Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2021 May;22(3):225-233.e7.
doi: 10.1016/j.cllc.2020.06.018. Epub 2020 Jun 28.

Postoperative Radiotherapy for Locally Advanced NSCLC: Implications for Shifting to Conformal, High-Risk Fields

Affiliations
Comparative Study

Postoperative Radiotherapy for Locally Advanced NSCLC: Implications for Shifting to Conformal, High-Risk Fields

Bhavana V Chapman et al. Clin Lung Cancer. 2021 May.

Abstract

Background: To examine the effect of radiotherapy field size on survival outcomes and patterns of recurrence in patients treated with postoperative radiotherapy (PORT) for non-small-cell lung cancer (NSCLC).

Methods: We retrospectively reviewed the records of 216 patients with T1-4 N1-2 NSCLC following surgery and PORT using whole mediastinum (WM) or high-risk (HR) nodal fields from 1998 to 2015. Survival rates were calculated using the Kaplan-Meier method. Univariate and multivariable analyses were conducted using Cox proportional hazards modeling for outcomes and logistic regression analysis for treatment toxicities.

Results: Median follow-up was 28 months (interquartile range [IQR] 13-75 months) and 38 months (IQR 19-73 months) for WM (n = 131) and HR (n = 84) groups, respectively. Overall survival (OS) was not significantly different between groups (median OS: HR 49 vs. WM 32 months; P = .08). There was no difference in progression-free survival (PFS), freedom from locoregional recurrence (LRR), or freedom from distant metastasis (P > .2 for all). Field size was not associated with OS, PFS, or LRR (P > .40 for all). LRR rates were 20% for HR and 26% for WM groups (P = .30). There was no significant difference in patterns of initial site of LRR between groups (P > .1). WM fields (OR 3.73, P = .001) and concurrent chemotherapy (odds ratio 3.62, P = .001) were associated with grade ≥2 toxicity.

Conclusions: Locoregional control and survival rates were similar between PORT groups; an improved toxicity profile was observed in the HR group. Results from an ongoing prospective randomized clinical trial will provide further insight into the consequences of HR PORT fields.

Keywords: Locoregional control; Non–small-cell lung cancer; PORT; Patterns of recurrence; Toxicity.

PubMed Disclaimer

Conflict of interest statement

Conflicts of Interest

The authors report no conflicts of interest relevant to this work. S.M. reports personal fees from Oscar Health, outside the submitted work. S.H.L. reports grants from Hitachi Chemical Diagnostics and Genentech, grants and personal fees from Beyond Spring Pharmaceuticals, personal fees from AstraZeneca and Varian Medical Systems, all outside the submitted work. C.T. reports personal fees from Reflexion, AstraZeneca, and Wolter Kluwer, all outside the submitted work. In addition, C.T. holds a patent U.S. Patent (patent #9,175,079) licensed to The Board of Trustees of the Leland Stanford Junior University. J.Y.C. reports grants from BMS, personal fees from Varian Medical System and AstraZeneca, and shareholdings from Global Oncology One, all outside the submitted work. S.J.G. reports grants from Bristol Myers Squibb and Astrazeneca, and personal fees from Novocure Scientific Advisory Board, all outside the submitted work. D.R.G. reports grants and personal fees from Bristol-Myers Squibb, Varian, AstraZeneca, and Merck, personal fees from Vindico, Medscape, and Reflexion, all outside the submitted work.

Figures

Figure 1:
Figure 1:
Representative A) whole mediastinum field and B) high-risk field.
Figure 2:
Figure 2:
A) Overall survival (OS), B) Progression-free survival (PFS), C) Freedom from locoregional recurrence-free survival (FFLRR), and D) Freedom from distant metastasis (FFDM) according to field size.

References

    1. Lally BE, Zelterman D, Colasanto JM, Haffty BG, Detterbeck FC, Wilson LD. Postoperative radiotherapy for stage II or III non-small-cell lung cancer using the surveillance, epidemiology, and end results database. J Clin Oncol. 2006;24(19):2998–3006. 10.1200/JCO.2005.04.6110 - DOI - PubMed
    1. Douillard J-Y, Rosell R, De Lena M, et al. Impact of postoperative radiation therapy on survival in patients with complete resection and stage I, II, or IIIA non-small-cell lung cancer treated with adjuvant chemotherapy: the adjuvant Navelbine International Trialist Association (ANITA) Randomized Trial. Int J Radiat Oncol Biol Phys. 2008;72(3):695–701. 10.1016/j.ijrobp.2008.01.044 - DOI - PubMed
    1. PORT Meta-analysis Trialists Group. Postoperative radiotherapy for non-small cell lung cancer. Cochrane Database Syst Rev. 2005;(2):CD002142. 10.1002/14651858.CD002142.pub2 - DOI - PubMed
    1. Lee JH, Machtay M, Kaiser LR, et al. Non-small cell lung cancer: prognostic factors in patients treated with surgery and postoperative radiation therapy. Radiology. 1999;213(3):845–852. 10.1148/radiology.213.3.r99dc23845 - DOI - PubMed
    1. Feng QF, Wang M, Wang LJ, et al. A study of postoperative radiotherapy in patients with non-small-cell lung cancer: a randomized trial. Int J Radiat Oncol Biol Phys. 2000;47(4):925–929. 10.1016/s0360-3016(00)00509-5 - DOI - PubMed

Publication types