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强化化疗联合干细胞支持——小儿实体瘤治疗经验

Intensive chemotherapy with stem cell support-experience in pediatric solid tumours.

作者信息

Pinkerton C R

机构信息

Royal Marsden NHS Trust, Sutton, Surrey, UK.

出版信息

Bull Cancer. 1995;82 Suppl 1:61s-65s.

PMID:7626856
Abstract

A recent Consensus Conference in Lyon reviewed the role of high-dose therapy with stem cell rescue in a variety of malignancies including childhood tumours. The conclusion was that with the exception of metastatic neuroblastoma there is still no proven role for this treatment strategy. It is more than 10 years since this approach was used in neuroblastoma and it has subsequently been applied to most of the common childhood solid tumours. Although a single randomised study has suggested that the progression-free survival is significantly prolonged with high-dose melphalan, the superiority of this over continued intensive conventional therapy is unclear. It seems likely that a selected subgroup of children with stage IV disease may benefit from megatherapy and the results of current randomised trials are awaited. In rhabdomyosarcoma, the duration of treatment may be shortened by dose escalation, but the impact on the outcome in very high-risk patients remains unproven. In Ewing's sarcoma, there has been difficulty defining high-risk patients, but recent studies suggest that megatherapy may have a role in patients with bone or bone marrow disease who have little chance of long-term survival with conventional chemotherapy approaches. In brain tumours, the results have been disappointing for gliomas, but there is currently enthusiasm about a possible role in the chemosensitive primitive neuroectodermal tumours. In this group of diseases which are inherently chemosensitive, the poor results from chemotherapy in the past have resulted from a failure to achieve appropriate drug levels at the tumour site and this may be potentially overcome by dose escalation. In Wilms' tumour, although the overall cure rate is very high, there appears to be a useful role for megatherapy in certain high-risk relapsed patients who have little chance of cure with conventional salvage therapy. There is an urgent need for international collaboration to design randomised studies which will as rapidly as possible address the issue of the role of these expensive and high morbidity procedures in childhood cancer.

摘要

最近在里昂召开的一次共识会议回顾了大剂量疗法联合干细胞救援在包括儿童肿瘤在内的多种恶性肿瘤中的作用。结论是,除转移性神经母细胞瘤外,这种治疗策略仍未得到证实。自这种方法应用于神经母细胞瘤以来已有10多年,随后它被应用于大多数常见的儿童实体瘤。尽管一项随机研究表明,大剂量美法仑可显著延长无进展生存期,但与持续强化的传统疗法相比,其优势尚不清楚。似乎IV期疾病的特定亚组儿童可能从大剂量疗法中获益,目前正在等待随机试验的结果。在横纹肌肉瘤中,剂量递增可能会缩短治疗时间,但对极高危患者预后的影响仍未得到证实。在尤因肉瘤中,很难定义高危患者,但最近的研究表明,大剂量疗法可能对那些采用传统化疗方法长期生存机会渺茫的骨或骨髓疾病患者有作用。在脑肿瘤中,胶质瘤的结果令人失望,但目前人们对其在对化疗敏感的原始神经外胚层肿瘤中可能发挥的作用充满热情。在这类本质上对化疗敏感的疾病中,过去化疗效果不佳是因为未能在肿瘤部位达到适当的药物水平,而这可能通过剂量递增得到潜在解决。在肾母细胞瘤中,尽管总体治愈率很高,但大剂量疗法在某些传统挽救疗法治愈机会渺茫的高危复发患者中似乎有一定作用。迫切需要开展国际合作来设计随机研究,以便尽快解决这些昂贵且高发病率的治疗方法在儿童癌症中的作用问题。

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