A case of primary pulmonary atypical carcinoid with EML4-ALK rearrangement

Na Liu1, Jingjing Wang1, Xiao Fu1

  • 1Department of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, People's Republic of China.

Cancer Biology & Therapy
|September 28, 2019
PubMed

Insights

Anaplastic lymphoma kinase (ALK) rearrangement, rare in atypical carcinoid lung cancer, responded well to sequential targeted therapies. This approach offers significant clinical benefits for patients with advanced non-small cell lung cancer (NSCLC).

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Targeted therapy has transformed advanced non-small cell lung cancer (NSCLC) treatment, particularly for tumors with specific gene mutations.
  • Early detection of gene alterations through advanced diagnostics allows for personalized treatment strategies.

Observation:

  • A 52-year-old female presented with a pulmonary nodule, diagnosed as moderately differentiated atypical carcinoid (AC) post-surgery.
  • Anaplastic lymphoma kinase (ALK) rearrangement was identified in the AC, a rare occurrence.
  • The patient's cancer progressed despite chemotherapy and radiotherapy.

Findings:

  • Sequential administration of ALK-tyrosine kinase inhibitors (TKIs)—crizotinib, ceritinib, and alectinib—demonstrated significant clinical benefits.
  • This case highlights the efficacy of a sequential targeted therapy approach in managing advanced NSCLC with rare ALK rearrangements in AC.

Implications:

  • Understanding the clinical significance and resistance mechanisms of ALK rearrangement is crucial for optimizing lung cancer treatment.
  • ALK-TKIs represent a vital therapeutic option for NSCLC patients with ALK alterations, with sequential therapy offering a promising strategy.
  • Further research into ALK-TKI applications and resistance mechanisms is warranted to improve patient outcomes in lung cancer.

Related Concept Videos