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首页> 外文期刊>Cancer: A Journal of the American Cancer Society >A Phase 1 Study of Cetuximab and Lapatinib in Patients With Advanced Solid Tumor Malignancies
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A Phase 1 Study of Cetuximab and Lapatinib in Patients With Advanced Solid Tumor Malignancies

机译:西妥昔单抗和拉帕替尼在晚期实体瘤恶性肿瘤患者中的1期研究

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摘要

BACKGROUNDAcquired resistance to antiepidermal growth factor receptor (anti-EGFR) therapy may be caused by EGFR-v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2 (ErbB2) heterodimerization and pathway reactivation. In preclinical studies, inhibiting ErbB2 blocked this resistance mechanism and resensitized cells to anti-EGFR therapy. Cetuximab targets EGFR, whereas lapatinib inhibits both EGFR and ErbB2. The objective of this phase 1 trial was to assess the safety, dose-limiting toxicities (DLTs), and maximum tolerated doses (MTDs) of cetuximab and lapatinib in patients with solid tumors.
机译:背景技术对表皮生长因子受体(anti-EGFR)的抗药性可能是由EGFR-v-erb-b2禽红细胞白血病病毒病毒癌基因同源物2(ErbB2)异源二聚化和途径重新激活引起的。在临床前研究中,抑制ErbB2可阻断这种耐药机制,并使细胞对抗EGFR治疗敏感。西妥昔单抗靶向EGFR,而拉帕替尼同时抑制EGFR和ErbB2。这项1期试验的目的是评估实体瘤患者西妥昔单抗和拉帕替尼的安全性,剂量限制毒性(DLT)和最大耐受剂量(MTD)。

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