Title
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A feasibility study on adaptive F-18-FDG-PET-guided radiotherapy for recurrent and second primary head and neck cancer in the previously irradiated territory
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Author
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Abstract
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To evaluate feasibility, disease control, survival, and toxicity after adaptive F-18-fluorodeoxyglucose (FDG) positron emisson tomography (PET) guided radiotherapy in patients with recurrent and second primary head and neck squamous cell carcinoma. A prospective trial investigated the feasibility of adaptive intensity modulated radiotherapy (IMRT)+/- concomitant cetuximab in 10 patients. The primary endpoint was achieving a 2-year survival free of grade > 3 toxicity in a 30% of patients. Three treatment plans based on 3 PET/CT scans were consecutively delivered in 6 weeks. The range of dose painting was 66.0-85.0Gy in the dose-painted tumoral volumes in 30 fractions. Two-year locoregional and distant control rates were 38 and 76%, respectively. Overall and disease-free survival at 2 years was 20%. No grade 4 or 5 acute toxicity was observed in any of the patients, except for arterial mucosal hemorrhage in 1 patient. Three months after radiotherapy, grade 4 dysphagia and mucosal wound healing problems were observed in 1/7 and 1/6 of patients, respectively. Grade 5 toxicity (fatal bleeding) was seen in 2 patients, at 3.8 and 4.1 months of follow-up. Data on 2aEuroyear toxicity could only be assessed in 1 of the 2 surviving patients, in whom grade 4 mucosal wound healing problems were observed; no other grade > 3 toxicity was observed. In this respect, a 30% 2aEuroyear survival free of grade > 3 toxicity will not be achieved. Adaptive PET-guided reirradiation is feasible. However, due to slow accrual and treatment results that seemed inconsistent with achieving the primary endpoint, the trial was stopped early. |
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Language
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English
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Source (journal)
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Strahlentherapie und Onkologie. - München, 1986, currens
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Publication
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München
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2018
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ISSN
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0179-7158
[print]
1439-099X
[online]
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DOI
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10.1007/S00066-018-1293-3
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Volume/pages
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194
:8
(2018)
, p. 727-736
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ISI
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000439933100004
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Pubmed ID
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29556677
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Full text (Publisher's DOI)
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Full text (publisher's version - intranet only)
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