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Pharmacology · Chemotherapy: ALK-positive lung cancer
Sample itemA 45-year-old woman who has never smoked has lung adenocarcinoma with an EML4-ALK fusion on molecular testing. EGFR mutation is absent. Which oral targeted drug is appropriate?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. Crizotinib
EML4-ALK fusions drive a subset of lung adenocarcinomas, typically in young never-smokers. Crizotinib inhibits ALK and ROS1 tyrosine kinases, and newer ALK inhibitors such as alectinib are used in the same setting.
Option by option
A. Erlotinib
Erlotinib targets EGFR, and the EGFR mutation is absent here.
B. Vemurafenib
Vemurafenib inhibits BRAF V600E, which is not the driver in this tumour.
C. Crizotinib (correct)
Correct. Crizotinib inhibits the ALK fusion kinase.
D. Imatinib
Imatinib inhibits BCR-ABL, KIT and PDGFR, not ALK fusions.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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