Source:http://linkedlifedata.com/resource/pubmed/id/16110138
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007137,
umls-concept:C0008838,
umls-concept:C0016360,
umls-concept:C0023413,
umls-concept:C0144576,
umls-concept:C0205179,
umls-concept:C0282460,
umls-concept:C0332283,
umls-concept:C0444889,
umls-concept:C0460004,
umls-concept:C0521115,
umls-concept:C0679729,
umls-concept:C1517927,
umls-concept:C1518578
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pubmed:issue |
3
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pubmed:dateCreated |
2005-8-19
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pubmed:abstractText |
The primary objective of this phase II study was to access the complete response (CR) rate to a new innovative induction regimen in patients with locally advanced head and neck cancer (LA-HNC). From October 2000 until October 2003 a total of 38 eligible patients (33 men and 5 women) entered the study. The large majority of them presented with a performance status of 0-1 and with clinical stage IV disease. Treatment consisted of three cycles of induction chemotherapy (IC) with paclitaxel 175 mg/m2 in a 3-h infusion on d 1, leucovorin (LV) 200 mg/m2 over 20 min immediately followed by FU 400 mg/m2 bolus and then 600 mg/m2 as a 24-h continuous infusion on d 1 and 2 and a cisplatin 75 mg/m2 over 1-h infusion on d 2 every 3 wk. This was then followed by radiation (70 Gy) and weekly cisplatin 40 mg/m2. After the completion of IC, 6/38 (16%) patients had CR. The CR rate was increased to 66% post-concomitant chemoradiotherapy (CCRT). Neutropenia (37.5%), pain (62%), nausea/vomiting (21%), and alopecia (79%) were the most frequent side effects during IC. The most pronounced toxicities during chemoradiotherapy were stomatitis (62.5%) and xerostomia (53%). Median time to progression was 11.0 mo and median survival 16.7 mo. One- and 2-yr survival rates were 73% and 38%, respectively. In conclusion, this novel induction regimen is active, is well tolerated, and can be successfully followed by CCRT with weekly cisplatin. CCRT should remain standard treatment for patients with LA-HNC. Novel induction combinations, such as that reported in the present study, should be evaluated in combination with CCRT only in the context of clinical trials.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
1357-0560
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pubmed:author |
pubmed-author:AthanassiouEleniE,
pubmed-author:BamiasAristotelisA,
pubmed-author:DaniilidisJohnJ,
pubmed-author:EconomopoulosTheofanisT,
pubmed-author:FountzilasGeorgeG,
pubmed-author:Kalogera-FountzilaAnnaA,
pubmed-author:KaranastassiSophiaS,
pubmed-author:KarinaMariaM,
pubmed-author:MakatsorisThomasT,
pubmed-author:MisailidouDespinaD,
pubmed-author:NikolaouAngelosA,
pubmed-author:PavlidisNicholasN,
pubmed-author:SamantasEpaminondasE,
pubmed-author:SkarlosDimosthenisD,
pubmed-author:TolisChristosC,
pubmed-author:TsekerisPeriklisP,
pubmed-author:ZamboglouNikolasN
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pubmed:issnType |
Print
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
269-79
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16110138-Adult,
pubmed-meshheading:16110138-Aged,
pubmed-meshheading:16110138-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:16110138-Carcinoma, Squamous Cell,
pubmed-meshheading:16110138-Cisplatin,
pubmed-meshheading:16110138-Combined Modality Therapy,
pubmed-meshheading:16110138-Female,
pubmed-meshheading:16110138-Fluorouracil,
pubmed-meshheading:16110138-Head and Neck Neoplasms,
pubmed-meshheading:16110138-Humans,
pubmed-meshheading:16110138-Infusions, Intravenous,
pubmed-meshheading:16110138-Injections, Intravenous,
pubmed-meshheading:16110138-Leucovorin,
pubmed-meshheading:16110138-Male,
pubmed-meshheading:16110138-Middle Aged,
pubmed-meshheading:16110138-Paclitaxel,
pubmed-meshheading:16110138-Treatment Outcome
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pubmed:year |
2005
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pubmed:articleTitle |
Paclitaxel, cisplatin, leucovorin, and continuous infusion fluorouracil followed by concomitant chemoradiotherapy for locally advanced squamous cell carcinoma of the head and neck: a Hellenic Cooperative Oncology Group Phase II Study.
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pubmed:affiliation |
Department of Medical Oncology, PAPAGEORGIOU General Hospital, Aristotle University of Thessaloniki School of Medicine, Thessaloniki, Greece. fountzil@med.auth.gr
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Multicenter Study,
Clinical Trial, Phase II
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