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小分子 MET 抑制剂治疗的 MET 外显子 14 突变型非小细胞肺癌患者外周水肿的管理。

Management of Peripheral Edema in Patients with MET Exon 14-Mutated Non-small Cell Lung Cancer Treated with Small Molecule MET Inhibitors.

机构信息

Department of Thoracic Medical Oncology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research (JFCR), 3-8-31 Ariake, Koto-ku, Tokyo, 135-8550, Japan.

Department of Thoracic Oncology, Kanagawa Cancer Center, 2-3-2 Nakao, Asahi-ku, Yokohama, Kanagawa, 241-8515, Japan.

出版信息

Target Oncol. 2022 Sep;17(5):597-604. doi: 10.1007/s11523-022-00912-y. Epub 2022 Sep 10.

Abstract

Small molecule mesenchymal-epithelial transition (MET) inhibitors, such as crizotinib, capmatinib, and tepotinib, are treatment options for metastatic non-small cell lung cancer (NSCLC) in adult patients whose tumors have a mutation that leads to MET exon 14 skipping. In clinical trials, these MET inhibitors were associated with a high incidence of peripheral edema, although this was generally mild-to-moderate in severity. There is limited information about the mechanism involved in MET inhibitor-induced peripheral edema. Perturbation of hepatocyte growth factor (HGF)/MET signaling may disrupt the permeability balance in the vascular endothelium and thus promote edema development. Another potential mechanism is through effects on renal function, although this is unlikely to be the primary mechanism. Because edema is common in cancer patients and may not necessarily be caused by the cancer treatment, or other conditions that have similar symptoms to peripheral edema, a thorough assessment is required to ascertain the underlying cause. Before starting MET-inhibitor therapy, patients should be educated about the possibility of developing peripheral edema. Patient limb volume should be measured before initiating treatment, to aid assessment if symptoms develop. Since the exact mechanism of MET inhibitor-induced edema is unknown, management is empiric, with common approaches including compression stockings, specific exercises, massage, limb elevation, and/or diuretic treatment. Although not usually required, discontinuation of MET inhibitor treatment generally resolves peripheral edema. Early diagnosis and management, as well as patient information and education, are vital to decrease the clinical burden associated with edema, and to reinforce capmatinib treatment adherence.

摘要

小分子间质-上皮转化(MET)抑制剂,如克唑替尼、卡马替尼和特泊替尼,是治疗具有导致 MET 外显子 14 跳跃突变的肿瘤的成年转移性非小细胞肺癌(NSCLC)患者的选择。在临床试验中,这些 MET 抑制剂与外周水肿的高发生率相关,尽管其严重程度通常为轻至中度。关于 MET 抑制剂引起的外周水肿涉及的机制信息有限。肝细胞生长因子(HGF)/MET 信号的干扰可能破坏血管内皮的通透性平衡,从而促进水肿的发展。另一个潜在的机制是通过对肾功能的影响,尽管这不太可能是主要机制。由于水肿在癌症患者中很常见,并且不一定是由癌症治疗或其他具有类似外周水肿症状的疾病引起的,因此需要进行彻底评估以确定潜在的原因。在开始 MET 抑制剂治疗之前,应告知患者发生外周水肿的可能性。在开始治疗前应测量患者肢体的体积,以便在出现症状时进行评估。由于 MET 抑制剂引起水肿的确切机制尚不清楚,因此治疗是经验性的,常见的方法包括压缩袜、特定运动、按摩、肢体抬高和/或利尿剂治疗。尽管通常不需要,但停用 MET 抑制剂治疗通常可解决外周水肿问题。早期诊断和管理,以及患者信息和教育,对于减轻与水肿相关的临床负担以及加强卡马替尼治疗依从性至关重要。

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