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Guideline-based case report: neoadjuvant alectinib in ALK-rearranged stage IIIB lung cancer

Guideline-based case report: neoadjuvant alectinib in ALK-rearranged stage IIIB lung cancer
Photo by Julia Koblitz / Unsplash
Key Takeaway
Consider neoadjuvant alectinib as a potential strategy in ALK-rearranged NSCLC, but evidence is limited to a single case.

This publication is a case report presented within a guideline framework, describing the use of neoadjuvant alectinib (600 mg twice daily) with an imaging response-adapted strategy in a 57-year-old never-smoking woman with ALK-rearranged stage IIIB lung adenocarcinoma. The report details the patient's course from diagnosis through surgery and follow-up.

At first restaging CT, the patient achieved a partial response with a 76% reduction in primary tumor diameter and a 50% reduction in the short axis of station 7 lymph node. After surgery, pathological examination showed a major pathological response (MPR). The patient remained disease-free at the last follow-up 33 months post-surgery.

No clinically significant treatment-related adverse events were reported. The authors note that this case offers a refined perioperative paradigm for ALK-rearranged NSCLC, but the evidence is limited to a single patient.

Key limitations include the lack of a comparator, small sample size (n=1), and absence of reported p-values or confidence intervals. As a case report, these findings cannot be generalized to broader populations, and no causal claims can be made. The practice relevance is illustrative rather than definitive.

Study Details

Study typeGuideline
EvidenceLevel 5
PublishedMay 2026
View Original Abstract ↓
BackgroundAlectinib, a second-generation ALK inhibitor, is established as a first-line treatment for advanced ALK-positive NSCLC and as adjuvant therapy following resection for early-stage disease. However, its role as a neoadjuvant therapy remains under investigation.Case presentationWe report a 57-year-old never-smoking woman diagnosed with stage IIIB (cT4N2M0) ALK-rearranged lung adenocarcinoma. After the initial multidisciplinary team (MDT) convening, a consensus was reached to initiate neoadjuvant alectinib (600 mg twice daily), with the first response evaluation scheduled at 4 weeks. The first restaging computed tomography (CT) demonstrated a significant partial response (PR), characterized by a 76% reduction in the primary tumor diameter and a 50% reduction in the short axis of the station 7 lymph node. In light of this robust response which already met surgical criteria, the MDT decided to proceed with a second 4-week consolidation cycle to maximize the pathological response prior to surgery. Following the second cycle, subsequent imaging confirmed further tumor regression. The patient then underwent successful R0 resection, with pathology confirming a major pathological response (MPR). Adjuvant alectinib was resumed on postoperative day 2. At the last follow-up (33 months post-surgery), the patient remains disease-free with no clinically significant treatment-related adverse events.ConclusionThis case illustrates the successful personalization of neoadjuvant alectinib by employing an imaging response-adapted strategy. This strategy utilized dynamic imaging assessments to guide the scheduling of the surgical procedure, culminating in a deep pathological response and prolonged disease-free survival, thereby offering a refined perioperative paradigm for ALK-rearranged NSCLC.
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