Publication

Resection following concurrent chemotherapy and high-dose radiation for stage IIIA non-small cell lung cancer

Downloadable Content

Persistent URL
Last modified
  • 09/12/2025
Type of Material
Authors
    Jessica S Donington, NYU School of MedicineRebecca Paulus, NRG Oncology Statistics and Data Management CenterMartin J Edelman, University of MarylandMark J Krasna, Jersey Shore University Medical CenterQuynh-Thu Le, Stanford Cancer InstituteMohan Suntharalingam, University of MarylandBilly W Loo, Stanford Cancer InstituteChen Hu, NRG Oncology Statistics and Data Management CenterJeffrey Bradley, Emory University
Language
  • English
Date
  • 2020-11-01
Publisher
  • MOSBY-ELSEVIER
Publication Version
Copyright Statement
  • © 2020 Published by Elsevier Inc. on behalf of The American Association for Thoracic Surgery
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 160
Issue
  • 5
Start Page
  • 1331
End Page
  • +
Grant/Funding Information
  • This project was supported by grants U10CA180868 (NRG Oncology Operations), U10CA180822 (NRG Oncology SDMC), U24CA180803 (IROC) from the National Cancer Institute (NCI) and Amgen.
Supplemental Material (URL)
Abstract
  • Objective: Concern exists regarding surgery after thoracic radiation. We aimed to assess early results of anatomic resection following induction therapy with platinum-based chemotherapy and full-dose thoracic radiation for resectable N2+ stage IIIA non–small cell lung cancer. Methods: Two prospective trials were recently conducted by NRG Oncology in patients with resectable N2+ stage IIIA non–small cell lung cancer with the primary end point of mediastinal node sterilization following concurrent full-dose chemoradiotherapy (Radiation Therapy Oncology Group trials 0229 and 0839). All surgeons demonstrated postinduction resection expertise. Induction consisted of weekly carboplatin (area under the curve, 2.0) and paclitaxel (50 mg/m2) and concurrent thoracic radiation 60 Gy (0839)/61.2 Gy (0229) in 30 fractions. Patients in study 0839 were randomized 2:1 to weekly panitumumab + chemoradiotherapy or chemoradiotherapy alone during induction. Primary results were similar in all treatment arms and reported previously. Short-term surgical outcomes are reported here. Results: One hundred twenty-six patients enrolled; 93 (74%) had anatomic resection, 77 underwent lobectomy, and 16 underwent extended resection. Microscopically margin-negative resections occurred in 85 (91%). Fourteen (15%) resections were attempted minimally invasively, including 2 converted without event. Grade 3 or 4 surgical adverse events were reported in 26 (28%), 30-day mortality in 4 (4%) and 90-day mortality in 5 (5%). Patients undergoing extended resection experienced similar rates of grade 3 or 4 adverse events (odds ratio, 0.95; 95% confidence interval, 0.42-3.8) but higher 30-day (1.3% vs 18.8%) (odds ratio, 17.54; 95% confidence interval, 1.75-181.8) and 90-day mortality (2.6% vs 18.8%) (odds ratio, 8.65; 95% confidence interval, 1.3-56.9). Conclusions: Lobectomy was performed safely following full-dose concurrent chemoradiotherapy in these multi-institutional prospective trials; however, increased mortality was noted with extended resections.
Author Notes
  • Jessica S. Donington, MD, MSCR, Professor and Chief, Thoracic Surgery, University of Chicago Medicine, 5758 S. Maryland Ave, Suite S500, Chicago, IL 60637, 773-702-3551. Email: jdonington@uchicago.edu
Keywords
Research Categories
  • Statistics

Tools

Relations

In Collection:

Items