2008
DOI: 10.1080/02656730701881125
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Incidence of acute peripheral neurotoxicity after deep regional hyperthermia of the pelvis

Abstract: Acute neurotoxicity following hyperthermia for pelvic tumours is a rare complication, but can result in symptoms affecting the activities of daily life. We found no patient, tumour or treatment characteristics predictive for a risk of neurotoxicity.

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Cited by 6 publications
(6 citation statements)
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“…4,5 Despite the complementary nature of hyperthermia- and IR-induced cell killing, the precise mechanism of heat-induced cell death is not yet clear, and the synergistic interaction between heat and IR in cell killing is even less well understood. Because phase III clinical trials have shown significant benefits from adding hyperthermia to radiotherapy regimens for a number of malignancies, 6,7 understanding the mechanisms involved in heat-mediated IR sensitization has become clinically important. This review will focus on the possible role of hyperthermia in DNA damage response and transcriptional regulation of heat shock proteins in the context of enhancing the potential of targeted radiotherapy.…”
Section: Introductionmentioning
confidence: 99%
“…4,5 Despite the complementary nature of hyperthermia- and IR-induced cell killing, the precise mechanism of heat-induced cell death is not yet clear, and the synergistic interaction between heat and IR in cell killing is even less well understood. Because phase III clinical trials have shown significant benefits from adding hyperthermia to radiotherapy regimens for a number of malignancies, 6,7 understanding the mechanisms involved in heat-mediated IR sensitization has become clinically important. This review will focus on the possible role of hyperthermia in DNA damage response and transcriptional regulation of heat shock proteins in the context of enhancing the potential of targeted radiotherapy.…”
Section: Introductionmentioning
confidence: 99%
“…The development of neurotoxicity was more frequent in the mEHT Group however cisplatin was a perfect predictor of neurotoxicity in the multivariate regression analysis and was therefore the most likely cause of the development of neurotoxicity. Although peripheral neuropathy is a known but rare side effect of HT to the pelvis [5,17] and we therefore cannot exclude the potential effects of deep heating on the development of peripheral neuropathy related to increased local effectiveness.…”
Section: Discussionmentioning
confidence: 99%
“…A retrospective analysis of 420 patients treated with RT and HT reported that 153(36%) participants developed subcutaneous tissue toxicity, ranging from grade 1-3 in severity, with one patient requiring surgical intervention [16]. Acute neurotoxicity following the treatment of deep pelvic tumors with HT is a rare (2.3% incidence) complication which can have an impact on the daily activities of the patient [5,17].…”
Section: Introductionmentioning
confidence: 99%
“…Toxicity from whole-body-HT depends on the patient's general and the physiological conditions during the treatment [81]. Serious toxicity from regional HT perfusion with modern technology and proper choice of perfusate composition, flow rate and pressure, blood gas values, drug doses, temperature dose and scheduling, is limited [118,119].…”
Section: Hyperthermia-induced Toxicitymentioning
confidence: 99%