Therapy for Stage IV Non-Small-Cell Lung Cancer Without Driver Alterations: ASCO and OH (CCO) Joint Guideline Update
The aim of this work is to provide evidence-based recommendations updating the 2017 ASCO guideline on systemic therapy for patients with stage IV non-small-cell lung cancer (NSCLC) without driver alterations. A guideline update for patients with stage IV NSCLC with driver alterations will be publish...
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| Published in: | Journal of clinical oncology Vol. 38; no. 14; p. 1608 |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
United States
10.05.2020
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| Subjects: | |
| ISSN: | 1527-7755, 1527-7755 |
| Online Access: | Get more information |
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| Abstract | The aim of this work is to provide evidence-based recommendations updating the 2017 ASCO guideline on systemic therapy for patients with stage IV non-small-cell lung cancer (NSCLC) without driver alterations. A guideline update for patients with stage IV NSCLC with driver alterations will be published separately.
The American Society of Clinical Oncology and Ontario Health (Cancer Care Ontario) NSCLC Expert Panel made updated recommendations based on a systematic review of randomized controlled trials from December 2015 to 2019.
This guideline update reflects changes in evidence since the previous guideline update. Five randomized controlled trials provide the evidence base. Additional literature suggested by the Expert Panel is discussed.
Recommendations apply to patients without driver alterations in epidermal growth factor receptor or ALK. For patients with high programmed death ligand 1 (PD-L1) expression (tumor proportion score [TPS] ≥ 50%) and non-squamous cell carcinoma (non-SCC), the Expert Panel recommends single-agent pembrolizumab. Additional treatment options include pembrolizumab/carboplatin/pemetrexed, atezolizumab/carboplatin/paclitaxel/bevacizumab, or atezolizumab/carboplatin/nab-paclitaxel. For most patients with non-SCC and either negative (0%) or low positive (1% to 49%) PD-L1, the Expert Panel recommends pembrolizumab/carboplatin/pemetrexed. Additional options are atezolizumab/carboplatin/nab-paclitaxel, atezolizumab/carboplatin/paclitaxel/bevacizumab, platinum-based two-drug combination chemotherapy, or non-platinum-based two-drug therapy. Single-agent pembrolizumab is an option for low positive PD-L1. For patients with high PD-L1 expression (TPS ≥ 50%) and SCC, the Expert Panel recommends single-agent pembrolizumab. An additional treatment option is pembrolizumab/carboplatin/(paclitaxel or nab-paclitaxel). For most patients with SCC and either negative (0%) or low positive PD-L1 (TPS 1% to 49%), the Expert Panel recommends pembrolizumab/carboplatin/(paclitaxel or nab-paclitaxel) or chemotherapy. Single-agent pembrolizumab is an option in select cases of low positive PD-L1. Recommendations are conditional on the basis of histology, PD-L1 status, and/or the presence or absence of contraindications. Additional information is available at www.asco.org/lung-cancer-guidelines. |
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| AbstractList | The aim of this work is to provide evidence-based recommendations updating the 2017 ASCO guideline on systemic therapy for patients with stage IV non-small-cell lung cancer (NSCLC) without driver alterations. A guideline update for patients with stage IV NSCLC with driver alterations will be published separately.PURPOSEThe aim of this work is to provide evidence-based recommendations updating the 2017 ASCO guideline on systemic therapy for patients with stage IV non-small-cell lung cancer (NSCLC) without driver alterations. A guideline update for patients with stage IV NSCLC with driver alterations will be published separately.The American Society of Clinical Oncology and Ontario Health (Cancer Care Ontario) NSCLC Expert Panel made updated recommendations based on a systematic review of randomized controlled trials from December 2015 to 2019.METHODSThe American Society of Clinical Oncology and Ontario Health (Cancer Care Ontario) NSCLC Expert Panel made updated recommendations based on a systematic review of randomized controlled trials from December 2015 to 2019.This guideline update reflects changes in evidence since the previous guideline update. Five randomized controlled trials provide the evidence base. Additional literature suggested by the Expert Panel is discussed.RESULTSThis guideline update reflects changes in evidence since the previous guideline update. Five randomized controlled trials provide the evidence base. Additional literature suggested by the Expert Panel is discussed.Recommendations apply to patients without driver alterations in epidermal growth factor receptor or ALK. For patients with high programmed death ligand 1 (PD-L1) expression (tumor proportion score [TPS] ≥ 50%) and non-squamous cell carcinoma (non-SCC), the Expert Panel recommends single-agent pembrolizumab. Additional treatment options include pembrolizumab/carboplatin/pemetrexed, atezolizumab/carboplatin/paclitaxel/bevacizumab, or atezolizumab/carboplatin/nab-paclitaxel. For most patients with non-SCC and either negative (0%) or low positive (1% to 49%) PD-L1, the Expert Panel recommends pembrolizumab/carboplatin/pemetrexed. Additional options are atezolizumab/carboplatin/nab-paclitaxel, atezolizumab/carboplatin/paclitaxel/bevacizumab, platinum-based two-drug combination chemotherapy, or non-platinum-based two-drug therapy. Single-agent pembrolizumab is an option for low positive PD-L1. For patients with high PD-L1 expression (TPS ≥ 50%) and SCC, the Expert Panel recommends single-agent pembrolizumab. An additional treatment option is pembrolizumab/carboplatin/(paclitaxel or nab-paclitaxel). For most patients with SCC and either negative (0%) or low positive PD-L1 (TPS 1% to 49%), the Expert Panel recommends pembrolizumab/carboplatin/(paclitaxel or nab-paclitaxel) or chemotherapy. Single-agent pembrolizumab is an option in select cases of low positive PD-L1. Recommendations are conditional on the basis of histology, PD-L1 status, and/or the presence or absence of contraindications. Additional information is available at www.asco.org/lung-cancer-guidelines.RECOMMENDATIONSRecommendations apply to patients without driver alterations in epidermal growth factor receptor or ALK. For patients with high programmed death ligand 1 (PD-L1) expression (tumor proportion score [TPS] ≥ 50%) and non-squamous cell carcinoma (non-SCC), the Expert Panel recommends single-agent pembrolizumab. Additional treatment options include pembrolizumab/carboplatin/pemetrexed, atezolizumab/carboplatin/paclitaxel/bevacizumab, or atezolizumab/carboplatin/nab-paclitaxel. For most patients with non-SCC and either negative (0%) or low positive (1% to 49%) PD-L1, the Expert Panel recommends pembrolizumab/carboplatin/pemetrexed. Additional options are atezolizumab/carboplatin/nab-paclitaxel, atezolizumab/carboplatin/paclitaxel/bevacizumab, platinum-based two-drug combination chemotherapy, or non-platinum-based two-drug therapy. Single-agent pembrolizumab is an option for low positive PD-L1. For patients with high PD-L1 expression (TPS ≥ 50%) and SCC, the Expert Panel recommends single-agent pembrolizumab. An additional treatment option is pembrolizumab/carboplatin/(paclitaxel or nab-paclitaxel). For most patients with SCC and either negative (0%) or low positive PD-L1 (TPS 1% to 49%), the Expert Panel recommends pembrolizumab/carboplatin/(paclitaxel or nab-paclitaxel) or chemotherapy. Single-agent pembrolizumab is an option in select cases of low positive PD-L1. Recommendations are conditional on the basis of histology, PD-L1 status, and/or the presence or absence of contraindications. Additional information is available at www.asco.org/lung-cancer-guidelines. The aim of this work is to provide evidence-based recommendations updating the 2017 ASCO guideline on systemic therapy for patients with stage IV non-small-cell lung cancer (NSCLC) without driver alterations. A guideline update for patients with stage IV NSCLC with driver alterations will be published separately. The American Society of Clinical Oncology and Ontario Health (Cancer Care Ontario) NSCLC Expert Panel made updated recommendations based on a systematic review of randomized controlled trials from December 2015 to 2019. This guideline update reflects changes in evidence since the previous guideline update. Five randomized controlled trials provide the evidence base. Additional literature suggested by the Expert Panel is discussed. Recommendations apply to patients without driver alterations in epidermal growth factor receptor or ALK. For patients with high programmed death ligand 1 (PD-L1) expression (tumor proportion score [TPS] ≥ 50%) and non-squamous cell carcinoma (non-SCC), the Expert Panel recommends single-agent pembrolizumab. Additional treatment options include pembrolizumab/carboplatin/pemetrexed, atezolizumab/carboplatin/paclitaxel/bevacizumab, or atezolizumab/carboplatin/nab-paclitaxel. For most patients with non-SCC and either negative (0%) or low positive (1% to 49%) PD-L1, the Expert Panel recommends pembrolizumab/carboplatin/pemetrexed. Additional options are atezolizumab/carboplatin/nab-paclitaxel, atezolizumab/carboplatin/paclitaxel/bevacizumab, platinum-based two-drug combination chemotherapy, or non-platinum-based two-drug therapy. Single-agent pembrolizumab is an option for low positive PD-L1. For patients with high PD-L1 expression (TPS ≥ 50%) and SCC, the Expert Panel recommends single-agent pembrolizumab. An additional treatment option is pembrolizumab/carboplatin/(paclitaxel or nab-paclitaxel). For most patients with SCC and either negative (0%) or low positive PD-L1 (TPS 1% to 49%), the Expert Panel recommends pembrolizumab/carboplatin/(paclitaxel or nab-paclitaxel) or chemotherapy. Single-agent pembrolizumab is an option in select cases of low positive PD-L1. Recommendations are conditional on the basis of histology, PD-L1 status, and/or the presence or absence of contraindications. Additional information is available at www.asco.org/lung-cancer-guidelines. |
| Author | Singh, Navneet Stabler, Janis O Schiller, Joan H Brahmer, Julie Ellis, Peter M Hesketh, Paul J Hanna, Nasser H Schneider, Bryan J Spigel, David R Tashbar, Joan Jain, Dharamvir Baker, Jr, Sherman Haddad, Rami Y Jaiyesimi, Ishmael Leighl, Natasha B Rosell, Rafael Gaspar, Laurie E Riely, Gregory J Phillips, Tanyanika Robinson, Andrew G Johnson, David H Masters, Gregory Temin, Sarah |
| Author_xml | – sequence: 1 givenname: Nasser H surname: Hanna fullname: Hanna, Nasser H organization: Indiana University Simon Cancer Center, Indianapolis, IN – sequence: 2 givenname: Bryan J surname: Schneider fullname: Schneider, Bryan J organization: University of Michigan Health System, Ann Arbor, MI – sequence: 3 givenname: Sarah surname: Temin fullname: Temin, Sarah organization: American Society of Clinical Oncology, Alexandria, VA – sequence: 4 givenname: Sherman surname: Baker, Jr fullname: Baker, Jr, Sherman organization: Virginia Commonwealth University, Richmond, VA – sequence: 5 givenname: Julie surname: Brahmer fullname: Brahmer, Julie organization: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, Baltimore, MD – sequence: 6 givenname: Peter M surname: Ellis fullname: Ellis, Peter M organization: Juravinski Cancer Centre, Hamilton, Ontario, Canada – sequence: 7 givenname: Laurie E surname: Gaspar fullname: Gaspar, Laurie E organization: Banner MD Anderson Cancer Center, Greeley, CO – sequence: 8 givenname: Rami Y surname: Haddad fullname: Haddad, Rami Y organization: Affiliated Oncologists, Chicago Ridge, IL – sequence: 9 givenname: Paul J surname: Hesketh fullname: Hesketh, Paul J organization: Lahey Hospital and Medical Center, Burlington, MA – sequence: 10 givenname: Dharamvir surname: Jain fullname: Jain, Dharamvir organization: Norton Cancer Institute, Louisville, KY – sequence: 11 givenname: Ishmael surname: Jaiyesimi fullname: Jaiyesimi, Ishmael organization: William Beaumont Hospital, Royal Oak, MI – sequence: 12 givenname: David H surname: Johnson fullname: Johnson, David H organization: University of Texas Southwestern Medical Center, Dallas, TX – sequence: 13 givenname: Natasha B surname: Leighl fullname: Leighl, Natasha B organization: Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada – sequence: 14 givenname: Tanyanika surname: Phillips fullname: Phillips, Tanyanika organization: City of Hope, City of Duarte, CA – sequence: 15 givenname: Gregory J surname: Riely fullname: Riely, Gregory J organization: Memorial Sloan Kettering Cancer Center, New York, NY – sequence: 16 givenname: Andrew G surname: Robinson fullname: Robinson, Andrew G organization: Kingston General Hospital, School of Medicine, Queen's University, Ontario, Canada – sequence: 17 givenname: Rafael surname: Rosell fullname: Rosell, Rafael organization: Catalan Institute of Oncology, Barcelona, Spain – sequence: 18 givenname: Joan H surname: Schiller fullname: Schiller, Joan H organization: Inova Schar Cancer Institute, Falls Church, VA – sequence: 19 givenname: Navneet surname: Singh fullname: Singh, Navneet organization: Postgraduate Institute of Medical Education and Research, Chandigarh, India – sequence: 20 givenname: David R surname: Spigel fullname: Spigel, David R organization: Sarah Cannon Research Institute, Nashville, TN – sequence: 21 givenname: Janis O surname: Stabler fullname: Stabler, Janis O organization: Patient advocate – sequence: 22 givenname: Joan surname: Tashbar fullname: Tashbar, Joan organization: Circle of Hope for Cancer Research, St Cloud, FL – sequence: 23 givenname: Gregory surname: Masters fullname: Masters, Gregory organization: Helen F. Graham Cancer Center and Research Institute, Newark, DE |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31990617$$D View this record in MEDLINE/PubMed |
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| Title | Therapy for Stage IV Non-Small-Cell Lung Cancer Without Driver Alterations: ASCO and OH (CCO) Joint Guideline Update |
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