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   <subfield code="a">10.1007/s12094-012-0911-2</subfield>
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   <subfield code="a">IMRT: preliminary results in a series of advanced head-and-neck cancer patients</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Antonio Vila Capel, Jorge Vilar Palop, Agustín Pedro Olivé, Alberto Sanchez-Reyes Fernandez, Jordi Vayreda Ribera, Joan Julià Sanahuja, Joaquim Pérez de Olaguer Agustín, Nuria Artola Codina, Luis Moya Cascant, Esther Rubio Calatayud, Gemma Carrera Domenech]</subfield>
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   <subfield code="a">Purpose: To determine retrospectively 2-3year local and regional control (LRC), free-of-disease survival (FDS) and overall survival (OS), as well as summarized toxicities in a group of 31 advanced head-and-neck cancer patients, treated at our institution between 2004 and 2011 with definitive IMRT low-dose concomitant boost, the majority of them with concurrent chemotherapy based on cisplatin. The results are also shown in the sub-group of nasopharyngeal cancer patients (NPC: 15 cases). Patients and methods: Radiological basal and contrasted CT series, MR-CT or PET/CT fused images in the setup position with immobilization mask were registered in simulation therapy patients. Planed doses were: 70Gy in primary tumor and positive nodes &gt;1cm; 63Gy in high-risk areas of microscopic diseases +10mm safety margin; and 56Gy in low risk of diseases regional lymph nodes. Treatment was delivered using a Varian 2100 Clinac with sliding windows IMRT. Spinal cord doses were limited to a strict maximum of 45Gy, and optimization aimed for mean doses in parotid glands below 26Gy, especially in the contralateral parotid gland. Online DRR-portal X-ray comparison images were taken every day with a deviation module tolerance ≤3mm. Results: The mean follow-up since IMRT was 34months (interval: 8-89; median 31months). Median follow-up in living patients was 22months. The 2-year rate for global LRC was 64%, for FDS 61% and OS 77%. For the NPC group after 2years, LRC was 73%, FDS 73% and OS 93%. The 3-year rates were similar. Seven patients died as a consequence of local and/or regional progression (mean time 10months). Relapses were observed in eight patients (26%), but only seven could be confirmed by biopsy (22.6%; mean time to relapse: 8.6months). Global acute mucositis was 61% and chronic mucositis was shown in six cases which developed xerostomia (19%) in the first control after IMRT, but 1year later it was reduced to only four patients, two Grade 2 and two Grade 1. Conclusions: No excessive, unwarranted toxicities were observed using concomitant low doses boost in IMRT. High rates of compliance to concurrent chemotherapy were achieved. Late xerostomia associated with this regime decreased 1year after conclusion of treatment. The implementation of IMRT requires advances in imaging for better tumor delineation; otherwise the physician loses the advantage of dose modulation or faces a risk of geographical miss.</subfield>
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   <subfield code="a">Federación de Sociedades Españolas de Oncología (FESEO), 2012</subfield>
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   <subfield code="a">Preliminary results</subfield>
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   <subfield code="a">Vila Capel</subfield>
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   <subfield code="u">Unitat de Radioteràpia i Oncologia, Hospital Plató, C/Plató21, 08006, Barcelona, Spain</subfield>
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   <subfield code="u">Unitat de Radioteràpia i Oncologia, Hospital Plató, C/Plató21, 08006, Barcelona, Spain</subfield>
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   <subfield code="u">Unitat de Radioteràpia i Oncologia, Hospital Plató, C/Plató21, 08006, Barcelona, Spain</subfield>
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