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ALK fusion gene positive lung cancer and 3 cases treated with an inhibitor for ALK kinase activity

机译:ALK融合基因阳性肺癌和3例ALK激酶活性抑制剂治疗

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Background: Anaplastic lymphoma kinase (ALK) fusion gene-positive lung cancer accounts for 4-5% of non-small cell lung carcinoma. A clinical trial of the specific inhibitor of ALK fusion-type tyrosine kinase is currently under way. Methods: ALK fusion gene products were analyzed immunohistochemically with the materials obtained by surgery or by endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA). The echinoderm microtubule-associated protein-like 4(EML4)-ALK or kinesin family member 5B (KIF5B)-ALK translocation was confirmed by the reverse transcription polymerase chain reaction (RT-PCR) and fluorescence in situ hybridization (FISH). After eligibility criteria were met and informed consent was obtained, 3 patients were enrolled for the Pfizer Study of Crizotinib (PF02341066), Clinical Trial A8081001, conducted at Seoul National University. Results: Out of 404 cases, there were 14 of EML4-ALK non-small cell carcinoma (NSCLC) and one KIF5B-ALK NSCLC case (8 men, 7 women; mean age, 61.9 years, range 48-82). Except for 2 light smokers, all patients were non-smokers. All cases were of adenocarcinoma with papillary or acinar subtypes. Three were of stage IA, 5 of stage IIIA, 1 of stage IIIB and 6 of stage IV. Ten patients underwent thoracotomy, 3 received chemotherapy and 2 only best supportive care (BSC). One BSC and 2 chemotherapy cases were enrolled for the clinical trial. Patients with advanced stages who received chemotherapy or best supportive care were younger (54.0 ± 6.3) than those who were surgically treated (65.8 ± 10.1) (p< 0.05).The powerful effect of ALK inhibitor on EML4-ALK NSCLC was observed. Soon after its administration, almost all the multiple bone and lymph node metastases quickly disappeared. Nausea, diarrhea and the persistence of a light image were the main side effects, but they diminished within a few months. Conclusion: ALK-fusion gene was found in 3.7% (15/404) NSCLC cases and advanced disease with this fusion gene was correlated with younger generation. The ALK inhibitor presented in this study is effective in EML4-ALK NSCLC cases. A further study will be necessary to evaluate the clinical effectiveness of this drug.
机译:背景:间变性淋巴瘤激酶(ALK)融合基因阳性的肺癌占非小细胞肺癌的4-5%。目前正在进行ALK融合型酪氨酸激酶特异性抑制剂的临床试验。方法:采用手术或支气管内超声引导经支气管针吸术(EBUS-TBNA)获得的材料对ALK融合基因产物进行免疫组织化学分析。通过逆转录聚合酶链反应(RT-PCR)和荧光原位杂交(FISH)证实了棘皮动物微管相关蛋白样4(EML4)-ALK或驱动蛋白家族成员5B(KIF5B)-ALK易位。符合资格标准并获得知情同意后,在首尔国立大学进行了3例患者的辉瑞研究克唑替尼(PF02341066),临床试验A8081001。结果:在404例病例中,有14例EML4-ALK非小细胞癌(NSCLC)和1例KIF5B-ALK NSCLC病例(男8例,女7例;平均年龄61.9岁,范围48-82)。除两名轻度吸烟者外,所有患者均为非吸烟者。所有病例均为具有乳头状或腺泡状亚型的腺癌。其中三个是IA阶段,五个是IIIA阶段,一个是IIIB阶段,六个是IV阶段。 10例患者接受了开胸手术,3例接受了化疗,2例仅接受了最佳支持治疗(BSC)。 1例BSC和2例化疗病例被纳入临床试验。接受化疗或最佳支持治疗的晚期患者比接受手术治疗的患者(65.8±10.1)年轻(54.0±6.3)(p <0.05)。观察到ALK抑制剂对EML4-ALK NSCLC的有效作用。给药后不久,几乎所有的多处骨和淋巴结转移迅速消失。主要的副作用是恶心,腹泻和残影不清是主要的副作用,但在几个月内就消失了。结论:在3.7%(15/404)NSCLC患者中发现了ALK融合基因,该基因的晚期疾病与年轻一代有关。在这项研究中提出的ALK抑制剂对EML4-ALK NSCLC病例有效。有必要进行进一步的研究以评估这种药物的临床有效性。

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