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南美洲采用大剂量化疗和自体干细胞解救成功治疗转移性视网膜母细胞瘤。

Successful treatment of metastatic retinoblastoma with high-dose chemotherapy and autologous stem cell rescue in South America.

机构信息

Bone Marrow Transplantation Unit, Hospital Calvo Mackenna, Santiago, Chile.

出版信息

Bone Marrow Transplant. 2012 Apr;47(4):522-7. doi: 10.1038/bmt.2011.108. Epub 2011 May 23.

Abstract

High-dose chemotherapy (HDC) followed by autologous stem cell rescue (ASCR) is the only curative treatment for metastatic retinoblastoma, but its feasibility in developing countries is unknown. We report 11 consecutive children (six unilateral) treated in three South-American middle-income countries with HDC-ASCR. One patient had metastatic retinoblastoma at diagnosis and the remaining ones had a metastatic relapse. Metastatic sites included BM=6, bone=4, orbit=5 and central nervous system (CNS)=4. All patients received induction with conventional chemotherapy achieving CR at a median of 5.7 months from the diagnosis of metastasis. Conditioning regimens included carboplatin and etoposide with thiotepa in six or with CY in four or melphalan in one patient. All patients engrafted after G-CSF-mobilized peripheral blood ASCR and no toxic deaths occurred. Two children received post-ASCR CNS radiotherapy. Seven children have disease-free survival (median follow-up 39 months). CNS relapse, isolated (n=3) or with systemic relapse (n=1), occurring at a median of 7 months after ASCT was the most common event. In the same period, five children with metastatic retinoblastoma did not qualify for HDC-ASCR and died. We conclude that HDC-ASCR is a feasible and effective treatment for children with metastatic retinoblastoma in middle-income countries.

摘要

大剂量化疗(HDC)继自体干细胞解救(ASCR)是治疗转移性视网膜母细胞瘤的唯一根治性治疗方法,但在发展中国家的可行性尚不清楚。我们报告了三个南美中等收入国家的 11 例连续儿童(6 例单侧)接受 HDC-ASCR 治疗的情况。1 例患者在诊断时即患有转移性视网膜母细胞瘤,其余患者均有转移性复发。转移部位包括骨髓=6、骨骼=4、眼眶=5 和中枢神经系统(CNS)=4。所有患者均接受常规化疗诱导,在诊断转移后中位数为 5.7 个月达到完全缓解。预处理方案包括卡铂和依托泊苷联合噻替哌 6 例,或联合环磷酰胺 4 例,或美法仑 1 例。所有患者在 G-CSF 动员外周血 ASCR 后均植入成功,无毒性死亡。2 例患儿接受了 ASCR 后中枢神经系统放疗。7 例患儿无疾病生存(中位随访 39 个月)。CNS 复发是最常见的事件,孤立性(n=3)或伴系统性复发(n=1),发生在 ASCT 后中位数为 7 个月。同期,5 例患有转移性视网膜母细胞瘤的患儿不符合 HDC-ASCR 条件,死亡。我们得出结论,HDC-ASCR 是中低收入国家儿童转移性视网膜母细胞瘤的一种可行且有效的治疗方法。

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