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Hemorrhagic complications in a phase II study of sunitinib in patients of nasopharyngeal carcinoma who has previously received high-dose radiation.

Authors :
Hui, E. P.
Ma, B. B. Y.
King, A. D.
Mo, F.
Chan, S. L.
Kam, M. K. M.
Loong, H. H.
Ahuja, A. T.
Zee, B. C. Y.
Chan, A. T. C.
Source :
Annals of Oncology. Jun2011, Vol. 22 Issue 6, p1280-1287. 8p. 2 Black and White Photographs, 3 Charts.
Publication Year :
2011

Abstract

Background: We aimed to evaluate the safety and efficacy of single-agent sunitinib in nasopharyngeal carcinoma (NPC).Methods: Eligible patients had progressive disease after prior platinum-based chemotherapy. Sunitinib was given as continuous once-daily dosing of 37.5 mg in 4-week cycles until progression.Results: Thirteen patients were enrolled. Recruitment was stopped after two patients died of hemorrhagic events. All patients had previously received curative radiotherapy (RT) to nasopharynx/neck (including nine patients who had chemoradiotherapy). Patients received a median of three cycles of sunitinib. One patient was still on sunitinib with stable disease after 24 cycles. Hemorrhagic events occurred in nine patients (64%), including epistaxis in six, hemoptyses in three and hematemesis in two patients. Prior RT to thorax was significantly associated with hemoptyses (P = 0.03). Two patients with local tumor invasion into the carotid sheath developed fatal epistaxis/hematemesis within the first cycle of sunitinib, likely due to internal carotid blowout after tumor shrinkage.Conclusions: Sunitinib demonstrated modest clinical activity in heavily pretreated NPC patients. However, the high incidence of hemorrhage from the upper aerodigestive tract in NPC patients who received prior high-dose RT to the region is of concern. Direct vascular invasion by tumors appeared to increase the risk of serious bleeding. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09237534
Volume :
22
Issue :
6
Database :
Academic Search Index
Journal :
Annals of Oncology
Publication Type :
Academic Journal
Accession number :
61048777
Full Text :
https://doi.org/10.1093/annonc/mdq629