ALK in cancer: from function to therapeutic targeting.

in Nature reviews. Cancer by Claudia Voena, Chiara Ambrogio, Fabio Iannelli, Roberto Chiarle

TLDR

  • ALK inhibitors have revolutionized the treatment of ALK-driven tumours, but resistance and recurrence remain major challenges. New approaches, including ALK-specific immune therapies and combination therapies, are needed to improve outcomes.

Abstract

Anaplastic lymphoma kinase (ALK) is a receptor tyrosine kinase (RTK) that acts as an oncogenic driver in solid and haematological malignancies in both children and adults. Although ALK-expressing (ALK) tumours show strong initial responses to the series of ALK inhibitors currently available, many patients will develop resistance. In this Review, we discuss recent advances in ALK oncogenic signalling, together with existing and promising new modalities to treat ALK-driven tumours, including currently approved ALK-directed therapies, namely tyrosine kinase inhibitors, and novel approaches such as ALK-specific immune therapies. Although ALK inhibitors have changed the management and clinical history of ALKtumours, they are still insufficient to cure most of the patients. Therefore, more effort is needed to further improve outcomes and prevent the tumour resistance, recurrence and metastatic spread that many patients with ALKtumours experience. Here, we outline how a multipronged approach directed against ALK and other essential pathways that sustain the persistence of ALKtumours, together with potent or specific immunotherapies, could achieve this goal. We envision that the lessons learned from treating ALKtumours in the clinic could ultimately accelerate the implementation of innovative combination therapies to treat tumours driven by other tyrosine kinases or oncogenes with similar properties.

Overview

  • The study focuses on the role of anaplastic lymphoma kinase (ALK) as an oncogenic driver in solid and haematological malignancies, as well as recent advances in ALK oncogenic signalling and treatment modalities.
  • The article discusses the efficacy of ALK inhibitors in treating ALK-driven tumours, including tyrosine kinase inhibitors and ALK-specific immune therapies.
  • The study aims to identify new strategies to improve outcomes and prevent resistance, recurrence, and metastatic spread in patients with ALK-driven tumours.

Comparative Analysis & Findings

  • ALK inhibitors have shown strong initial responses in treating ALK-driven tumours, but many patients develop resistance over time.
  • Novel approaches such as ALK-specific immune therapies and combination therapies directed against ALK and other essential pathways may improve treatment outcomes.
  • While ALK inhibitors have changed the management of ALK-driven tumours, they are still insufficient to cure most patients.

Implications and Future Directions

  • A multipronged approach incorporating ALK inhibitors, immunotherapies, and combination therapies may be necessary to achieve better outcomes in patients with ALK-driven tumours.
  • The lessons learned from treating ALK-driven tumours may accelerate the development of innovative combination therapies for tumours driven by other tyrosine kinases or oncogenes.
  • Further research is needed to identify new strategies to prevent resistance, recurrence, and metastatic spread in patients with ALK-driven tumours.