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Poster Display session 1

5315 - Whole brain radiotherapy plus simultaneous in-field boost versus whole brain radiotherapy plus fractionated stereotactic radiotherapy for multiple brain metastases of non-small cell lung cancer


28 Sep 2019


Poster Display session 1


Tumour Site

Non-Small Cell Lung Cancer;  Central Nervous System Malignancies


Lu Li


Annals of Oncology (2019) 30 (suppl_5): v143-v158. 10.1093/annonc/mdz243


L. Li1, M. feng2, P. xu2, J. Yin2, Y. Huang2, X. Peng3, J. lang2

Author affiliations

  • 1 School Of Medicine,university Of Electronic Science And Technology, Sichuan Cancer Hospital, 610041 - Chengdu/CN
  • 2 Radiation Oncology, sichuan cancer hospital, 610000 - chengdu/CN
  • 3 Radiation Oncology, Guangxi Medical University, 530021 - nanning/CN


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Abstract 5315


Brain metastasis (BM) is common among patients with non-small cell lung cancer (NSCLC). Whole brain radiotherapy (WBRT) plus a radiation boost is a common treatment strategy for such patients. WBRT plus simultaneous in-field boost (WBRT+SIB) and WBRT plus hypo-fractionated stereotactic radiotherapy (WBRT+FSRT) have shown promising outcomes. The current study compared the efficacy and safety of these two treatment strategies.


Sixty-six NSCLC patients with multiple BMs who met the inclusion criteria from January 2010 to December 2016 were enrolled. The efficacy and toxicity of WBRT+SIB and WBRT+FSRT were analyzed retrospectively. A Cox proportional hazard model was used to identify prognostic factors.


The objective response rates in the WBRT+SIB and WBRT+FSRT groups were similar (74.9% and 79.4%, respectively; p = 0.5), as was the disease control rate (93.8% and 97.1%, respectively; P = 0.3). The median survival time was 15.3 months in the WBRT+SIB group and 25.2 months in the WBRT+FSRT group (p = 0.02). The median local progression-free survival was 13 months in the WBRT+SIB group and 17 months in the WBRT+FSRT group (p = 0.04). The incidence of 1-3 grade toxicity was slightly lower in the WBRT+FSRT group than the WBRT+SIB group (31.2% vs. 38.2%). Compared to the WBRT+SIB group, the WBRT+FSRT group was associated with a lower risk of mortality (HR = 0.6; 95% CI, 0.1-0.7) in the Cox multivariate model. Extracranial metastases, worse recursive partitioning analysis class, and non-surgical treatment of primary lesions were associated with a worse prognosis.


Compared to WBRT+SIB, WBRT+FSRT treatment was associated with a better prognosis and slightly less toxicity in patients with multiple BMs from NSCLC. Further studies are warranted to better elucidate the difference and determine the optimal dose/fractionation.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Jinyi Lang.


Has not received any funding.


All authors have declared no conflicts of interest.

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