Feasibility and safety of dose-dense modified docetaxel-cisplatin or carboplatin and 5-fluorouracil regimen (mTPF) in locally advanced or metastatic head and neck cancers: a retrospective monocentric study

Verfasser / Beitragende:
[Séna Yossi, Benjamin Linot, Guillaume Peyraga, Renaud Breheret, Laurent Laccourreye, Olivier Capitain]
Ort, Verlag, Jahr:
2015
Enthalten in:
International Journal of Clinical Oncology, 20/6(2015-12-01), 1086-1092
Format:
Artikel (online)
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024 7 0 |a 10.1007/s10147-015-0836-1  |2 doi 
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245 0 0 |a Feasibility and safety of dose-dense modified docetaxel-cisplatin or carboplatin and 5-fluorouracil regimen (mTPF) in locally advanced or metastatic head and neck cancers: a retrospective monocentric study  |h [Elektronische Daten]  |c [Séna Yossi, Benjamin Linot, Guillaume Peyraga, Renaud Breheret, Laurent Laccourreye, Olivier Capitain] 
520 3 |a Abstract : Background: Docetaxel-cisplatin and 5-fluorouracil (TPF) chemotherapy (days 1-21) represents a standard but toxic regimen for advanced head and neck cancer (HNC). We report a retrospective monocentric study evaluating the safety and the efficacy of a dose-dense modified TPF (mTPF) regimen (days 1-14) in patients with stage III-IV HNC. Methods: Thirty-seven patients retrospectively included from May 2011 to May 2014 were treated with a bimonthly dose-dense mTPF regimen (40mg/m2 docetaxel, 40mg/m2 cisplatin or AUC2 carboplatin, folinic acid 400mg/m2 for 2h, bolus 5-FU 400mg/m2 for 10min and 5-FU 1,000mg/m2/day) by continuous infusion over 46h). Results: Chemotherapy was used as induction or palliative treatment in 12 and 25 patients, respectively, with a median age of 60 years (range 46−83). Median follow-up time was 7.4months (2.53-16.7months). There was no intestinal toxicity in 25 patients (68%). Grade 3-4 hematological toxicity was noticed for 5 (13.5%) patients. Granulocyte-colony stimulating factor was used as primary prophylaxis in 30 patients (81%). After at least 4 delivered cycles, complete responses, partial responses and stable diseases were reported in 5 (15%), 13 (39%) and 5 (15%) of the 33 evaluable patients, respectively, yielding an objective response rate of 54.5% (39% for palliative chemotherapy and 90% for induction chemotherapy). Conclusion: Dose-dense mTPF (days 1-14) is safe and seems to be as effective as TPF (days 1-21). Future prospective trials are required to confirm our results. 
540 |a Japan Society of Clinical Oncology, 2015 
690 7 |a 5-fluorouracil  |2 nationallicence 
690 7 |a Docetaxel  |2 nationallicence 
690 7 |a Cisplatin  |2 nationallicence 
690 7 |a Head and neck cancer  |2 nationallicence 
690 7 |a Dose-dense chemotherapy  |2 nationallicence 
690 7 |a Quality of life  |2 nationallicence 
700 1 |a Yossi  |D Séna  |u Department of Oncopharmacology-Pharmacogenetics, Integrated Center of Oncology (ICO) Paul Papin, 2 rue Moll, 49033, Angers Cedex 9, France  |4 aut 
700 1 |a Linot  |D Benjamin  |u Department of Oncopharmacology-Pharmacogenetics, Integrated Center of Oncology (ICO) Paul Papin, 2 rue Moll, 49033, Angers Cedex 9, France  |4 aut 
700 1 |a Peyraga  |D Guillaume  |u Department of Oncopharmacology-Pharmacogenetics, Integrated Center of Oncology (ICO) Paul Papin, 2 rue Moll, 49033, Angers Cedex 9, France  |4 aut 
700 1 |a Breheret  |D Renaud  |u Head and Neck Surgery Department, Centre Hospitalier Universitaire, 4 Rue Larrey, 49100, Angers, France  |4 aut 
700 1 |a Laccourreye  |D Laurent  |u Head and Neck Surgery Department, Centre Hospitalier Universitaire, 4 Rue Larrey, 49100, Angers, France  |4 aut 
700 1 |a Capitain  |D Olivier  |u Department of Oncopharmacology-Pharmacogenetics, Integrated Center of Oncology (ICO) Paul Papin, 2 rue Moll, 49033, Angers Cedex 9, France  |4 aut 
773 0 |t International Journal of Clinical Oncology  |d Springer Japan  |g 20/6(2015-12-01), 1086-1092  |x 1341-9625  |q 20:6<1086  |1 2015  |2 20  |o 10147 
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900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Yossi  |D Séna  |u Department of Oncopharmacology-Pharmacogenetics, Integrated Center of Oncology (ICO) Paul Papin, 2 rue Moll, 49033, Angers Cedex 9, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Linot  |D Benjamin  |u Department of Oncopharmacology-Pharmacogenetics, Integrated Center of Oncology (ICO) Paul Papin, 2 rue Moll, 49033, Angers Cedex 9, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Peyraga  |D Guillaume  |u Department of Oncopharmacology-Pharmacogenetics, Integrated Center of Oncology (ICO) Paul Papin, 2 rue Moll, 49033, Angers Cedex 9, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Breheret  |D Renaud  |u Head and Neck Surgery Department, Centre Hospitalier Universitaire, 4 Rue Larrey, 49100, Angers, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Laccourreye  |D Laurent  |u Head and Neck Surgery Department, Centre Hospitalier Universitaire, 4 Rue Larrey, 49100, Angers, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Capitain  |D Olivier  |u Department of Oncopharmacology-Pharmacogenetics, Integrated Center of Oncology (ICO) Paul Papin, 2 rue Moll, 49033, Angers Cedex 9, France  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t International Journal of Clinical Oncology  |d Springer Japan  |g 20/6(2015-12-01), 1086-1092  |x 1341-9625  |q 20:6<1086  |1 2015  |2 20  |o 10147