eCollection Date: 2023-01-01 DOI:10.2147/BCTT.S431333
Jong Yeup Kim, Dong Won Yang, Sangjae Kim, Jong Gwon Choi
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Abstract

Purpose: Telomerase activation, a critical step in cancer progression, occurs in approximately 95% of breast cancer cases. Telomerase is an attractive therapeutic target for breast cancer owing to its unique expression pattern. GV1001, a telomerase-derived peptide, is loaded onto human leukocyte antigen (HLA) class II antigen-presenting cells and binds to CD4+ T cell activating immune responses. This study aimed to evaluate the effectiveness and safety of co-administration of GV1001 and cytotoxic chemotherapy in patients with heavily-treated metastatic breast cancer.

Patients and methods: We analyzed 63 patients with breast cancer who received both GV1001 and cytotoxic chemotherapy. The GV 1001 administration methods involves 0.56 mg intradermal injection three times during the first week, one time at weeks 2, 3, 4, and 6, and then once every 28 days. The primary endpoint of this study was quality of life according to EORTC QLO-C30 and EQ-5D, while the secondary endpoint was the antitumor response according to RECIST 1.1, progression-free survival, overall survival, and toxicity profile.

Results: In 34 patients with HR+ breast cancer evaluable for tumor response, the disease control rate (DCR) and overall response rate (ORR) were 58.8% and 26.4%, respectively. The DCR and ORR were 66.6% and 28.5% in 21 patients with HER-2+ and 50% and 25% in patients with triple-negative breast cancer (TNBC), respectively. The median progression free survival was 10.4, 8.7, and 5.6 months in HR+, HER-2+, TNBC, respectively. The overall survival was 19.7, 13.2, and 9.4 months for patients with HR+, HER-2+, and TNBC, respectively. Most patients had an improved quality of life with statistically significant differences in some variables. The patients in this study experienced no additional toxicities other than the cytotoxic chemotherapy-associated side effects.

Conclusion: GV1001 is a relatively safe anticancer vaccine for patients with heavily-treated breast cancer and can to improve the quality of life.

端粒酶肽免疫疗法联合细胞毒化疗治疗乳腺癌患者临床特征的回顾性分析
目的:端粒酶激活是癌症进展的关键步骤,大约 95% 的乳腺癌病例都会发生端粒酶激活。端粒酶因其独特的表达模式而成为乳腺癌的治疗靶点。GV1001是一种端粒酶衍生的多肽,被载入人类白细胞抗原(HLA)II类抗原递呈细胞,并与CD4+ T细胞结合,激活免疫反应。本研究旨在评估在重度转移性乳腺癌患者中联合应用 GV1001 和细胞毒化疗的有效性和安全性:我们分析了63名同时接受GV1001和细胞毒化疗的乳腺癌患者。GV 1001 的给药方法是在第一周皮内注射 3 次 0.56 毫克,第 2、3、4 和 6 周各注射 1 次,然后每 28 天注射 1 次。这项研究的主要终点是根据 EORTC QLO-C30 和 EQ-5D 评定的生活质量,次要终点是根据 RECIST 1.1 评定的抗肿瘤反应、无进展生存期、总生存期和毒性概况:在34例可评估肿瘤反应的HR+乳腺癌患者中,疾病控制率(DCR)和总反应率(ORR)分别为58.8%和26.4%。21例HER-2+患者的疾病控制率和总反应率分别为66.6%和28.5%,三阴性乳腺癌(TNBC)患者的疾病控制率和总反应率分别为50%和25%。HR+、HER-2+和TNBC患者的中位无进展生存期分别为10.4、8.7和5.6个月。HR+、HER-2+和TNBC患者的总生存期分别为19.7、13.2和9.4个月。大多数患者的生活质量都有所改善,某些变量的差异具有统计学意义。除细胞毒性化疗相关副作用外,本研究中的患者没有出现其他毒性反应:结论:GV1001 是一种相对安全的抗癌疫苗,适用于重症乳腺癌患者,并能改善患者的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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