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Guidelines for Complications of Cancer Treatment Vol VIII Part B

Guidelines for Complications of Cancer Treatment Vol VIII Part B

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RT to brain has been implicated as one <strong>of</strong> the mostimportant factor associated with neuroendocrinedysfunction after long term follow up.Radiation dose and volume <strong>of</strong> brain irradiated had shownsignificant correlation. Majority <strong>of</strong> the literature hascome from either craniospinal radiation (CSI) or fromwhole brain RT.Both in whole brain RT and CSI, PHA receives highdose and thus functional impairment is expected evenyears after RT. Growth hormone (GH) seems to be themost sensitive hormone as it’s serum level is the first todecline after RT. GH is followed by thyroid hormonereleasing hormone (THRH) and cortisol level decline.Impairment <strong>of</strong> the circadian hormonal surge is consideredas an early sign <strong>of</strong> hormone axis deficit.Frequency, delay <strong>of</strong> appearance and severity <strong>of</strong>deficiency depends upon RT dose delivered, age <strong>of</strong> thepatient and treatment schedule.After conventional whole brain RT (WBRT) with dosemore than 18 Gy, impairment <strong>of</strong> normal growth hormone(GH) secretion are the first and most common recognizeddeficit.After CSI, 50% to 80% <strong>of</strong> patients develop signs <strong>of</strong> GHdeficiency, 30-50% develops primary hypothyroidismand 30-40% develops cortisol deficiency.Functional disturbances <strong>of</strong> thyroid and adrenal glandsdue to PH axis deficiency are less common and usuallyseen only after RT dose >40 Gy.Few chemotherapeutic regimens used in brain tumor arealso associated with decline in endocrine function.Patients with hormonal dysfunction presents with earlyor delayed puberty or growth retardation. Girls mayfrequently experience an early and rapid pubertal350

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