» Articles » PMID: 27502703

Improved Survival with Dose-escalated Radiotherapy in Stage III Non-small-cell Lung Cancer: Analysis of the National Cancer Database

Overview
Journal Ann Oncol
Publisher Elsevier
Specialty Oncology
Date 2016 Aug 10
PMID 27502703
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Concurrent chemoradiation is the standard of care in non-operable stage III non-small-cell lung cancer (NSCLC). Data have suggested a benefit of dose escalation; however, results from the randomized dose-escalation trial RTOG 0617 revealed a lower survival rate with high-dose radiation. To evaluate the impact of dose escalation on overall survival (OS) in stage III NSCLC treated with chemoradiotherapy outside the controlled setting of a randomized trial, we carried out an observational, population-based investigation of the National Cancer Database (NCDB).

Patients And Methods: A total of 33 566 patients with stage III NSCLC treated with chemoradiation from 2004 to 2012 and radiation doses between 59.4 and 85 Gy were included. The primary end point was OS, with median survival calculated via Kaplan-Meier. Univariate, multivariable and propensity-score matching analyses were carried out.

Results: Patients were stratified by dose with median OS of: 18.8, 19.8 and 21.6 months for cohorts receiving 59.4-60, 61-69 and ≥70 Gy, respectively (P < 0.001). Granular dose analyses were carried out demonstrating increased OS with increasing radiation dose: median survival of 18.8, 21.1, 22.0 and 21.0 months for 59.4-60, 66, 70 and ≥71 Gy, respectively. While 66, 70 and ≥71 Gy resulted in increased OS in comparison with 59.4-60 Gy, no significant difference in OS was observed when comparing 66 with ≥71 Gy (P = 0.38).

Conclusions: Dose escalation above 60 Gy was associated with improved OS in this cohort of stage III NSCLC patients treated with chemoradiotherapy. A plateau of benefit was observed, with no additional improvement in OS with increased dose (≥71 Gy) compared with 66-70 Gy. With evidence suggesting worse OS and quality of life with increased dose, these data support investigation of the role of intermediate-dose radiation, and in the absence of randomized evidence, may be leveraged to justify utilization of intermediate-dose radiation.

Citing Articles

Treatment of non-small cell lung cancer: advances following the introduction of PET-CT and IMRT/VMAT.

Muster J, Alt N, Edelmann M, Anczykowski M, Zwerenz C, Schirmer M Strahlenther Onkol. 2025; .

PMID: 40050448 DOI: 10.1007/s00066-025-02377-0.


High radiation dose in chemoradiotherapy followed by immunotherapy with durvalumab in patients with stage III non-small cell lung cancer does not increase risk for pneumonitis.

Schragel F, Matousek M, Resl C, Kreye G, Le N, Errhalt P Strahlenther Onkol. 2025; .

PMID: 39945842 DOI: 10.1007/s00066-025-02369-0.


Efficacies of different postoperative radiotherapy techniques in patients with N2 non-small cell lung cancer: a meta-analysis.

Yao B, Zhang H, Liang X, Zhao T, Hu J, Ge J Am J Transl Res. 2024; 16(11):7016-7035.

PMID: 39678624 PMC: 11645576. DOI: 10.62347/JGIB9696.


Long-term outcome of definitive radiotherapy for locally advanced non-small cell lung cancer: A real-world single-center study in the pre-durvalumab era.

Zhu H, Xu Y, Gao H, Fan X, Fan M, Zhao K Cancer Med. 2024; 13(15):e70051.

PMID: 39082888 PMC: 11289899. DOI: 10.1002/cam4.70051.


Feasibility of Four-dimensional Adaptation of Volumetric Modulated Arc Therapy Based on Volumetric Modulated Arc Therapy-computed Tomography.

Zhao X, Zhang R J Med Phys. 2023; 48(2):154-160.

PMID: 37576092 PMC: 10419754. DOI: 10.4103/jmp.jmp_24_23.