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Radioenhancement by cisplatin with accelerated fractionated radiotherapy in a human tumour xenograft
Authors:Joschko  Marion A  Webster  Lorraine K  Bishop  James F  Groves  Janice  Yuen  Kally  Olver  Ian N  Narayan  Kailash N  Ball  David L
Institution:(1) Trescowthick Research Laboratories, Peter MacCallum Cancer Institute, Locked Bag No. 1, A'Beckett Street, Melbourne, VIC 3000, Australia Tel: +61-3-9656-1275 Fax: +61-3-9656-1411 e-mail: lwebster@petermac.unimelb.edu.au, AU;(2) Trescowthick Research Laboratories, Department of Haematology and Medical Oncology, Peter MacCallum Cancer Institute, St. Andrews Place, East Melbourne, VIC 3002, Australia, AU;(3) Department of Medical Oncology, Royal Adelaide Hospital, Adelaide, SA, 5000, Australia, AU;(4) Department of Radiation Oncology, Peter MacCallum Cancer Institute, St. Andrews Place, East Melbourne, VIC 3002, Australia, AU;(5) Statistical Centre, Peter MacCallum Cancer Institute, St. Andrews Place, East Melbourne, VIC 3002, Australia, AU
Abstract:The aim of the present study was to investigate whether cisplatin would enhance the radioresponse of a human tumour xenograft when given in different schedules combined with accelerated fractionated radiation therapy. A human squamous carcinoma of the hypopharynx, FaDu, was grown in the thigh of athymic nude mice. Tumours were exposed to twice-daily 2-Gy fractions, applied 6 h apart over 2 weeks, 5 days a week, alone or combined with cisplatin given at maximally tolerated doses in three different schedules: (1) i.p. as a single bolus (SB) or (2) i.p. as a daily bolus at 30 min before the first daily radiation fraction or (3) s.c. as a continuous infusion through a mini-osmotic pump over 13 days, commencing 24 h prior to the first daily radiation fraction. The end point for the study was tumour growth delay (TGD), calculated as the difference between the delay in regrowth to 200% of the initial tumour size in treated versus control mice. SB cisplatin plus radiation showed only an additive effect on TGD, whereas daily-bolus and continuous-infusion cisplatin demonstrated a greater than additive effect when combined with accelerated fractionated radiation in this human tumour model. Cisplatin appears to be especially beneficial as a radiation enhancer when given throughout the course of radiation. Received: 15 December 1996 / Accepted: 25 March 1997
Keywords:Cisplatin  Radiation enhancement  Tumour growth delay  Xenograft  Squamous carcinoma
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