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1 py with either total-body irradiation (TBI) (hyperfractionated 15 Gy)/melphalan (180 mg/m(2)) or thio
2 ence between the study treatment (continuous hyperfractionated accelerated radiotherapy [CHART]) and
4 rvations, we developed the CHART (continuous hyperfractionated accelerated radiotherapy) regimen, whi
5 of radiation (RT) in both standard daily and hyperfractionated-accelerated (HA) twice-daily RT schedu
7 eived induction chemotherapy, dose-escalated hyperfractionated craniospinal radiotherapy, and mainten
10 ients with Ph(+) ALL who received first-line hyperfractionated cyclophosphamide, vincristine, doxorub
12 st reported results have been with rituximab-hyperfractionated cyclophosphamide-vincristine-doxorubic
14 platin chemotherapy (100 microg/delivery) or hyperfractionated external beam radiotherapy (EBRT; 15 G
15 of two chemotherapy arms administered before hyperfractionated external-beam radiotherapy (HFEBRT).
16 all survival benefit being restricted to the hyperfractionated group (HR 0.83, 0.74-0.92), with absol
20 d and neck cancer who were treated only with hyperfractionated irradiation received 125 cGy twice dai
21 ped in three types of altered fractionation: hyperfractionated, moderately accelerated, and very acce
22 In lung cancer, randomized trials assessing hyperfractionated or accelerated radiotherapy seem to yi
23 mg/m2 per day, 7 days per week, plus pelvic hyperfractionated radiation 55.2 to 60 Gy at 1.2 Gy bid
25 e and tolerable concomitant chemotherapy and hyperfractionated radiation regimen that induces sustain
26 cell head and neck cancer were treated with hyperfractionated radiation therapy (72 Gy at 1.2 Gy twi
28 ean age = 51.6 yrs) received conventional or hyperfractionated radiotherapy (63-76.8 Gy) for primary
29 aged and randomly assigned to treatment with hyperfractionated radiotherapy (HFRT) or standard (conve
30 mucositis, dysphagia, and xerostomia during hyperfractionated radiotherapy (n = 40) but not standard
33 low-up than the first version of MARCH, that hyperfractionated radiotherapy is, along with concomitan
34 ms to confirm and explain the superiority of hyperfractionated radiotherapy over other altered fracti
35 ompared with conventional radiotherapy, with hyperfractionated radiotherapy showing the greatest bene
37 livered in daily 2-Gy fractions to 70 Gy, or hyperfractionated radiotherapy was delivered in 1.25-Gy
39 a significant OS benefit from accelerated or hyperfractionated radiotherapy; a similar but nonsignifi
47 we added paclitaxel to the FHX base and used hyperfractionated RT to determine the maximum-tolerated
49 s whether shortening treatment duration with hyperfractionated RT would be feasible and improve locor
50 matched allogeneic sibling transplants using hyperfractionated TBI and cyclophosphamide for patients
52 e (PIEo) given concurrently with accelerated hyperfractionated thoracic radiation was studied in pati
54 ied allogeneic HLA-matched sibling BMT after hyperfractionated total body irradiation (TBI) and cyclo
55 tive and graft-versus-host disease regimens (hyperfractionated total body irradiation, cyclophosphami
56 ed myeloablative cytoreduction consisting of hyperfractionated total body irradiation, thiotepa, and
58 a randomized clinical trial to test whether hyperfractionated (twice daily) cranial radiation therap
59 mozolomide (TMZ), and rituximab, followed by hyperfractionated whole-brain radiotherapy (hWBRT) and s
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