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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).
- 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.)
- Subjects :
- Carcinoma, Non-Small-Cell Lung diagnostic imaging
Female
France
Humans
Lung Neoplasms diagnostic imaging
Male
Middle Aged
Misonidazole pharmacokinetics
Observer Variation
Radiopharmaceuticals pharmacokinetics
Reproducibility of Results
Sensitivity and Specificity
Survival Rate
Treatment Outcome
Tumor Hypoxia radiation effects
Carcinoma, Non-Small-Cell Lung metabolism
Carcinoma, Non-Small-Cell Lung radiotherapy
Dose Fractionation, Radiation
Lung Neoplasms metabolism
Lung Neoplasms radiotherapy
Misonidazole analogs & derivatives
Subjects
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