Lutetium Lu 177 vipivotide tetraxetan: A literature review.

IF 1.3 4区 医学 Q4 ONCOLOGY
Journal of Oncology Pharmacy Practice Pub Date : 2026-09-01 Epub Date: 2025-11-11 DOI:10.1177/10781552251392083
Grace Morrison, Lisa M Holle
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引用次数: 0

Abstract

To review pharmacology, pharmacokinetics, therapeutic use, product safety/description and perspectives on use of lutetium Lu 177 vipivotide tetraxetan in patients with metastatic castration-resistant prostate cancer (mCRPC). Data sources: A literature search was conducted using PubMed/Dynamed (October 2013-May 2025), limited to English language, humans, clinical trials, case reports, and guidelines. Data summary: Lutetium Lu 177 vipivotide tetraxetan is comprised of the beta-emitting radioisotope lutetium Lu-177 linked to a peptide, vipivotide tetraxetan, which binds to cells expressing prostate-specific membrane antigen (PSMA), resulting in cell death from the radiation. Kidney excretion may result in increased renal toxicity in patients with reduced renal function. Based on 2 phase III clinical trials, lutetium Lu 177 vipivotide tetraxetan 7.4 GBq administered intravenously every 6 weeks for up to 6 doses is effective in patients with mCRPC and PSMA-positive metastases after progressing on an androgen receptor pathway inhibitor and docetaxel therapy or an androgen receptor pathway inhibitor alone, by significantly improving radiographic progression-free survival. It is generally well tolerated, with asthenia/fatigue, dry mouth, mild nausea and low-grade anemia most commonly occurring. Severe adverse drug reactions are uncommon. It should only be administered by trained personnel in a designated clinical setting with existing radiation safety protocols. Patients must limit close contact, use precautions with using the bathroom and other daily activities in days following treatment. Patient education is necessary to ensure safe daily practices. Several ongoing trials are evaluating lutetium Lu 177 vipivotide tetraxetan in combination with other anticancer agents for treatment of mCRPC, using different dosing strategies, or in other settings (metastatic castration-sensitive prostate cancer and early-stage prostate cancer). Conclusion: Lutetium Lu 177 vipivotide tetraxetan is an effective and well tolerated treatment for patients with mCRPC, PSMA-positive metastases after progressing on an androgen receptor pathway inhibitor ± docetaxel. Ongoing studies evaluating its use in earlier disease stages and with different dosing strategies, will better define the role of this therapy in the treatment of prostate cancer.

目的:综述lu177 vipivotide tetraxetan在转移性去势抵抗性前列腺癌(mCRPC)患者中的药理学、药代动力学、治疗用途、产品安全性/描述和应用前景。数据来源:使用PubMed/Dynamed(2013年10月- 2025年5月)进行文献检索,仅限于英语、人类、临床试验、病例报告和指南。数据摘要:Lutetium Lu 177 vipivotide tetraxetan是由释放β的放射性同位素Lutetium Lu-177与肽vipivotide tetraxetan连接而成,肽与表达前列腺特异性膜抗原(PSMA)的细胞结合,导致细胞因辐射死亡。肾脏排泄可能导致肾功能下降的患者肾毒性增加。基于2项III期临床试验,lutetium Lu 177 vipivotide tetraxetan 7.4 GBq每6周静脉注射最多6次,对于在雄激素受体途径抑制剂和多西他赛治疗或单独雄激素受体途径抑制剂治疗进展后的mCRPC和psm阳性转移患者有效,通过显着提高放射学无进展生存期。通常耐受性良好,最常见的症状是乏力/疲劳、口干、轻度恶心和低度贫血。严重的药物不良反应并不常见。它只能由训练有素的人员在指定的临床环境中按照现有的辐射安全规程进行管理。在治疗后的几天内,患者必须限制密切接触,使用浴室和其他日常活动时采取预防措施。患者教育是必要的,以确保安全的日常做法。一些正在进行的试验正在评估lutetium lu177 vipivotide tetraxetan与其他抗癌药物联合治疗mCRPC,使用不同的剂量策略,或在其他情况下(转移性去势敏感前列腺癌和早期前列腺癌)。结论:Lutetium Lu 177 vipivotide tetraxetan对于雄激素受体途径抑制剂±多西他赛进展后的mCRPC, psma阳性转移患者是一种有效且耐受性良好的治疗方法。正在进行的研究评估其在早期疾病阶段和不同剂量策略的使用,将更好地确定这种疗法在治疗前列腺癌中的作用。
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来源期刊
CiteScore
2.70
自引率
7.70%
发文量
276
期刊介绍: Journal of Oncology Pharmacy Practice is a peer-reviewed scholarly journal dedicated to educating health professionals about providing pharmaceutical care to patients with cancer. It is the official publication of the International Society for Oncology Pharmacy Practitioners (ISOPP). Publishing pertinent case reports and consensus guidelines...
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