Chamberlain Marc C, Wei-Tsao Denice D, Blumenthal Deborah T, Glantz Michael J
Department of Neurology, University of Washington, Seattle, WA, USA.
Cancer. 2008 May 1;112(9):2038-45. doi: 10.1002/cncr.23404.
The primary objective of this prospective phase 2 study of CPT-11 in adult patients with recurrent temozolomide-refractory anaplastic astrocytoma (AA) was to evaluate 6-month progression-free survival (PFS).
Forty patients (27 men and 13 women) ages 17 to 58 years (median age, 38 years) with radiographically recurrent AA were treated. All patients had been treated previously with surgery, involved-field radiotherapy, and adjuvant chemotherapy. Fifteen patients were treated at first recurrence with an alternative chemotherapy. All patients were treated at either first or second recurrence with CPT-11 administered intravenously once every 3 weeks, which was defined operationally as a single cycle. Neurologic and neuroradiographic evaluations were performed every 9 weeks.
All patients were evaluable for toxicity, and 39 patients were evaluable for response. In total, 302 cycles of CPT-11 (median, 6 cycles; range, 1-22 cycles) were administered. CPT-11-related toxicity included diarrhea (19 cycles), leukopenia (16 cycles), fatigue (11 cycles), anemia (6 cycles), delayed nausea/vomiting (5 cycles), neutropenia (5 cycles), and renal failure (1 patient, 1 toxic death). Two patients (5%) patients required erythrocyte transfusions. Nine patients (23%) demonstrated a radiographic complete response (1 patient) or partial response (8 patients), 16 patients (41%) demonstrated stable disease, and 14 patients (36%) had progressive disease after 3 cycles of CPT-11. The median time to tumor progression was 4.1 month. The median survival was 6.9 months, and the 6-month and 12-month PFS rates were 40% and 5%, respectively.
CPT-11 demonstrated modest efficacy with acceptable toxicity in this cohort of adult patients with recurrent AA, all of whom had failed on prior temozolomide chemotherapy.
这项关于CPT - 11用于复发的、对替莫唑胺耐药的间变性星形细胞瘤(AA)成年患者的前瞻性2期研究的主要目标是评估6个月无进展生存期(PFS)。
对40例年龄在17至58岁(中位年龄38岁)、影像学检查显示为复发AA的患者(27例男性和13例女性)进行了治疗。所有患者此前均接受过手术、累及野放疗和辅助化疗。15例患者在首次复发时接受了替代化疗。所有患者在首次或第二次复发时接受CPT - 11治疗,每3周静脉注射1次,这在操作上被定义为1个周期。每9周进行一次神经学和神经影像学评估。
所有患者均可评估毒性,39例患者可评估反应。共给予302个周期的CPT - 11(中位值为6个周期;范围为1 - 22个周期)。与CPT - 11相关的毒性包括腹泻(19个周期)、白细胞减少(16个周期)、疲劳(11个周期)、贫血(6个周期)、延迟性恶心/呕吐(5个周期)、中性粒细胞减少(5个周期)以及肾衰竭(1例患者,1例毒性死亡)。2例患者(5%)需要输注红细胞。9例患者(23%)表现为影像学完全缓解(1例患者)或部分缓解(8例患者),16例患者(41%)疾病稳定,14例患者(36%)在接受3个周期的CPT - 11治疗后病情进展。肿瘤进展的中位时间为4.1个月。中位生存期为6.9个月,6个月和12个月的PFS率分别为40%和5%。
在这组复发AA的成年患者中,CPT - 11显示出适度疗效且毒性可接受,所有这些患者之前的替莫唑胺化疗均失败。