Ashley D M, Longee D, Tien R, Fuchs H, Graham M L, Kurtzberg J, Casey J, Olson J, Meier L, Ferrell L, Kerby T, Duncan-Brown M, Stewart E, Colvin O M, Pipas J M, McCowage G, McLendon R, Bigner D D, Friedman H S
Department of Pediatrics, Duke University Medical Center, Durham, NC 27710, USA.
Med Pediatr Oncol. 1996 Jun;26(6):387-92. doi: 10.1002/(SICI)1096-911X(199606)26:6<387::AID-MPO3>3.0.CO;2-D.
The outcome for patients with pineoblastoma has historically been very poor, with most patients dying of disseminated disease despite irradiation. Furthermore, the low incidence of this tumor has hindered progress toward defining better treatment strategies. Here we report the activity and toxicity of cyclophosphamide administered as a single agent at a dose schedule of 2 g/m2/day for 2 successive days at monthly intervals for a maximum of four courses. Eight patients were evaluated, six newly diagnosed and two recurrent. Amongst the six newly diagnosed patients, there were three patients demonstrating partial responses, and three had stable disease throughout the cyclophosphamide treatment period. All six patients are alive and disease free after further therapy. One patient with recurrent disease demonstrated tumor progression on cyclophosphamide, and the other had stable disease throughout the cyclophosphamide treatment period. Both patients subsequently died of progressive disease. The major toxicity of high dose cyclophosphamide was hematopoietic, with one patient requiring a dose reduction after three courses due to prolonged thrombocytopenia. One patient was also withdrawn from treatment with cyclophosphamide due to impaired pulmonary function. This study demonstrates the activity of high dose cyclophosphamide in the treatment of pineoblastoma and may serve as basis for the design of future studies of this tumor.
松果体母细胞瘤患者的历史预后一直很差,尽管接受了放疗,但大多数患者死于播散性疾病。此外,这种肿瘤的低发病率阻碍了在确定更好治疗策略方面取得进展。在此,我们报告了环磷酰胺作为单一药物的活性和毒性,给药方案为2 g/m²/天,连续2天,每月一次,最多四个疗程。对8例患者进行了评估,其中6例为新诊断患者,2例为复发性患者。在6例新诊断患者中,有3例患者出现部分缓解,3例在整个环磷酰胺治疗期间病情稳定。所有6例患者在进一步治疗后均存活且无疾病。1例复发性疾病患者在环磷酰胺治疗期间肿瘤进展,另1例在整个环磷酰胺治疗期间病情稳定。这两名患者随后均死于疾病进展。高剂量环磷酰胺的主要毒性是血液学毒性,1例患者因血小板减少持续时间过长,在三个疗程后需要减少剂量。1例患者也因肺功能受损而停止环磷酰胺治疗。本研究证明了高剂量环磷酰胺在松果体母细胞瘤治疗中的活性,可为该肿瘤未来研究的设计提供依据。