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Retreatment of lung adenocarcinoma patients with gefitinib who had experienced favorable results from their initial treatment with this selective epidermal growth factor receptor inhibitor: a report of three cases.

机译:吉非替尼治疗的肺腺癌患者从使用这种选择性表皮生长因子受体抑制剂的初始治疗中获得了良好的效果:三例报道。

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Gefitinib is a selective inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinases, and shows favorable antitumor activity against chemorefractory non-small cell lung cancer (NSCLC). The majority of responders (patients who are sensitive to gefitinib), however, relapse within 1.5 years, indicating an acquired resistance to gefitinib. Here we report three chemotherapy refractory NSCLC patients who were retreated with gefitinib. All three cases were nonsmokers and showed an adenocarcinoma histology. While they had experienced successful control from their initial treatment with gefitinib for more than 12 months, gefitinib therapy was terminated because two cases (cases 1 and 3) relapsed during the therapy and case 2 suffered alveolar hemorrhage. After more than 7 months from the time of discontinuation of the initial gefitinib treatment, they were retreated with gefitinib, as further tumor progression was observed. Of the three cases, cases 1 and 2 were well controlled by retreatment with gefitinib monotherapy for more than 7 months, suggesting sensitivity to retreatment. Case 3 also showed a regression in size of several tumors, while some other lesions progressively enlarged and developed a malignant pleural effusion after 4 months. These observations suggest the possibility that retreatment with gefitinib might be useful when 1) initial treatment shows a favorable clinical response, and 2) there has been a period of time following the termination of the initial gefitinib treatment.
机译:吉非替尼是表皮生长因子受体(EGFR)酪氨酸激酶的选择性抑制剂,对化学难治性非小细胞肺癌(NSCLC)具有良好的抗肿瘤活性。但是,大多数应答者(对吉非替尼敏感的患者)在1.5年内复发,表明对吉非替尼有获得性耐药。在这里,我们报告了三名接受吉非替尼治疗的化疗难治性非小细胞肺癌患者。这三例均为非吸烟者,均表现出腺癌组织学。尽管他们从使用吉非替尼开始治疗以来就已经成功地控制了超过12个月,但由于有2例病例(病例1和3)在治疗期间复发,并且病例2出现了牙槽出血,因此吉非替尼治疗被终止。从最初的吉非替尼治疗终止起超过7个月后,由于观察到进一步的肿瘤进展,因此用吉非替尼重新治疗了它们。在这三例病例中,通过吉非替尼单药再治疗超过7个月可以很好地控制病例1和2,表明对再治疗敏感。病例3还显示出几个肿瘤的大小缩小,而其他一些病变在4个月后逐渐扩大并发展为恶性胸腔积液。这些观察结果表明,当1)初始治疗显示出良好的临床反应,以及2)初始吉非替尼治疗终止后有一段时间后,用吉非替尼复治可能有用。

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