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

  • NRG Oncology Lung Group
  • University of Chicago
  • New York University
  • NRG Oncology Statistics and Data Management Center
  • Radiation Therapy Oncology Group Statistical Center
  • Jersey Shore University Medical Center
  • University of Maryland Cancer Center
  • Cancer Center at St. Joseph Medical Center
  • University of Maryland
  • Stanford University
  • Southwest Oncology Group
  • University of Maryland Medical System
  • Mayo Clinic
  • Johns Hopkins University
  • Washington University St. Louis
  • Emory University
  • University of Bern
  • Clark Atlanta University
  • University of Pennsylvania

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

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.

Original languageEnglish
Pages (from-to)1331-1345.e1
JournalJournal of Thoracic and Cardiovascular Surgery
Volume160
Issue number5
DOIs
StatePublished - Nov 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adult
  • Aged
  • Antineoplastic Agents/adverse effects
  • Carcinoma, Non-Small-Cell Lung/pathology
  • Chemoradiotherapy/adverse effects
  • Female
  • Humans
  • Lung Neoplasms/pathology
  • Male
  • Middle Aged
  • Pneumonectomy/adverse effects
  • Postoperative Complications/epidemiology
  • Retrospective Studies

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