ALK Inhibitors Do Not Increase Sensitivity to Radiation in EML4-ALK Non-small Cell Lung Cancer

Anticancer Res. 2020 Sep;40(9):4937-4946. doi: 10.21873/anticanres.14497.

Abstract

Background/aim: ALK inhibitors like Crizotinib, Ceritinib and Alectinib are targeted therapies used in patients with anaplastic lymphoma kinase (ALK)-positive, advanced non-small cell lung cancer (NSCLC). Since in this tumor entity radiotherapy is employed sequentially or concomitantly, potential synergistic effects were investigated, which may support the hypothesis of induced radiosensitization by using ALK inhibitors.

Materials and methods: Two cell lines expressing wild-type (WT) or echinoderm microtubule-associated protein-like 4 (EML4)-ALK were treated with ALK inhibitors, followed by irradiation. Cell survival, cell death, cell cycle and phosphorylation of H2A histone family, member X (H2AX) were examined.

Results: Combined treatment with ALK-inhibitors plus 10 Gy-irradiation led to effects similar to those of sole radiotherapy, but was more effective than sole drug treatment.

Conclusion: There is no clear evidence of sensitization to radiation by treating EML4-ALK mutated cells with ALK inhibitors.

Keywords: ALK inhibitors; Alectinib; Ceritinib; Crizotinib; NSCLC; anaplastic lymphoma kinase; radiation.

MeSH terms

  • Anaplastic Lymphoma Kinase / antagonists & inhibitors*
  • Antineoplastic Agents / pharmacology*
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Carcinoma, Non-Small-Cell Lung / therapy*
  • Cell Cycle / radiation effects
  • Cell Death / drug effects
  • Cell Death / radiation effects
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Cell Survival / radiation effects
  • Chemoradiotherapy
  • Drug Resistance, Neoplasm / genetics
  • Humans
  • Lung Neoplasms / pathology
  • Lung Neoplasms / therapy*
  • Mutation
  • Oncogene Proteins, Fusion / genetics*
  • Protein Kinase Inhibitors / pharmacology*

Substances

  • Antineoplastic Agents
  • EML4-ALK fusion protein, human
  • Oncogene Proteins, Fusion
  • Protein Kinase Inhibitors
  • ALK protein, human
  • Anaplastic Lymphoma Kinase