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Immediate Side Effects of Cranial Stereotactic Radiosurgery and ...

Immediate Side Effects of Cranial Stereotactic Radiosurgery and ...

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Mohamad Abdulla 331receive a radiation dose ranging from 0-8.1 Gywith a median value <strong>of</strong> 1.21 Gy to the regionlocated at the floor <strong>of</strong> the 4th ventricle <strong>and</strong>harboring area postrema, but the onset <strong>of</strong> vomitingwas correlated only with doses greater than2 Gy, contrasting to data reported by Alex<strong>and</strong>eret al. [1].The discrepancy with data reported by Alex<strong>and</strong>er<strong>and</strong> co-workers [1] could be attributed todifferent disease entities treated in our study,where he treated only cases with acuostic neuromas.However, further analysis <strong>of</strong> our datarevealed that 33% (7/21 patients) with acuosticneuromas had developed nausea <strong>and</strong> vomitingbut at a lower threshold dose level (2 versus6.18 Gy) to area postrema, a finding whichrequires further clarification via future studiesenrolling higher number <strong>of</strong> patients to establishthe threshold radiation dose to area postremaabove which, nausea <strong>and</strong> vomiting are anticipatedas immediate post-stereotxay morbid events.Also, inspite <strong>of</strong> the relatively close results withthose <strong>of</strong> Bodis et al. [4]; (2 versus 2.75 Gy) asa threshold dose level to area postrema, none <strong>of</strong>our patients had received ondansetron as a premedication;only metclopramide <strong>and</strong> steroidswhich were effecive in alleviating such manifestations.The incidence <strong>of</strong> developing immediate sideeffects among patients with malignant craniallesions was clearly higher than those with benigndiseases, 70% versus 43% indicating the needto pay more attention to proper patient selection<strong>and</strong> adequate pre- as well a post-treatment medicationsfor patients with high grade gliomas<strong>and</strong> brain metastases.Only two patients had developed epilepticepisodes following stereotaxy. They had thediagnoses <strong>of</strong> high grade glioma <strong>and</strong> brainmetastasis, also they had a past history <strong>of</strong> convulsivefits during their disease course <strong>and</strong> coulddirect attention to the importance <strong>of</strong> employingmore potent anti-convulsive measures whenattempting to treat similar patients.Worsening <strong>of</strong> pre-therapy manifestations wasreported in one, two <strong>and</strong> two patients with diagnoses<strong>of</strong> low grade glioma, high garde glioma<strong>and</strong> meningioma respectively. All lesions werenoted to be located near the motor cortex whichcould be compromised by either direct radiationeffect or more likely due to cerebral oedemam<strong>and</strong>ating the adequate use <strong>of</strong> dehydrating measuresin both pre- <strong>and</strong> post-therapy periods.Moreover, It is difficult to conclude that patientswith pituitary adenomas are not anticipated todevelop immediate post-stereotaxy side effects,as this conclusion cannot be emphasized withthe small number <strong>of</strong> patients enrolled in our trial(8 Patients).The location <strong>of</strong> lesions <strong>and</strong> dose are criticalparameters related to the development <strong>of</strong> poststereotacticradiosurgery <strong>and</strong> radiotherapy edema.It is well known that parasagittal meningiomasare a risk group in this respect. Occlusion <strong>of</strong>bridging veins is a possible though unprovenmechanism for this phenomenon. However, thisedema did not occur within the time frame <strong>of</strong>the present study.Further clinical trials are clearly neededincluding higher numbers <strong>of</strong> patients with homogenouscharacteristics aiming at obtainingmore informative data about stereotaxy sideeffects <strong>and</strong> its proper management. Also, it shouldbe emphasized to avoid radiation doses greaterthan 2 Gy to the region in the floor <strong>of</strong> the 4thventricle harboring area potrema with the possibleuse <strong>of</strong> H3 antagonists if higher dose deliveryis an inevitable event.Acknowledgment: I am grateful to Pr<strong>of</strong>. KamalA. El-Ghamrawi for critical review <strong>of</strong> Themainscript. Also, I would like to express mydeep appreciation to Pr<strong>of</strong>. Ehsan El-Ghoneimy& Pr<strong>of</strong>. Magda Moustafa as well as NEMROCKradiosurgery team for devotion <strong>and</strong> help.REFERENCES1- Alex<strong>and</strong>er E. 3rd, Siddon R <strong>and</strong> Loeffler J.: The AcuteOnset <strong>of</strong> Nausea <strong>and</strong> Vomiting Following <strong>Stereotactic</strong><strong>Radiosurgery</strong>: Correlation with Total Dose to AreaPostrema. Surg. Neurol., 32 (1): 40-44, 1989.2- Alex<strong>and</strong>er E. III, Loeffler J.S., Lunsford L.D., et al.:<strong>Stereotactic</strong> <strong>Radiosurgery</strong>. New York: McGraw Hill,1993.3- Altman D.G.: Practical statistics for medical research.London, Chapman & Hall, 115-231, 1991.4- Bodis S., Alex<strong>and</strong>er E. III, Kooy H., et al.: The Prevention<strong>of</strong> <strong>Radiosurgery</strong>-Induced Nausea <strong>and</strong> Vomitingby Ondansetron: Evidence <strong>of</strong> a Direct Effect on TheCentral Nervous System Chemoreceptor Trigger Zone.Surg. Neurol., 42: 249-252, 1994.5- Brenner D.J., Martel M.K. <strong>and</strong> Hall E.J.: FractionatedRegimens For <strong>Stereotactic</strong> Radiotherapy <strong>of</strong> RecurrentTumors in The Brain. Int. J. Radiat. Oncol. Biol. Phys.,21: 819-824, 1991.

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