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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
3                            CHART (continuous hyperfractionated accelerated radiotherapy) is the most
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
6 nce-daily RT cohorts) or 1.5 Gy twice a day (hyperfractionated cohorts).
7 eived induction chemotherapy, dose-escalated hyperfractionated craniospinal radiotherapy, and mainten
8  to conventionally fractionated CRT (CFX) or hyperfractionated CRT (HFX) to a total dose of 18 Gy.
9             BP patients received hyper-CVAD (hyperfractionated cyclophosphamide, vincristine, adriamy
10 ients with Ph(+) ALL who received first-line hyperfractionated cyclophosphamide, vincristine, doxorub
11            Patients received eight cycles of hyperfractionated cyclophosphamide, vincristine, doxorub
12 st reported results have been with rituximab-hyperfractionated cyclophosphamide-vincristine-doxorubic
13 ard) or twice daily for 2 consecutive weeks (hyperfractionated) during a 21-day cycle.
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
17  is more efficacious and not more toxic than hyperfractionated irradiation alone.
18 otherapy (combined treatment) is superior to hyperfractionated irradiation alone.
19                      We investigated whether hyperfractionated irradiation plus concurrent chemothera
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
24 sophagitis >/= grade 3 in patients receiving hyperfractionated radiation and chemotherapy.
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
27 fluorouracil administration and accelerated, hyperfractionated radiation therapy.
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
31                       The comparison between hyperfractionated radiotherapy and concomitant chemoradi
32                                 Split-course hyperfractionated radiotherapy did not increase the rate
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
36                                           In hyperfractionated radiotherapy the dose per fraction is
37 livered in daily 2-Gy fractions to 70 Gy, or hyperfractionated radiotherapy was delivered in 1.25-Gy
38 mide, and vincristine, and a split course of hyperfractionated radiotherapy.
39 a significant OS benefit from accelerated or hyperfractionated radiotherapy; a similar but nonsignifi
40           Forty patients (30 standard and 10 hyperfractionated) received 533 injections of ONYX-015.
41 ain (47% on the standard regimen, 80% on the hyperfractionated regimen).
42 Gy/d), and the final three patients received hyperfractionated RT (76.8 Gy, 1.2 Gy bid).
43 zed to receive conventional RT (C-RT) versus hyperfractionated RT (HF-RT).
44         A greater difference was evident for hyperfractionated RT and platinum-based chemotherapy.
45            Concurrent chemoradiotherapy with hyperfractionated RT is feasible in this patient populat
46             Subset analysis of studies using hyperfractionated RT revealed OS RR for ERT versus LRT o
47 we added paclitaxel to the FHX base and used hyperfractionated RT to determine the maximum-tolerated
48    The addition of infusional paclitaxel and hyperfractionated RT to FHX is feasible.
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
51           Radiation consisted of accelerated hyperfractionated thoracic radiation (AHTRT) 1.5 Gy bid
52 e (PIEo) given concurrently with accelerated hyperfractionated thoracic radiation was studied in pati
53       The cytoreductive regimen consisted of hyperfractionated total body irradiation (HFTBI), thiote
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
57                                              Hyperfractionated treatment resulted in 10% complete res
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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