Stereotactic body radiation therapy for early-stage non-small cell lung cancer: Executive Summary of an ASTRO Evidence-Based Guideline.

Published

Journal Article

This guideline presents evidence-based recommendations for stereotactic body radiation therapy (SBRT) in challenging clinical scenarios in early-stage non-small cell lung cancer (NSCLC).The American Society for Radiation Oncology convened a task force to perform a systematic literature review on 4 key questions addressing: (1) application of SBRT to operable patients; (2) appropriate use of SBRT in tumors that are centrally located, large, multifocal, or unbiopsied; (3) individual tailoring of SBRT in "high-risk" clinical scenarios; and (4) SBRT as salvage therapy after recurrence. Guideline recommendations were created using a predefined consensus-building methodology supported by American Society for Radiation Oncology-approved tools for grading evidence quality and recommendation strength.Although few randomized trials have been completed for SBRT, strong consensus recommendations based on extensive, consistent publications were generated for several questions, including recommendations for fractionation for central tumors and surgery versus SBRT in standard-risk medically operable patients with early-stage NSCLC. Lower quality evidence led to conditional recommendations on use of SBRT for tumors >5 cm, patients with prior pneumonectomy, T3 tumors with chest wall invasion, synchronous multiple primary lung cancer, and as a salvage therapy after prior radiation therapy. These areas of moderate- and low-quality evidence highlight the importance of clinical trial enrollment as well as the role of prospective data registries.SBRT has an important role to play in treating early-stage NSCLC, particularly for medically inoperable patients with limited other treatment options. Shared decision-making with patients should be performed in all cases to ensure the patient understands the risks related to SBRT, the side effects, and the alternative treatments available.

Full Text

Duke Authors

Cited Authors

  • Videtic, GMM; Donington, J; Giuliani, M; Heinzerling, J; Karas, TZ; Kelsey, CR; Lally, BE; Latzka, K; Lo, SS; Moghanaki, D; Movsas, B; Rimner, A; Roach, M; Rodrigues, G; Shirvani, SM; Simone, CB; Timmerman, R; Daly, ME

Published Date

  • September 2017

Published In

Volume / Issue

  • 7 / 5

Start / End Page

  • 295 - 301

PubMed ID

  • 28596092

Pubmed Central ID

  • 28596092

Electronic International Standard Serial Number (EISSN)

  • 1879-8519

International Standard Serial Number (ISSN)

  • 1879-8500

Digital Object Identifier (DOI)

  • 10.1016/j.prro.2017.04.014

Language

  • eng