[Alternative chemotherapy of malignant bone neoplasms in children].

Problemy medycyny wieku rozwojowego Pub Date : 1990-01-01
S Jurczyk-Procyk, D Perek
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Abstract

The authors propose alternative chemotherapy of osteosarcoma and Ewing's sarcoma in children. The aim of this proposal was elaboration of effective and, at the same time, less expensive and less toxic therapeutic regimens. The authors recommend open surgical biopsy with doxorubicin for 3 consecutive days as a protection against the released circulating neoplastic cells. After completion of histopathologic examination, one of two types of chemotherapy is chosen randomly. In osteosarcoma, there was induction chemotherapy for 4 or 9 weeks (according to the type of operation--conservative amputation or limb salvage surgery). In the I type of induction chemotherapy, high doses of methotrexate with vincristine and citrovorum factor rescue are administrated weekly, in the II type--the combination of BCD (bleomycin, cytoxan, actinomycin D) and CDDP (cisplatin). On the regimen of intensification chemotherapy decides the degree of tumour response to induction chemotherapy assessed as tumour necrosis in histopathologic examination. Maintenance chemotherapy is the same in two types of regimen and is continued for the period up to 2 years. The authors elaborated concomitantly the regimen of high methotrexate doses administration with rescue procedure in the case of elevated serum methotrexate levels, and regimen of cisplatin administration aiming at maximal patients protecting against the toxic effects of both drugs. In Ewing's sarcoma the randomisation differentiates between T-9 Rosen's regimen of chemotherapy and own modification of Memphis group regimen. The primary tumour is treated by radiotherapy with lower doses adjusted to the tumor response to induction chemotherapy (30-50 Gy or 50 Gy) and the irradiation port limited to the residual bone lesion plus a 2-3 centimeter margin. Surgical excision of bone with tumor depends on special tumor localisation as the clavicula, rib or fibula. The results of discussed treatment regimens will be subsequently published.

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儿童恶性骨肿瘤的替代化疗。
作者提出儿童骨肉瘤和尤文氏肉瘤的替代化疗方案。这项建议的目的是制订有效的、同时又较便宜和毒性较低的治疗方案。作者建议使用阿霉素连续3天进行开放性手术活检,以防止释放的循环肿瘤细胞。组织病理学检查完成后,随机选择两种化疗方案中的一种。骨肉瘤患者行诱导化疗4周或9周(根据手术类型-保守截肢或保肢手术)。在I型诱导化疗中,每周给予高剂量甲氨蝶呤与长春新碱和citrovorum因子拯救,II型- BCD(博来霉素,环磷酰胺,放线菌素D)和CDDP(顺铂)的组合。强化化疗方案决定肿瘤对诱导化疗的反应程度,组织病理学检查评价为肿瘤坏死。维持化疗在两种方案中是相同的,持续时间长达2年。作者同时阐述了在血清甲氨蝶呤水平升高的情况下,高剂量给药和抢救程序的方案,以及旨在最大限度地保护患者免受两种药物毒性作用的顺铂给药方案。在尤文氏肉瘤中,随机化区分了T-9 Rosen的化疗方案和自己修改的Memphis组方案。原发肿瘤采用放疗治疗,治疗剂量较低,以适应肿瘤对诱导化疗的反应(30-50 Gy或50 Gy),照射口限于残余骨病变加上2-3厘米的边缘。骨肿瘤的手术切除依赖于特殊的肿瘤定位,如锁骨、肋骨或腓骨。讨论的治疗方案的结果将随后发表。
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