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Phase II Study of a Radiotherapy Total Dose Increase in Hypoxic Lesions Identified by 18 F-Misonidazole PET/CT in Patients with Non-Small Cell Lung Carcinoma (RTEP5 Study).

Authors :
Vera P
Thureau S
Chaumet-Riffaud P
Modzelewski R
Bohn P
Vermandel M
Hapdey S
Pallardy A
Mahé MA
Lacombe M
Boisselier P
Guillemard S
Olivier P
Beckendorf V
Salem N
Charrier N
Chajon E
Devillers A
Aide N
Danhier S
Denis F
Muratet JP
Martin E
Riedinger AB
Kolesnikov-Gauthier H
Dansin E
Massabeau C
Courbon F
Farcy Jacquet MP
Kotzki PO
Houzard C
Mornex F
Vervueren L
Paumier A
Fernandez P
Salaun M
Dubray B
Source :
Journal of nuclear medicine : official publication, Society of Nuclear Medicine [J Nucl Med] 2017 Jul; Vol. 58 (7), pp. 1045-1053. Date of Electronic Publication: 2017 Mar 02.
Publication Year :
2017

Abstract

See an invited perspective on this article on page 1043.This multicenter phase II study investigated a selective radiotherapy dose increase to tumor areas with significant <superscript>18</superscript> F-misonidazole ( <superscript>18</superscript> F-FMISO) uptake in patients with non-small cell lung carcinoma (NSCLC). Methods: Eligible patients had locally advanced NSCLC and no contraindication to concomitant chemoradiotherapy. The <superscript>18</superscript> F-FMISO uptake on PET/CT was assessed by trained experts. If there was no uptake, 66 Gy were delivered. In <superscript>18</superscript> F-FMISO-positive patients, the contours of the hypoxic area were transferred to the radiation oncologist. It was necessary for the radiotherapy dose to be as high as possible while fulfilling dose-limiting constraints for the spinal cord and lungs. The primary endpoint was tumor response (complete response plus partial response) at 3 mo. The secondary endpoints were toxicity, disease-free survival (DFS), and overall survival at 1 y. The target sample size was set to demonstrate a response rate of 40% or more (bilateral α = 0.05, power 1-β = 0.95). Results: Seventy-nine patients were preincluded, 54 were included, and 34 were <superscript>18</superscript> F-FMISO-positive, 24 of whom received escalated doses of up to 86 Gy. The response rate at 3 mo was 31 of 54 (57%; 95% confidence interval [CI], 43%-71%) using RECIST 1.1 (17/34 responders in the <superscript>18</superscript> F-FMISO-positive group). DFS and overall survival at 1 y were 0.86 (95% CI, 0.77-0.96) and 0.63 (95% CI, 0.49-0.74), respectively. DFS was longer in the <superscript>18</superscript> F-FMISO-negative patients ( P = 0.004). The radiotherapy dose was not associated with DFS when adjusting for the <superscript>18</superscript> F-FMISO status. One toxic death (66 Gy) and 1 case of grade 4 pneumonitis (>66 Gy) were reported. Conclusion: Our approach results in a response rate of 40% or more, with acceptable toxicity. <superscript>18</superscript> F-FMISO uptake in NSCLC patients is strongly associated with poor prognosis features that could not be reversed by radiotherapy doses up to 86 Gy.<br /> (© 2017 by the Society of Nuclear Medicine and Molecular Imaging.)

Details

Language :
English
ISSN :
1535-5667
Volume :
58
Issue :
7
Database :
MEDLINE
Journal :
Journal of nuclear medicine : official publication, Society of Nuclear Medicine
Publication Type :
Academic Journal
Accession number :
28254869
Full Text :
https://doi.org/10.2967/jnumed.116.188367