Semitelou 2A, 115 28 Athens, Greece.
Anticancer Res. 2010 Mar;30(3):973-6.
Erlotinib is an oral, small-molecule targeting therapy which inhibits epidermal growth factor tyrosine kinase receptors. Erlotinib has been administered for the treatment of advanced pancreatic cancer and non-small cell lung cancer.
In the present report, unusual hematologic complications were detected after erlotinib was administered as second-line monotherapy in pretreated patients with advanced non-small cell lung cancer. Four patients pre-treated with cisplatin or its analog-based combinations, were evaluated. Erlotinib was given at a dose of 150 mg daily. In cases of intolerable adverse reactions, the dose was either reduced to 100 mg daily or treatment was interrupted for a maximum of two weeks.
Serious hematologic toxicity (or complications) developed in these 4 patients after 4-8.5 months of treatment. Two patients developed leukemias (AML, CML) and two, myelodysplastic syndrome.
Whether or not these hematologic complications were related to erlotinib treatment is comprehensively discussed.
厄洛替尼是一种口服的小分子靶向治疗药物,可抑制表皮生长因子酪氨酸激酶受体。厄洛替尼已被用于治疗晚期胰腺癌和非小细胞肺癌。
本报告介绍了 4 例接受以顺铂或其类似物为基础的联合化疗方案治疗后的晚期非小细胞肺癌患者,二线应用厄洛替尼单药治疗后出现的不常见血液学并发症。厄洛替尼的剂量为 150 mg/d。若出现不能耐受的不良反应,剂量减至 100 mg/d 或最多中断治疗 2 周。
这 4 例患者在接受厄洛替尼治疗 4-8.5 个月后出现严重的血液学毒性(或并发症)。其中 2 例发生白血病(AML、CML),2 例发生骨髓增生异常综合征。
全面讨论了这些血液学并发症是否与厄洛替尼治疗相关。