JTO:克唑替尼治疗的ALK重排NSCLC患者的长期结局如何

2017-06-14 陶白 肿瘤资讯

许多研究显示,克唑替尼对ALK重排的NSCLC患者有效,但是更长期的患者结局却鲜有报道。美国贝斯以色列女执事医疗中心血液学/肿瘤学科的Daniel B. Costa博士报道了两例ALK重排的NSCLC病例的5年PFS和OS,并回顾性审查了该中心的ALK FISH检测阳性病例,相关研究结果6月2日已被《JTO》所接收。

许多研究显示,克唑替尼对ALK重排的NSCLC患者有效,但是更长期的患者结局却鲜有报道。美国贝斯以色列女执事医疗中心血液学/肿瘤学科的Daniel B. Costa博士报道了两例ALK重排的NSCLC病例的5年PFS和OS,并回顾性审查了该中心的ALK FISH检测阳性病例,相关研究结果6月2日已被《JTO》所接收。

过去的十年,见证了间变性淋巴瘤激酶(ALK)重排的非小细胞肺癌(NSCLC)从不熟悉的疾病到最成功的精准医疗案例的演变。目前,4种ALK酪氨酸激酶抑制剂(TKI)已经获批用于晚期ALK重排的NSCLC的治疗中:克唑替尼、色瑞替尼、艾乐替尼和brigatinib。克唑替尼是首个获批的多靶点ALK抑制剂(2011年获批),然而,患者更长期的结局却鲜有报道。因此,研究人员进行了一项病例报告,旨在评估接受克唑替尼作为初始ALK靶向治疗的患者中,其5年无进展生存率(PFS)和总生存率(OS)。

病例1为76岁的不吸烟女性,该患者患有复发性晚期ALK重排的肺腺癌(ALK FISH检测显示,78%的细胞阳性)。该患者接受克唑替尼250mg每天两次,随后因胃肠道不良事件和疲劳而降低剂量到250mg每天一次。治疗后,她获得了部分应答,并维持了超过76个月(图1A)。病例2为47岁的不吸烟男性,患有IV期ALK重排的肺腺癌(ALK FISH检测显示,58%的细胞阳性)。该患者接受了克唑替尼250mg每天两次,并实现了部分应答,维持了超过60个月(图1B)。为了更好理解其他病例的长期疾病控制情况,研究人员回顾性审查了其医疗机构中的AKL重排肺癌患者对,并评估了克唑替尼使用时间、其他AKL抑制剂使用情况、PFS、OS和因毒性而导致的停药情况。研究者从图表中,回顾性提取了病理学数据、肿瘤基因型、AKL TKI的类型/剂量、X线图像和生存数据等。

研究队列由45/835(5.3%)例ALK FISH检测阳性的病例组成。其中,26例晚期疾病患者(IV期或复发)接受克唑替尼作为初始ALK抑制剂治疗(图2)。患者的中位年龄为57岁(范围:29~81岁),13例(50%)为女性,15例(37%)为不吸烟者(每年中位0包香烟【范围:0~100包】),民族/种族具有差异(22例白人,4例亚裔),所有患者都为NSCLC(24例肺腺癌,1例腺鳞癌,1例鳞癌)。虽然克唑替尼在多数病例中耐受性良好,但是3例患者因毒性而在疾病进展前停止服用(图1)。另有11例患者在初始放射学证实为疾病进展后继续使用克唑替尼,10例患者接受了下一代ALK抑制剂(图2)。克唑替尼治疗的患者的中位PFS为9个月,估计5年PFS为9%(表3A)。中位OS为48个月,估计5年OS为36%(图3B)。

点评:如今,多个获批的ALK抑制剂可缓解晚期ALK重排NSCLC。本研究的病例证实了多个关于疾病和TKI作用的结论:(1)克唑替尼单一治疗可使少数患者(<10%)实现长期疾病控制(PFS ≥5年);(2)疾病进展前继续使用克唑替尼在一些患者中是一种有效的策略(尤其是肿瘤部位可被其他治疗方法减轻的患者,即放疗减轻脑转移);(3)序贯使用ALK TKI可延长该群体的中位OS至将近4年,初始单一或序贯ALK TKI后,超过三分之一的患者可存活5年。
图1:2例晚期ALK重排的肺癌患者中,初始克唑替尼治疗后≥5年(≥60个月)的病例。A:病例1,开始克唑替尼前和开始克唑替尼第6年的颈部计算机断层扫描(CT)结果。红圈表示右锁骨上淋巴结肿大的反应。B:病例2,开始克唑替尼前和开始克唑替尼第5年的胸部CT结果。红圈表示胸大肌下淋巴结反应。
图2:26例晚期ALK重排肺癌患者中,初始克唑替尼后第一个5年(60个月)的ALK抑制剂使用情况、抗癌治疗和姑息治疗情况。ALK TKI类型、化疗或最佳支持疗法以不同的颜色表示。实体瘤疗效评价标准(RECIST)确定的疾病进展以P表示,克唑替尼的毒性以T表示,放疗的使用以X表示,失访以L表示,死亡以D表示,持续治疗/生存以+表示。
图3:ALK重排肺癌患者初始克唑替尼治疗后的无进展生存情况和总生存情况。A:具有中位值和每年评估值的无进展生存率曲线。B:具有中位值和每年评估值的总生存率曲线。使用REDCap电子数据采集系统收集和管理数据。在确诊的肿瘤样本中使用ALK荧光原位杂交(FISH)分离探针进行肿瘤基因分型。当审查目标/非目标X线图像时,使用实体瘤疗效评价标准。初始克唑替尼后,按月计算PFS和OS(舍入至最近的整月)。使用Kaplan-Meier方法评估PFS和OS。使用GraphPad Prism6软件进行统计学分析,绘制曲线。

原始出处:

Deepa Rangachari,Xiuning Le, MD,et al.Cases of ALK-rearranged lung cancer with 5-year progression-free survival with crizotinib as initial precision therapy.
Journal of Thoracic Oncology.DOI: http://dx.doi.org/10.1016/j.jtho.2017.06.002

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    2017-06-16 cqykthl

    间变性淋巴瘤的接抗剂

    0

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    2017-06-16 日月生辉

    药物治疗取得这种效果不错了

    0

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    2017-06-16 luominglian113

    学习了,谢谢分享

    0

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    2017-06-15 一个尘埃

    学习了,谢谢分享!

    0

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    2017-06-15 榄枷檬

    谢谢分享

    0

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