[pertuzumab(基因重组)、曲妥珠单抗(基因重组)和 vorhyaluronidase alfa(基因重组)(PHESGO® 组合,用于‍皮下注射 MA、IN)的药理特性和临床开发概述]。

Mariko Sakaeda, Naoki Kotani, Takaaki Yoneya, Yue Zheng, Yuji Habara
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引用次数: 0

摘要

帕妥珠单抗和曲妥珠单抗是抗 HER2 的人源化单克隆抗体,具有不同的作用机制。它们的联合用药有望以叠加或协同的方式抑制细胞内的 HER2 信号传导。它们的联合用药在全球得到广泛推荐,并已被确立为治疗 HER2 阳性乳腺癌的标准疗法。然而,由于静脉输注时间较长,因此还需要改进。vorhyaluronidase alfa(rHuPH20)可分解皮下结缔组织中的透明质酸。据报道,它能提高药物的渗透性和吸收水平。用于皮下注射的 PHESGO® MA/IN 复方制剂(PHESGO®)是一种由百妥珠单抗、曲妥珠单抗和 rHuPH20 组成的固定剂量复方制剂。在I期剂量摸底研究(BO30185)之后进行了III期确证研究(FeDeriCa)。HER2阳性早期乳腺癌患者被随机分配接受静脉输注pertuzumab和曲妥珠单抗或皮下注射PHESGO®,并与化疗联合使用,以比较药代动力学(PK)、疗效和安全性。此外,还进行了一项II期研究(PHranceSCa),以评估患者的偏好和满意度。基于这些结果、群体 PK 分析和其他数据,PHESGO® 于 2023 年 9 月在日本获得上市许可,适应症为 "HER2 阳性乳腺癌 "和 "晚期或复发性 HER2 阳性结直肠癌,且在癌症化疗后病情进展,无法进行根治性切除"。通过缩短给药时间,PHESGO®有望满足患者的各种需求,改善他们的日常生活。由于不需要配制药物,它可以为医护人员提供方便,从而减轻医疗资源的压力。
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[Pharmacological properties and clinical development overview of pertuzumab (genetical recombination), trastuzumab (genetical recombination) and vorhyaluronidase alfa (genetical recombination) (PHESGO® combination for ‍subcutaneous injection MA, IN)].

Pertuzumab and trastuzumab are anti-HER2 humanized monoclonal antibodies with different mechanisms of action. Their combination is expected to suppress intracellular HER2 signaling additively or synergistically. Their combination is widely recommended worldwide and has been established as a standard of care for HER2-positive breast cancer. However, improvement is required because of the prolonged time of intravenous infusion. Vorhyaluronidase alfa (rHuPH20) depolymerizes hyaluronan in the subcutaneous connective tissue. It's reported to increase the permeability and absorption levels of drugs. PHESGO® combination for subcutaneous injection MA/IN (PHESGO®) is a fixed-dose combination of pertuzumab, trastuzumab, and rHuPH20. A confirmatory phase III study (FeDeriCa) was conducted following a dose-finding phase I study (BO30185). Patients with HER2-positive early breast cancer were randomly assigned to receive either intravenous infusion of pertuzumab and trastuzumab or subcutaneous injection of PHESGO®, in combination with chemotherapy, to compare the pharmacokinetics (PK), efficacy and safety. A phase II study (PHranceSCa) was also conducted to assess patients' preference and satisfaction. Based on these results, population PK analysis, and other data, PHESGO® obtained marketing approval in Japan in September 2023 with indications for "HER2-positive breast cancer" and "advanced or recurrent HER2-positive colorectal cancer that has progressed following cancer chemotherapy and is not amenable to curative resection". By reducing the administration time, PHESGO® is expected to contribute to various needs of patients and improvement of their daily lives. Since drug preparation is not required, it can provide convenience to healthcare professionals, leading to stress reduction of medical resources as well.

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来源期刊
Folia Pharmacologica Japonica
Folia Pharmacologica Japonica Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
0.40
自引率
0.00%
发文量
132
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