St. Luke's Regional Cancer Center, St. Luke's Hospital, Duluth, MN, USA.
J Oncol Pharm Pract. 2020 Dec;26(8):2028-2030. doi: 10.1177/1078155220918644. Epub 2020 May 31.
Alectinib is an oral tyrosine kinase inhibitor currently recommended by the National Comprehensive Cancer Network (NCCN) as the preferred first-line treatment option for the treatment of metastatic anaplastic lymphoma kinase (ALK) gene rearrangement-positive non-small cell lung cancer (NSCLC). Skin toxicity is a known adverse effect of this medication, yet current recommendations are unclear regarding how to best manage patients who develop severe skin toxicity while taking alectinib.
Here, we describe a case of successful rechallenge with alectinib by utilizing a desensitization procedure in a patient who had developed severe alectinib-induced skin toxicity about two weeks into treatment. Upon resolution of the initial skin toxicity symptoms, the patient was rechallenged with alectinib using a modified version of a previously published desensitization procedure. The patient tolerated the rechallenge with no recurrence of skin toxicity or other adverse effects and was able to continue treatment with alectinib.
Alectinib is currently recommended as the preferred first-line treatment option for the treatment of metastatic anaplastic lymphoma kinase gene rearrangement-positive NSCLC due to improved progression-free survival when compared to crizotinib. The development of skin toxicity can lead to early discontinuation of alectinib treatment, forcing providers and patients to select alternative, potentially less effective options. This case report provides evidence that patients who have experienced severe skin toxicity due to alectinib may be able to continue this first-line treatment option by rechallenging them using a desensitization procedure.
阿来替尼是一种口服酪氨酸激酶抑制剂,目前被国家综合癌症网络(NCCN)推荐为治疗转移性间变性淋巴瘤激酶(ALK)基因重排阳性非小细胞肺癌(NSCLC)的首选一线治疗方案。皮肤毒性是该药物已知的不良反应,但目前关于如何最好地管理在服用阿来替尼时发生严重皮肤毒性的患者的建议尚不清楚。
在这里,我们描述了一例在治疗约两周时发生严重阿来替尼诱导皮肤毒性的患者,通过脱敏程序成功重新使用阿来替尼的病例。在初始皮肤毒性症状缓解后,患者使用之前发表的脱敏程序的修改版本重新接受阿来替尼治疗。患者耐受重新挑战,没有再次出现皮肤毒性或其他不良反应,能够继续使用阿来替尼治疗。
与克唑替尼相比,阿来替尼作为治疗间变性淋巴瘤激酶基因重排阳性 NSCLC 的首选一线治疗方案,可改善无进展生存期,因此被推荐。皮肤毒性的发展可能导致阿来替尼治疗的早期停药,迫使提供者和患者选择替代的、潜在效果较差的选择。本病例报告提供了证据表明,因阿来替尼而发生严重皮肤毒性的患者可以通过脱敏程序重新挑战他们,从而继续使用这种一线治疗方案。