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


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 10 2022
Historique:
pubmed: 12 7 2022
medline: 1 10 2022
entrez: 11 7 2022
Statut: ppublish

Résumé

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. ASCO updated recommendations on the basis of an ongoing systematic review of randomized clinical trials from 2018 to 2021. 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. 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.

Identifiants

pubmed: 35816668
doi: 10.1200/JCO.22.00825
doi:

Substances chimiques

B7-H1 Antigen 0
Immune Checkpoint Inhibitors 0
Ipilimumab 0
Pemetrexed 04Q9AIZ7NO
Docetaxel 15H5577CQD
Bevacizumab 2S9ZZM9Q9V
Nivolumab 31YO63LBSN
Paclitaxel P88XT4IS4D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3323-3343

Commentaires et corrections

Type : UpdateIn
Type : UpdateIn
Type : UpdateIn

Auteurs

Navneet Singh (N)

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

Sarah Temin (S)

American Society of Clinical Oncology, Alexandria, VA.

Sherman Baker (S)

Virginia Commonwealth University, Richmond, VA.

Elizabeth Blanchard (E)

Southcoast Centers for Cancer Care, New Bedford, MA.

Julie R Brahmer (JR)

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

Paul Celano (P)

The Cancer Center at GBMC, Townson, MD.

Narjust Duma (N)

Dana-Farber Cancer Institute, Boston, MA.

Peter M Ellis (PM)

Juravinski Cancer Centre, Hamilton, Ontario, Canada.

Ivy B Elkins (IB)

EGFR Resisters, Buffalo Grove, IL.

Rami Y Haddad (RY)

Affiliated Oncologists, LLC, Chicago Ridge, IL.

Paul J Hesketh (PJ)

Lahey Hospital and Medical Center, Burlington, MA.

Dharamvir Jain (D)

Houston Methodist Cancer Center, Houston, TX.

David H Johnson (DH)

University of Texas Southwestern Medical Center, Dallas, TX.

Natasha B Leighl (NB)

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

Hirva Mamdani (H)

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

Gregory Masters (G)

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

Pamela R Moffitt (PR)

Patient Advocate, Galva, IA.

Tanyanika Phillips (T)

City of Hope, Duarte, CA.

Gregory J Riely (GJ)

Memorial Sloan Kettering Cancer Center, New York, NY.

Andrew G Robinson (AG)

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

Rafael Rosell (R)

Catalan Institute of Oncology, Barcelona, Catalonia, Spain.

Joan H Schiller (JH)

Inova Schar Cancer Institute, Falls Church, VA.

Bryan J Schneider (BJ)

University of Michigan Health System, Ann Arbor, MI.

David R Spigel (DR)

Sarah Cannon Research Institute, Nashville, TN.

Ishmael A Jaiyesimi (IA)

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

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH