-
Je něco špatně v tomto záznamu ?
Hyperfractionated accelerated radiotherapy with concomitant integrated boost of 70-75 Gy in 5 weeks for advanced head and neck cancer. A phase I dose escalation study
J. Cvek, J. Kubes, E. Skacelikova, B. Otahal, P. Kominek, M. Halamka, D. Feltl,
Jazyk angličtina Země Německo
Typ dokumentu klinické zkoušky, fáze I, časopisecké články
NLK
ProQuest Central
od 1997-01-01 do 2017-12-31
Medline Complete (EBSCOhost)
od 2006-08-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest)
od 1997-01-01 do 2017-12-31
Health & Medicine (ProQuest)
od 1997-01-01 do 2017-12-31
Public Health Database (ProQuest)
od 1997-01-01 do 2017-12-31
- MeSH
- celková dávka radioterapie MeSH
- dospělí MeSH
- frakcionace dávky záření MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory hlavy a krku patologie radioterapie MeSH
- otorinolaryngologické nádory patologie radioterapie MeSH
- plánování radioterapie pomocí počítače metody MeSH
- přežití bez známek nemoci MeSH
- radiační poranění etiologie MeSH
- radioterapie s modulovanou intenzitou metody MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- spinocelulární karcinom patologie radioterapie MeSH
- staging nádorů MeSH
- tumor burden MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze I MeSH
BACKGROUND AND PURPOSE: The present study was performed to evaluate the feasibility of a new, 5-week regimen of 70-75 Gy hyperfractionated accelerated radiotherapy with concomitant integrated boost (HARTCIB) for locally advanced, inoperable head and neck cancer. METHODS AND MATERIALS: A total of 39 patients with very advanced, stage IV nonmetastatic head and neck squamous cell carcinoma (median gross tumor volume 72 ml) were included in this phase I dose escalation study. A total of 50 fractions intensity-modulated radiotherapy (IMRT) were administered twice daily over 5 weeks. Prescribed total dose/dose per fraction for planning target volume (PTV(tumor)) were 70 Gy in 1.4 Gy fractions, 72.5 Gy in 1.45 Gy fractions, and 75 Gy in 1.5 Gy fractions for 10, 13, and 16 patients, respectively. Uninvolved lymphatic nodes (PTV(uninvolved)) were irradiated with 55 Gy in 1.1 Gy fractions using the concomitant integrated boost. RESULTS: Acute toxicity was evaluated according to the RTOG/EORTC scale; the incidence of grade 3 mucositis was 51% in the oral cavity/pharynx and 0% in skin and the recovery time was ≤ 9 weeks for all patients. Late toxicity was evaluated in patients in complete remission according to the RTOG/EORTC scale. No grade 3/4 late toxicity was observed. The 1-year locoregional progression-free survival was 50% and overall survival was 55%. CONCLUSION: HARTCIB (75 Gy in 5 weeks) is feasible for patients deemed unsuitable for chemoradiation. Acute toxicity was lower than predicted from radiobiological models; duration of dysphagia and confluent mucositis were particularly short. Better conformity of radiotherapy allows the use of more intensive altered fractionation schedules compared with older studies. These results suggest that further dose escalation might be possible when highly conformal techniques (e.g., stereotactic radiotherapy) are used.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13000767
- 003
- CZ-PrNML
- 005
- 20170623110018.0
- 007
- ta
- 008
- 130108s2012 gw f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s00066-012-0128-x $2 doi
- 035 __
- $a (PubMed)22648405
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gw
- 100 1_
- $a Cvek, J $u Department of Oncology, University Hospital Ostrava, 17. listopadu 1790, 70852, Ostrava, Czech Republic. jakub.cvek@fno.cz
- 245 10
- $a Hyperfractionated accelerated radiotherapy with concomitant integrated boost of 70-75 Gy in 5 weeks for advanced head and neck cancer. A phase I dose escalation study / $c J. Cvek, J. Kubes, E. Skacelikova, B. Otahal, P. Kominek, M. Halamka, D. Feltl,
- 520 9_
- $a BACKGROUND AND PURPOSE: The present study was performed to evaluate the feasibility of a new, 5-week regimen of 70-75 Gy hyperfractionated accelerated radiotherapy with concomitant integrated boost (HARTCIB) for locally advanced, inoperable head and neck cancer. METHODS AND MATERIALS: A total of 39 patients with very advanced, stage IV nonmetastatic head and neck squamous cell carcinoma (median gross tumor volume 72 ml) were included in this phase I dose escalation study. A total of 50 fractions intensity-modulated radiotherapy (IMRT) were administered twice daily over 5 weeks. Prescribed total dose/dose per fraction for planning target volume (PTV(tumor)) were 70 Gy in 1.4 Gy fractions, 72.5 Gy in 1.45 Gy fractions, and 75 Gy in 1.5 Gy fractions for 10, 13, and 16 patients, respectively. Uninvolved lymphatic nodes (PTV(uninvolved)) were irradiated with 55 Gy in 1.1 Gy fractions using the concomitant integrated boost. RESULTS: Acute toxicity was evaluated according to the RTOG/EORTC scale; the incidence of grade 3 mucositis was 51% in the oral cavity/pharynx and 0% in skin and the recovery time was ≤ 9 weeks for all patients. Late toxicity was evaluated in patients in complete remission according to the RTOG/EORTC scale. No grade 3/4 late toxicity was observed. The 1-year locoregional progression-free survival was 50% and overall survival was 55%. CONCLUSION: HARTCIB (75 Gy in 5 weeks) is feasible for patients deemed unsuitable for chemoradiation. Acute toxicity was lower than predicted from radiobiological models; duration of dysphagia and confluent mucositis were particularly short. Better conformity of radiotherapy allows the use of more intensive altered fractionation schedules compared with older studies. These results suggest that further dose escalation might be possible when highly conformal techniques (e.g., stereotactic radiotherapy) are used.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a senioři nad 80 let $7 D000369
- 650 _2
- $a spinocelulární karcinom $x patologie $x radioterapie $7 D002294
- 650 _2
- $a přežití bez známek nemoci $7 D018572
- 650 _2
- $a frakcionace dávky záření $7 D019583
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a nádory hlavy a krku $x patologie $x radioterapie $7 D006258
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a staging nádorů $7 D009367
- 650 _2
- $a otorinolaryngologické nádory $x patologie $x radioterapie $7 D010039
- 650 _2
- $a radiační poranění $x etiologie $7 D011832
- 650 _2
- $a celková dávka radioterapie $7 D011879
- 650 _2
- $a plánování radioterapie pomocí počítače $x metody $7 D011880
- 650 _2
- $a radioterapie s modulovanou intenzitou $x metody $7 D050397
- 650 _2
- $a tumor burden $7 D047368
- 655 _2
- $a klinické zkoušky, fáze I $7 D017426
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Kubes, J
- 700 1_
- $a Skacelikova, E
- 700 1_
- $a Otahal, B
- 700 1_
- $a Komínek, Pavel, $d 1958- $7 mzk2003194888
- 700 1_
- $a Halamka, M
- 700 1_
- $a Feltl, D
- 773 0_
- $w MED00010658 $t Strahlentherapie und Onkologie Organ der Deutschen Röntgengesellschaft ... [et al] $x 1439-099X $g Roč. 188, č. 8 (2012), s. 666-70
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/22648405 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20130108 $b ABA008
- 991 __
- $a 20170623110439 $b ABA008
- 999 __
- $a ok $b bmc $g 963549 $s 798931
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2012 $b 188 $c 8 $d 666-70 $i 1439-099X $m Strahlentherapie und Onkologie $n Strahlenther Onkol $x MED00010658
- LZP __
- $a Pubmed-20130108