Therapy for Stage IV Non–Small-Cell Lung Cancer Without Driver Alterations: ASCO Living Guideline

Author:

Singh Navneet1ORCID,Temin Sarah2ORCID,Baker Sherman3,Blanchard Elizabeth4,Brahmer Julie R.5ORCID,Celano Paul6,Duma Narjust7ORCID,Ellis Peter M.8,Elkins Ivy B.9,Haddad Rami Y.10,Hesketh Paul J.11ORCID,Jain Dharamvir12,Johnson David H.13ORCID,Leighl Natasha B.14ORCID,Mamdani Hirva15ORCID,Masters Gregory16ORCID,Moffitt Pamela R.17,Phillips Tanyanika18,Riely Gregory J.19ORCID,Robinson Andrew G.20ORCID,Rosell Rafael21ORCID,Schiller Joan H.22ORCID,Schneider Bryan J.23,Spigel David R.24ORCID,Jaiyesimi Ishmael A.25

Affiliation:

1. Postgraduate Institute of Medical Education and Research, Chandigarh, India

2. American Society of Clinical Oncology, Alexandria, VA

3. Virginia Commonwealth University, Richmond, VA

4. Southcoast Centers for Cancer Care, New Bedford, MA

5. Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD

6. The Cancer Center at GBMC, Townson, MD

7. Dana-Farber Cancer Institute, Boston, MA

8. Juravinski Cancer Centre, Hamilton, Ontario, Canada

9. EGFR Resisters, Buffalo Grove, IL

10. Affiliated Oncologists, LLC, Chicago Ridge, IL

11. Lahey Hospital and Medical Center, Burlington, MA

12. Houston Methodist Cancer Center, Houston, TX

13. University of Texas Southwestern Medical Center, Dallas, TX

14. Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada

15. Karmanos Cancer Institute/Wayne State University, Detroit, MI

16. Helen F. Graham Cancer Center and Research Institute, Newark, DE

17. Patient Advocate, Galva, IA

18. City of Hope, Duarte, CA

19. Memorial Sloan Kettering Cancer Center, New York, NY

20. Kingston General Hospital, Queen's University, Ontario, Canada

21. Catalan Institute of Oncology, Barcelona, Catalonia, Spain

22. Inova Schar Cancer Institute, Falls Church, VA

23. University of Michigan Health System, Ann Arbor, MI

24. Sarah Cannon Research Institute, Nashville, TN

25. Beaumont Health Royal Oak and Oakland University William Beaumont School of Medicine, Royal Oak, MI

Abstract

Living guidelines are routinely updated guidelines that are developed for selected topic areas with rapidly evolving evidence that drives frequent change in clinical practice. These guidelines are updated on a regular schedule, based on the work of a standing panel that reviews the literature on a continuous basis. Updates will be made regularly and can be found at https://ascopubs.org/nsclc-non-da-living-guideline . PURPOSE To provide evidence-based recommendations updating the 2020 ASCO and Ontario Health (Cancer Care Ontario) guideline on systemic therapy for patients with stage IV non–small-cell lung cancer without driver alterations. METHODS ASCO updated recommendations on the basis of an ongoing systematic review of randomized clinical trials from 2018 to 2021. RESULTS This guideline update reflects changes in evidence since the previous update. Five randomized clinical trials provide the evidence base. Outcomes of interest include efficacy and safety. RECOMMENDATIONS In addition to 2020 options for patients with high programmed death ligand-1 (PD-L1) expression (tumor proportion score [TPS] ≥ 50%), nonsquamous cell carcinoma (non-SCC), and performance status (PS) 0-1, clinicians may offer single-agent atezolizumab. With high PD-L1 expression (TPS ≥ 50%), non-SCC, and PS 0-1, clinicians may offer nivolumab and ipilumumab alone or nivolumab and ipilimumab plus chemotherapy. With negative (0%) and low positive PD-L1 expression (TPS 1%-49%), non-SCC, and PS 0-1, clinicians may offer nivolumab and ipilimumab alone or nivolumab and ipilimumab plus chemotherapy. With high PD-L1 expression, SCC, and PS 0-1, clinicians may offer single-agent atezolizumab. With high PD-L1 expression, squamous cell carcinoma (SCC), and PS 0-1, clinicians may offer nivolumab and ipilimumab alone or in combination with two cycles of platinum-based chemotherapy. With negative and low positive PD-L1 expression, SCC, and PS 0-1, clinicians may offer nivolumab and ipilimumab alone or in combination with two cycles of platinum-based chemotherapy. With non-SCC who received an immune checkpoint inhibitor and chemotherapy as first-line therapy, clinicians may offer second-line paclitaxel plus bevacizumab. With non-SCC, who received chemotherapy with or without bevacizumab and immune checkpoint inhibitor therapy, clinicians should offer the options of third-line single-agent pemetrexed, docetaxel, or paclitaxel plus bevacizumab. Additional information is available at www.asco.org/thoracic-cancer-guidelines .

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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