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阿美替尼治疗转移性非小细胞肺癌:患者选择与特殊考量

Amivantamab in the Treatment of Metastatic NSCLC: Patient Selection and Special Considerations.

作者信息

Petrini Iacopo, Giaccone Giuseppe

机构信息

Medical Oncology, Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.

Weill-Cornell Medicine, Meyer Cancer Center, New York, NY, USA.

出版信息

Onco Targets Ther. 2022 Oct 12;15:1197-1210. doi: 10.2147/OTT.S329095. eCollection 2022.

Abstract

Amivantamab is a bispecific antibody that recognizes epidermal growth factor receptor (EGFR) and MET proto-oncogene (MET). In May 2021, the Food and Drug Administration gave an accelerated approval of amivantamab for the treatment of non-small cell lung cancer (NSCLC) patients with EGFR exon 20 insertions (Exon20ins) who progressed after platinum-based chemotherapy. Amivantamab prevents ligand binding to EGFR and MET and the dimerization of the receptors suppressing the downstream signal transduction. Moreover, amivantamab determines antibody dependent cellular cytotoxicity and down regulation of cell surface proteins through internalization of the receptor and trogocytosis. Preliminary results of the Phase I/IB CHRYSALIS trial demonstrated an objective response rate of 40% with a median duration of response of 11.1 months (95% CI 9.6-not reached) in 81 patients treated with amivantamab with pretreated NSCLC with Exon20ins EGFR mutations. In a different cohort of the CHRYSALIS trial, patients with Ex19del and L858R EGFR mutations were enrolled after progression on osimertinib. 121 and 45 patients received amivantamab or a combination with lazertinib, a third-generation tyrosine kinase inhibitor, respectively. The objective response rate was 19% and 36% in patients treated with amivantamab alone or in combination with lazertinib, with a median progression-free survival of 6.9 (95% CI: 3.2-5.3) and 11.1 (95% CI: 3.7-9.5) months, respectively. All 20 patients with Ex19del and L858R EGFR mutations who received amivantamab and lazertinib as their first line treatment achieved an objective response. Amivantamab is currently under evaluation in Phase III clinical trials for the first line treatment of NSCLCs with Exon20ins EGFR mutations in combination with chemotherapy (PAPILLON), for the first line therapy of Ex19del and L858R mutated NSCLCs in combination with lazertinib (MARIPOSA) and in combination with chemotherapy and lazertinib in NSCLCs who progressed on osimertinib (MARIPOSA-2).

摘要

阿米万他单抗是一种双特异性抗体,可识别表皮生长因子受体(EGFR)和MET原癌基因(MET)。2021年5月,美国食品药品监督管理局加速批准阿米万他单抗用于治疗经铂类化疗后病情进展的EGFR外显子20插入(Exon20ins)的非小细胞肺癌(NSCLC)患者。阿米万他单抗可防止配体与EGFR和MET结合以及受体二聚化,从而抑制下游信号转导。此外,阿米万他单抗可通过受体内化和穿胞作用确定抗体依赖性细胞毒性并下调细胞表面蛋白。I/IB期CHRYSALIS试验的初步结果显示,在81例接受过预处理的Exon20ins EGFR突变NSCLC患者中,使用阿米万他单抗治疗的客观缓解率为40%,中位缓解持续时间为11.1个月(95%CI 9.6 - 未达到)。在CHRYSALIS试验的另一组队列中,Ex19del和L858R EGFR突变患者在奥希替尼治疗进展后入组。分别有121例和45例患者接受了阿米万他单抗或与第三代酪氨酸激酶抑制剂拉泽替尼联合治疗。单独使用阿米万他单抗或与拉泽替尼联合治疗的患者的客观缓解率分别为19%和36%,中位无进展生存期分别为6.9(95%CI:3.2 - 5.3)和11.1(95%CI:3.7 - 9.5)个月。所有20例接受阿米万他单抗和拉泽替尼作为一线治疗的Ex19del和L858R EGFR突变患者均实现了客观缓解。阿米万他单抗目前正在进行III期临床试验评估,用于与化疗联合一线治疗具有Exon20ins EGFR突变的NSCLC(PAPILLON试验),与拉泽替尼联合一线治疗Ex19del和L858R突变的NSCLC(MARIPOSA试验),以及与化疗和拉泽替尼联合用于在奥希替尼治疗中进展的NSCLC(MARIPOSA - 2试验)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f01e/9555392/656b2156f45c/OTT-15-1197-g0001.jpg

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