Literature DB >> 33591844

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

Nasser H Hanna1, Andrew G Robinson2, Sarah Temin3, Sherman Baker4, Julie R Brahmer5, Peter M Ellis6, Laurie E Gaspar7,8, Rami Y Haddad9, Paul J Hesketh10, Dharamvir Jain11, Ishmael Jaiyesimi12, David H Johnson13, Natasha B Leighl14, Pamela R Moffitt15, Tanyanika Phillips16, Gregory J Riely17, Rafael Rosell18, Joan H Schiller19, Bryan J Schneider20, Navneet Singh21, David R Spigel22, Joan Tashbar23, Gregory Masters24.   

Abstract

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.Additional information is available at www.asco.org/thoracic-cancer-guidelines.

Entities:  

Year:  2021        PMID: 33591844     DOI: 10.1200/JCO.20.03570

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  51 in total

1.  Impact of previous corticosteroid exposure on outcomes of patients receiving immune checkpoint inhibitors for advanced non-small cell lung cancer: a retrospective observational study.

Authors:  F Nelli; A Virtuoso; J R Giron Berrios; D Giannarelli; A Fabbri; E Marrucci; E M Ruggeri
Journal:  Cancer Chemother Pharmacol       Date:  2022-03-18       Impact factor: 3.333

Review 2.  Aumolertinib: A Review in Non-Small Cell Lung Cancer.

Authors:  Matt Shirley; Susan J Keam
Journal:  Drugs       Date:  2022-03-19       Impact factor: 9.546

3.  Prognosis of different extrathoracic metastasis patterns in patients with M1c lung adenocarcinoma receiving immunotherapy.

Authors:  Fang Hu; Jin Peng; Xiaowei Mao; Yanjie Niu; Meili Ma; Yizhuo Zhao; Aiqin Gu; Liyan Jiang
Journal:  J Cancer Res Clin Oncol       Date:  2022-07-27       Impact factor: 4.322

4.  Targeting Anaplastic Lymphoma Kinase in GI Primary Malignancies.

Authors:  Jerold Loh; Yvonne Li En Ang; Amit Jain; Joe Yeong; Raghav Sundar
Journal:  JCO Precis Oncol       Date:  2022-07

5.  Setting Up an Ultra-Fast Next-Generation Sequencing Approach as Reflex Testing at Diagnosis of Non-Squamous Non-Small Cell Lung Cancer; Experience of a Single Center (LPCE, Nice, France).

Authors:  Marius Ilié; Véronique Hofman; Christophe Bontoux; Simon Heeke; Virginie Lespinet-Fabre; Olivier Bordone; Sandra Lassalle; Salomé Lalvée; Virginie Tanga; Maryline Allegra; Myriam Salah; Doriane Bohly; Jonathan Benzaquen; Charles-Hugo Marquette; Elodie Long-Mira; Paul Hofman
Journal:  Cancers (Basel)       Date:  2022-04-30       Impact factor: 6.575

6.  Concordance Between Tissue ALK Detection by Immunohistochemistry and Plasma ALK Detection by Next-Generation Sequencing in the Randomized Phase 3 ALEX Study in Patients With Treatment-Naive Advanced ALK-Positive NSCLC.

Authors:  Johannes Noé; Walter Bordogna; Venice Archer; Vlatka Smoljanovic; Magalie Hilton; Ryan Woodhouse; Simonetta Mocci; Shirish M Gadgeel
Journal:  JTO Clin Res Rep       Date:  2022-05-18

Review 7.  Crosstalk between the B7/CD28 and EGFR pathways: Mechanisms and therapeutic opportunities.

Authors:  Xiaoxin Ren; Yixian Li; Christopher Nishimura; Xingxing Zang
Journal:  Genes Dis       Date:  2021-09-20

8.  A Phase 1, Open-Label, Dose-Escalation Study of L-DOS47 in Combination With Pemetrexed Plus Carboplatin in Patients With Stage IV Recurrent or Metastatic Nonsquamous NSCLC.

Authors:  Sarina Piha-Paul; George Simon; Chandra P Belani; Heman Chao; Kim Gaspar; Brenda Lee; Afshin Dowlati
Journal:  JTO Clin Res Rep       Date:  2022-09-16

Review 9.  Targeted therapy for advanced anaplastic lymphoma kinase (<I>ALK</I>)-rearranged non-small cell lung cancer.

Authors:  Laird B Cameron; Nadia Hitchen; Elias Chandran; Tessa Morris; Renée Manser; Benjamin J Solomon; Vanessa Jordan
Journal:  Cochrane Database Syst Rev       Date:  2022-01-07

10.  Meningeal "Lazarus Response" to Lorlatinib in a ROS1-Positive NSCLC Patient Progressing to Entrectinib.

Authors:  Francesco Facchinetti; Antonin Levy; Samy Ammari; Charles Naltet; Pernelle Lavaud; Mihaela Aldea; Damien Vasseur; David Planchard; Benjamin Besse
Journal:  Cancer Manag Res       Date:  2021-03-26       Impact factor: 3.989

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