dc.contributor.author |
Kouloulias, V |
en |
dc.contributor.author |
Plataniotis, G |
en |
dc.contributor.author |
Kouvaris, J |
en |
dc.contributor.author |
Dardoufas, C |
en |
dc.contributor.author |
Gennatas, C |
en |
dc.contributor.author |
Uzunoglu, N |
en |
dc.contributor.author |
Papavasiliou, C |
en |
dc.contributor.author |
Vlahos, L |
en |
dc.date.accessioned |
2014-03-01T01:21:59Z |
|
dc.date.available |
2014-03-01T01:21:59Z |
|
dc.date.issued |
2005 |
en |
dc.identifier.issn |
0277-3732 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/16424 |
|
dc.subject |
5-fluoroucil and mitomycin |
en |
dc.subject |
Anal cancer |
en |
dc.subject |
Intracavitary hyperthermia |
en |
dc.subject |
Radiotherapy |
en |
dc.subject |
Randomized study |
en |
dc.subject.classification |
Oncology |
en |
dc.subject.other |
fluorouracil |
en |
dc.subject.other |
mitomycin C |
en |
dc.subject.other |
adult |
en |
dc.subject.other |
aged |
en |
dc.subject.other |
anus |
en |
dc.subject.other |
anus cancer |
en |
dc.subject.other |
anus sphincter |
en |
dc.subject.other |
article |
en |
dc.subject.other |
bladder disease |
en |
dc.subject.other |
blood toxicity |
en |
dc.subject.other |
clinical trial |
en |
dc.subject.other |
colostomy |
en |
dc.subject.other |
controlled clinical trial |
en |
dc.subject.other |
controlled study |
en |
dc.subject.other |
enteropathy |
en |
dc.subject.other |
female |
en |
dc.subject.other |
human |
en |
dc.subject.other |
hyperthermic therapy |
en |
dc.subject.other |
male |
en |
dc.subject.other |
microwave irradiation |
en |
dc.subject.other |
morbidity |
en |
dc.subject.other |
radiation dose |
en |
dc.subject.other |
randomized controlled trial |
en |
dc.subject.other |
rectum |
en |
dc.subject.other |
recurrent disease |
en |
dc.subject.other |
skin toxicity |
en |
dc.subject.other |
survival |
en |
dc.subject.other |
Aged |
en |
dc.subject.other |
Antineoplastic Combined Chemotherapy Protocols |
en |
dc.subject.other |
Anus Neoplasms |
en |
dc.subject.other |
Combined Modality Therapy |
en |
dc.subject.other |
Diathermy |
en |
dc.subject.other |
Dose Fractionation |
en |
dc.subject.other |
Female |
en |
dc.subject.other |
Fluorouracil |
en |
dc.subject.other |
Humans |
en |
dc.subject.other |
Male |
en |
dc.subject.other |
Middle Aged |
en |
dc.subject.other |
Mitomycin |
en |
dc.subject.other |
Survival Analysis |
en |
dc.title |
Chemoradiotherapy combined with intracavitary hyperthermia for anal cancer: Feasibility and long-term results from a phase II randomized trial |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1097/01.coc.0000139939.60056.42 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1097/01.coc.0000139939.60056.42 |
en |
heal.language |
English |
en |
heal.publicationDate |
2005 |
en |
heal.abstract |
Purpose: The purpose of this study was to investigate in a randomized way the clinical benefit of addition of intracavitary hyperthermia (ICHT) to a conventional chemoradiotherapy schedule in patients with T2-T3N0M0 anal cancer. Methods and Materials: Patients were randomly assigned to undergo chemotherapy with 5-fluorouracil (5-FU) and mitomycin-C combined with radiotherapy with (arm A: 24 patients) or without ICHT (arm 13: 25 patients). A microwave applicator operating at 43 3 MHz inserted into the anal-rectal cavity was used for ICHT. Patients in both aims received 1000 mg/m(2) per day of 5-FU on days 1-4 and days 28-31 plus 15 mg/m(2) mitomycin-C on day 1. Radiotherapy was administered with a dose of 41.4 Gy (1.8 Gy per fraction) plus a booster dose of 14 Gy (2 Gy per fraction). Results: One patient from group A developed severe mucositis, whereas no severe morbidity was noted in the rest of the patients in both groups. The incidence of lower-intestine acute reactions was higher in the ICHT arm. After a 5-year follow up in the hyperthermia arm, 23 of 24 patients (95.8%) preserved their anorectal function and avoided permanent colostomy, whereas in the second arm, 17 of 25 (68.0%) had sphincter preservation. Local recurrence-free survival time was significantly higher in the ICHT arm (P = 0.0107, log rank test), whereas no significant difference in overall survival was note I. Conclusion: The addition of ICHT to the chemoradiotherapy schedule of anal cancer seems to offer a new effective and safe therapeutic modality. The preservation of anorectal function seems to be the significant clinical benefit of adjuvant ICHT. |
en |
heal.publisher |
LIPPINCOTT WILLIAMS & WILKINS |
en |
heal.journalName |
American Journal of Clinical Oncology: Cancer Clinical Trials |
en |
dc.identifier.doi |
10.1097/01.coc.0000139939.60056.42 |
en |
dc.identifier.isi |
ISI:000226851500016 |
en |
dc.identifier.volume |
28 |
en |
dc.identifier.issue |
1 |
en |
dc.identifier.spage |
91 |
en |
dc.identifier.epage |
99 |
en |