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对于接受髓母细胞瘤治疗的幼儿,高剂量化疗后进行自体骨髓移植会取代颅脊髓照射吗?

Will high dose chemotherapy followed by autologous bone marrow transplantation supplant cranio-spinal irradiation in young children treated for medulloblastoma?

作者信息

Dupuis-Girod S, Hartmann O, Benhamou E, Doz F, Mechinaud F, Bouffet E, Coze C, Kalifa C

机构信息

Pediatrics Department, Institut Gustave Roussy, Villejuif, France.

出版信息

J Neurooncol. 1996 Jan;27(1):87-98. doi: 10.1007/BF00146088.

Abstract

UNLABELLED

Cranio-spinal irradiation is the gold standard treatment used in non metastatic medulloblastoma as prophylaxis against central nervous system (CNS) metastases. However, given the severe late effects caused by this procedure in children under 3 years of age, most pediatric oncologists are currently treating these patients with conventional chemotherapy in order to postpone or even avoid irradiation. In the French Society of Pediatric Oncology (SFOP) this attitude has been adopted since 1987. Among the patients treated without radiotherapy, 20 relapsed while on conventional chemotherapy and were entered in a study of high-dose chemotherapy (HDC) followed by ABMT. Their median age at diagnosis was 23 months (R5-71) and the relapse occurred at a median time of 6.3 months after the initiation of chemotherapy. Complete surgical removal of the local relapse was the first treatment in 4/20 patients who were not evaluable for response. Sixteen of the twenty patients had measurable disease at the primary site (9 patients), or at metastatic sites (3 patients) or both (4 patients). The conditioning regimen consisted of combination Busulfan 600 mg/m2 over 4 days and Thiotepa 900 mg/m2 over three days. After recovery from aplasia, patients with a local relapse received local radiotherapy limited to posterior fossa.

RESULTS

among the 16 patients with measurable disease, 6 CR, 6 PR, 3 NR, were observed following HDC (response rate 75%). One patient was not evaluable. For the 20 patients, the EFS is 50%. Among the surviving patients, the median follow up is 31 months post BMT (R12-82). Ten patients who developed a local relapse or local progression are alive with NED without craniospinal irradiation. Among the 7 patients who developed metastases or progression of metastases, only one is alive. Toxicity was high but manageable: the median duration of granulocytopenia < 0.5 x 109/l and thrombocytopenia < 50 x 10(9)/l was 13 and 41 days respectively. Bacteremia was documented in 4 cases. Grade > 2 mucositis and diarrhea were observed in 60% of patients. One complication-related death occurred 1 month post BMT.

CONCLUSION

With a 75% response rate, this HDC proved to be very efficient in relapsed medulloblastoma. A longer follow up is necessary to demonstrate whether, after a local relapse, HDC could replace craniospinal irradiation as prophylaxis against CNS metastases.

摘要

未标注

颅脊髓照射是用于非转移性髓母细胞瘤预防中枢神经系统(CNS)转移的金标准治疗方法。然而,鉴于该程序对3岁以下儿童会造成严重的晚期效应,目前大多数儿科肿瘤学家正在用传统化疗治疗这些患者,以推迟甚至避免照射。自1987年以来,法国儿科肿瘤学会(SFOP)一直采用这种态度。在未接受放疗的患者中,20例在接受传统化疗时复发,并进入了一项高剂量化疗(HDC)继以自体骨髓移植(ABMT)的研究。他们诊断时的中位年龄为23个月(范围5 - 71个月),复发发生在化疗开始后的中位时间6.3个月。4/20例患者对反应不可评估,其中局部复发的首次治疗是手术完全切除。20例患者中有16例在原发部位(9例患者)、转移部位(3例患者)或两者(4例患者)有可测量的疾病。预处理方案包括4天内给予白消安600mg/m²联合3天内给予噻替派900mg/m²。再生障碍恢复后,局部复发的患者接受限于后颅窝的局部放疗。

结果

在16例有可测量疾病的患者中,高剂量化疗后观察到6例完全缓解(CR)、6例部分缓解(PR)、3例疾病未缓解(NR)(缓解率75%)。1例患者不可评估。对于20例患者,无事件生存期(EFS)为50%。在存活患者中,自体骨髓移植后中位随访时间为31个月(范围12 - 82个月)。10例发生局部复发或局部进展的患者在未进行颅脊髓照射的情况下无疾病证据存活。在7例发生转移或转移进展的患者中,仅1例存活。毒性较高但可控制:粒细胞减少<0.5×10⁹/L和血小板减少<50×10⁹/L的中位持续时间分别为13天和41天。4例记录有菌血症。60%的患者观察到2级以上的粘膜炎和腹泻。1例与并发症相关的死亡发生在自体骨髓移植后1个月。

结论

高剂量化疗的缓解率为75%,在复发性髓母细胞瘤中被证明非常有效。需要更长时间的随访来证明在局部复发后,高剂量化疗是否可以替代颅脊髓照射作为预防中枢神经系统转移的方法。

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