Successful treatment with crizotinib after alectinib-induced interstitial lung disease.
Ning ZhuShanhong LinLei HeLinfeng WangWeiliang KongChao CaoPublished in: SAGE open medical case reports (2021)
Although alectinib is a well-tolerated and highly effective inhibitor of a second-generation anaplastic lymphoma kinase, special attention should be paid to the possibility of potentially severe and fatal adverse events such as interstitial pneumonia. We report a case of a patient with advanced non-small cell lung cancer treated with alectinib who developed immunohistochemically positive anaplastic lymphoma kinase (ALK(IHC +)) . However, due to the rapid emergence of drug-induced interstitial lung disease, alectinib treatment was halted. Once the interstitial lung disease had been successfully treated, we reluctantly chose crizotinib as a second-line treatment for ALK + NSCLC in this patient as he refused all other available treatments. Contrary to expectation, crizotinib performed well both in terms of its safety and efficacy. Our results suggest that crizotinib may provide a promising therapy option for patients with ALK + NSCLC accompanied by alectinib-induced interstitial lung disease. To our knowledge, this is a rare report of successful treatment of ALK + NSCLC with crizotinib after alectinib-induced interstitial lung disease.
Keyphrases
- interstitial lung disease
- advanced non small cell lung cancer
- systemic sclerosis
- drug induced
- epidermal growth factor receptor
- liver injury
- rheumatoid arthritis
- idiopathic pulmonary fibrosis
- high glucose
- diabetic rats
- tyrosine kinase
- healthcare
- case report
- diffuse large b cell lymphoma
- endothelial cells
- adverse drug
- protein kinase
- working memory
- stem cells
- early onset
- combination therapy
- extracorporeal membrane oxygenation
- intensive care unit
- cell therapy
- acute respiratory distress syndrome