SUCCESSFUL THERAPY FOR TRILATERAL RETINOBLASTOMA

被引:30
作者
NELSON, SC
FRIEDMAN, HS
OAKES, WJ
HALPERIN, EC
TIEN, R
FULLER, GN
HOCKENBERGER, B
SCROGGS, MW
MONCINO, M
KURTZBERG, J
BUCKLEY, EG
机构
[1] DUKE UNIV, MED CTR, DEPT OPHTHALMOL, DURHAM, NC 27710 USA
[2] DUKE UNIV, MED CTR, DEPT PEDIAT, DURHAM, NC 27710 USA
[3] DUKE UNIV, MED CTR, DEPT SURG, DURHAM, NC 27710 USA
[4] DUKE UNIV, MED CTR, DEPT MED, DURHAM, NC 27710 USA
[5] DUKE UNIV, MED CTR, DEPT RADIOL, DURHAM, NC 27710 USA
[6] DUKE UNIV, MED CTR, DEPT PATHOL, DURHAM, NC 27710 USA
[7] DUKE UNIV, MED CTR, DEPT RADIAT ONCOL, DURHAM, NC 27710 USA
[8] UNIV KENTUCKY, DEPT PEDIAT, LOUISVILLE, KY USA
关键词
D O I
10.1016/S0002-9394(14)77408-2
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Trilateral retinoblastoma, the intracranial malignancy associated with bilateral retinoblastoma, is an uncommon and clinically aggressive malignancy with a uniformly fatal outcome. Three children with newly diagnosed trilateral retinoblastoma were treated with systemic (cyclophosphamide and vincristine) and intrathecal (methotrexate, hydrocortisone, and cytarabine) chemotherapy, as well as craniospinal irradiation (one patient) in addition to therapy of the eye lesions. All three patients have had partial or complete response of the pineal tumors to chemotherapy, with no active disease eight or more years, 33 or more months, and 12 or more months, respectively, after diagnosis of the lesions.
引用
收藏
页码:23 / 29
页数:7
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