Ou Sai-Hong Ignatius, Weitz Michael, Jalas John R, Kelly Daniel F, Wong Vanessa, Azada Michele C, Quines Oliver, Klempner Samuel J
Division of Hematology-Oncology, Department of Medicine, University of California Irvine School of Medicine, Orange, CA 92868, United States; Chao Family Comprehensive Cancer Center, Orange, CA 92868, United States.
Department of Emergency Medicine, Providence Saint John's Health Center, 2121 Santa Monica Blvd., Santa Monica, CA 90404, United States.
Lung Cancer. 2016 Jun;96:15-8. doi: 10.1016/j.lungcan.2016.03.008. Epub 2016 Mar 26.
Alectinib is a second generation ALK inhibitor that has significant clinical activity in central nervous system (CNS) metastases in anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer (NSCLC). Pseudoprogression (PsP) due to radiation necrosis during alecitnib treatment of central nervous system (CNS) metastases from ALK-rearranged NSCLC as been reported. Hence, distinguishing radiation-related PsP from alectinib-induced radiographic changes is important to avoid erroneous early trial discontinuation and abandonment of an effective treatment. However, it remains difficult to assess casuality of radiation necrosis is related to recent direct radiation or induced by alectinib treatment or both. It is also unknown how long from previous radiation can alectinib still induce radiation necrosis. Here we reported a crizotinib-refractory ALK-positive NSCLC patient who develop radiation necrosis in one of his metastatic CNS lesions after approximately 12 months of alectinib treatment who otherwise had on-going CNS response on alectinib. His most recent radiation to his CNS metastases was 7 years prior to the start of alectinib. This case illustrates that in the setting of pror CNS radiation, given the significant clinical activity of alectinib in CNS metastases in ALK-positive NSCLC patients the risk of CNS radiation necrosis remains long after previous radiation to the CNS metastases has been completed and can occur after durable response of treatment.
阿来替尼是第二代间变性淋巴瘤激酶(ALK)抑制剂,在ALK重排的非小细胞肺癌(NSCLC)的中枢神经系统(CNS)转移中具有显著的临床活性。已有报道称,在使用阿来替尼治疗ALK重排的NSCLC的中枢神经系统转移时,会出现因放射性坏死导致的假性进展(PsP)。因此,区分与放疗相关的PsP和阿来替尼引起的影像学变化对于避免错误地提前终止试验和放弃有效治疗很重要。然而,评估放射性坏死的因果关系是与近期的直接放疗有关,还是由阿来替尼治疗引起,抑或是两者共同作用,仍然很困难。此外,也不清楚在先前放疗后多长时间,阿来替尼仍可诱发放射性坏死。在此,我们报告了1例克唑替尼难治性ALK阳性NSCLC患者,在接受阿来替尼治疗约12个月后,其1个CNS转移病灶出现放射性坏死,而该患者在其他方面对阿来替尼仍有持续的CNS反应。他最近一次对CNS转移灶的放疗是在开始使用阿来替尼的7年前。该病例表明,在既往有CNS放疗的情况下,鉴于阿来替尼在ALK阳性NSCLC患者的CNS转移中具有显著的临床活性,在既往对CNS转移灶的放疗完成后很长时间内,CNS放射性坏死的风险依然存在,并且可能在治疗出现持久反应后发生。