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   <subfield code="a">10.1007/s11547-012-0909-4</subfield>
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   <subfield code="a">Neoadjuvant oxaliplatin and 5-fluorouracil with concurrent radiotherapy in patients with locally advanced rectal cancer: a singleinstitution experience</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[D. Greto, F. Paiar, C. Saieva, A. Galardi, M. Mangoni, L. Livi, B. Agresti, D. Franceschini, P. Bonomo, V. Scotti, B. Detti, F. Tonelli, A. Valeri, L. Messerini, G. Biti]</subfield>
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   <subfield code="a">Radioterapia neoadiuvante associata ad oxaliplatino e 5-fluorouracile in pazienti affetti da tumore rettale localmente avanzato: l'esperienza di un singolo centro</subfield>
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   <subfield code="a">Purpose: The aim of this study was to evaluate the rate of pathological response (PR), disease control and safety of neoadjuvant chemotherapy using oxaliplatin (OX) and 5-fluorouracil (5-FU) with concurrent radiotherapy for treating locally advanced rectal cancer. Materials and methods: Between November 2002 and December 2010, 90 patients with locally advanced rectal cancer treated with neoadjuvant chemoradiotherapy (CRT) were retrospectively analysed. All patients underwent preoperative radiotherapy (45 Gy in 1.8-Gy fractions) with concurrent OX (80 mg/m2 i.v., day 1) and a 120-h continuous infusion of 5-FU (1,000 mg/m2 per day). Surgery was performed within 6 weeks after completion of CRT treatment. Results: Complete pathological response was obtained in six patients (6.7%), and 39 (43.3%) had their disease downstaged. The median follow-up period was 4.7 years (6 months to 9 years). Local recurrence occurred in two patients (2.2%), one of whom developed also liver metastases. Distant metastases not associated with local relapse occurred in 23 (25.6%) patients. Overall (OS) and disease-free (DFS) survival were 62.9% and 52.8%, respectively. CRT was well tolerated, with only one grade 3 (1.2%) haematological toxicity (neutropaenia). Conclusions: Neoadjuvant systemic chemotherapy based on OX and 5-UC associated with radiotherapy is well tolerated, with good results in terms of pathological response, disease control and survival, in rectal cancer patients.</subfield>
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   <subfield code="a">Springer-Verlag Italia, 2013</subfield>
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   <subfield code="a">Locally advanced rectal cancer</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Chemoradiotherapy</subfield>
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   <subfield code="a">Oxaliplatin</subfield>
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   <subfield code="a">Tumore del retto localmente avanzato</subfield>
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   <subfield code="a">Radio-chemioterapia</subfield>
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   <subfield code="a">Oxaliplatino</subfield>
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   <subfield code="a">Greto</subfield>
   <subfield code="D">D.</subfield>
   <subfield code="u">Radiotherapy Unit, University of Florence, Viale Morgagni 85, 50134, Florence, Italy</subfield>
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   <subfield code="a">Paiar</subfield>
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   <subfield code="u">Radiotherapy Unit, University of Florence, Viale Morgagni 85, 50134, Florence, Italy</subfield>
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   <subfield code="a">Saieva</subfield>
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   <subfield code="u">Molecular and Nutritional Epidemiology Unit, Cancer Research and Prevention Center, Scientific Institute of Tuscany, Florence, Italy</subfield>
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   <subfield code="a">Galardi</subfield>
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   <subfield code="a">Mangoni</subfield>
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   <subfield code="a">Livi</subfield>
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   <subfield code="u">Radiotherapy Unit, IFCA, University of Florence, Florence, Italy</subfield>
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   <subfield code="a">Agresti</subfield>
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   <subfield code="a">Franceschini</subfield>
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   <subfield code="a">Bonomo</subfield>
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   <subfield code="a">Tonelli</subfield>
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   <subfield code="t">La radiologia medica</subfield>
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