4.7 Article

Therapy for Stage IV Non-Small-Cell Lung Cancer With Driver Alterations: ASCO and OH (CCO) Joint Guideline Update

Journal

JOURNAL OF CLINICAL ONCOLOGY
Volume 39, Issue 9, Pages -

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1200/JCO.20.03570

Keywords

-

Categories

Funding

  1. Genentech/Roche
  2. Novartis
  3. Celgene
  4. Bristol-Myers Squibb
  5. AstraZeneca
  6. University of Texas Southwestern Medical Center -Simmons Cancer Center
  7. Merck
  8. G1 Therapeutics
  9. Neon Therapeutics
  10. Takeda
  11. Nektar
  12. Celldex
  13. Clovis Oncology
  14. Daiichi Sankyo
  15. EMD Serono
  16. Astellas Pharma
  17. GRAIL
  18. Transgene
  19. Aeglea Biotherapeutics
  20. Ipsen
  21. BIND Therapeutics
  22. Eisai
  23. ImClone Systems
  24. Immunogen
  25. Janssen Oncology
  26. MedImmune
  27. Molecular Partners
  28. Agios
  29. GlaxoSmithKline
  30. Tesaro
  31. Cyteir
  32. Apollomics

Ask authors/readers for more resources

The updated guidelines provide evidence-based recommendations for systemic therapy in stage IV NSCLC patients with driver alterations, based on systematic reviews of randomized controlled trials and meeting abstracts. These recommendations emphasize the importance of testing for targetable mutations before initiating therapy, and highlight the use of targeted therapies for specific alterations like ROS-1 fusions and BRAF V600e mutations.
PURPOSE To provide evidence-based recommendations updating the 2017 ASCO guideline on systemic therapy for patients with stage IV non-small-cell lung cancer (NSCLC) with driver alterations. A guideline update for systemic therapy for patients with stage IV NSCLC without driver alterations was published separately. METHODS The American Society of Clinical Oncology and Ontario Health (Cancer Care Ontario) NSCLC Expert Panel updated recommendations based on a systematic review of randomized controlled trials (RCTs) from December 2015 to January 2020 and meeting abstracts from ASCO 2020. RESULTS This guideline update reflects changes in evidence since the previous update. Twenty-seven RCTs, 26 observational studies, and one meta-analysis provide the evidence base (total 54). Outcomes of interest included efficacy and safety. Additional literature suggested by the Expert Panel is discussed. RECOMMENDATIONS All patients with nonsquamous NSCLC should have the results of testing for potentially targetable mutations (alterations) before implementing therapy for advanced lung cancer, regardless of smoking status recommendations, when possible, following other existing high-quality testing guidelines. Most patients should receive targeted therapy for these alterations: Targeted therapies against ROS-1 fusions, BRAF V600e mutations, RET fusions, MET exon 14 skipping mutations, and NTRK fusions should be offered to patients, either as initial or second-line therapy when not given in the first-line setting. New or revised recommendations include the following: Osimertinib is the optimal first-line treatment for patients with activating epidermal growth factor receptor mutations (exon 19 deletion, exon 21 L858R, and exon 20 T790M); alectinib or brigatinib is the optimal first-line treatment for patients with anaplastic lymphoma kinase fusions. For the first time, to our knowledge, the guideline includes recommendations regarding RET, MET, and NTRK alterations. Chemotherapy is still an option at most stages.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available