TY - JOUR
T1 - Prophylactic cranial irradiation for limited-stage small-cell lung cancer patients
T2 - secondary findings from the prospective randomized phase 3 CONVERT trial
AU - Levy, Antonin
AU - Le Péchoux, Cécile
AU - Mistry, Hitesh
AU - Martel-Lafay, Isabelle
AU - Bezjak, Andrea
AU - Lerouge, Delphine
AU - Padovani, Laetitia
AU - Taylor, Paul
AU - Faivre-Finn, Corinne
N1 - Copyright © 2018 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.
PY - 2019/2/1
Y1 - 2019/2/1
N2 - INTRODUCTION: The impact of the dose and fractionation of thoracic radiotherapy on the risk of developing brain metastasis (BM) has not been evaluated prospectively in LS-SCLC patients receiving prophylactic cerebral irradiation (PCI).METHODS: Data in patients treated with PCI from the CONVERT trial was analysed.RESULTS: 449/547 (82%) received PCI after completion of chemoradiotherapy. Baseline brain imaging consisted of CT-scan in 356/449 patients (79%) and MRI in 83/449 (18%) patients. PCI was delivered to 220/273 participants (81%) in the twice-daily (BD) group and 229/270 in the once-daily (OD) group (85%; p=0.49). Total median PCI dose was 25Gy in both BD and OD groups (p=0.74). In patients who received PCI, 75 (17%) developed BM (35 [8%] in OD and 40 [9%] in BD) and 173 (39%) other extracranial progression. In the univariate analysis, GTV was associated with an increased risk of BM (p=0.007) or other radiological progression events (p=0.006), whereas in a multivariate analysis both thoracic GTV (tGTV) and PS were associated with either progression type. The median OS of patients treated with PCI was 29 months. In the univariate analysis of OS, PCI timing from end of chemotherapy, weight loss >10%, and tGTV were prognostic factors associated with OS. In the multivariate analysis, only tGTV was associated with OS. Delay between end of chemotherapy and PCI was not associated with OS.CONCLUSION: Patients receiving OD or BD thoracic RT have the same risk of developing BM. Larger tumours are associated with a higher risk of BM.
AB - INTRODUCTION: The impact of the dose and fractionation of thoracic radiotherapy on the risk of developing brain metastasis (BM) has not been evaluated prospectively in LS-SCLC patients receiving prophylactic cerebral irradiation (PCI).METHODS: Data in patients treated with PCI from the CONVERT trial was analysed.RESULTS: 449/547 (82%) received PCI after completion of chemoradiotherapy. Baseline brain imaging consisted of CT-scan in 356/449 patients (79%) and MRI in 83/449 (18%) patients. PCI was delivered to 220/273 participants (81%) in the twice-daily (BD) group and 229/270 in the once-daily (OD) group (85%; p=0.49). Total median PCI dose was 25Gy in both BD and OD groups (p=0.74). In patients who received PCI, 75 (17%) developed BM (35 [8%] in OD and 40 [9%] in BD) and 173 (39%) other extracranial progression. In the univariate analysis, GTV was associated with an increased risk of BM (p=0.007) or other radiological progression events (p=0.006), whereas in a multivariate analysis both thoracic GTV (tGTV) and PS were associated with either progression type. The median OS of patients treated with PCI was 29 months. In the univariate analysis of OS, PCI timing from end of chemotherapy, weight loss >10%, and tGTV were prognostic factors associated with OS. In the multivariate analysis, only tGTV was associated with OS. Delay between end of chemotherapy and PCI was not associated with OS.CONCLUSION: Patients receiving OD or BD thoracic RT have the same risk of developing BM. Larger tumours are associated with a higher risk of BM.
KW - Cranial irradiation
KW - Lung cancer
KW - Phase III trial
UR - http://www.scopus.com/inward/record.url?scp=85056645832&partnerID=8YFLogxK
U2 - 10.1016/j.jtho.2018.09.019
DO - 10.1016/j.jtho.2018.09.019
M3 - Article
C2 - 30292850
SN - 1556-0864
VL - 14
SP - 294
EP - 297
JO - Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
JF - Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
IS - 2
ER -