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额外的化疗药物可改善晚期B细胞淋巴瘤儿童和成人的治疗效果。

Additional chemotherapy agents improve treatment outcome for children and adults with advanced B-cell lymphomas.

作者信息

Adde M, Shad A, Venzon D, Arndt C, Gootenberg J, Neely J, Nieder M, Owen W, Seibel N, Wilson W, Horak I D, Magrath I

机构信息

Division of Clinical Sciences, National Cancer Institute, Bethesda, MD 20892, USA.

出版信息

Semin Oncol. 1998 Apr;25(2 Suppl 4):33-9; discussion 45-8.

PMID:9578060
Abstract

We report the updated results of an intensive treatment protocol for children (< 18 years) and adults (> or = 18 years) with advanced B-cell lymphomas. The protocol consists of two chemotherapy regimens: A, consisting of cyclophosphamide, doxorubicin, vincristine and high-dose methotrexate (CODOX-M), and B, consisting of ifosfamide, etoposide, and high-dose cytarabine (IVAC). Both cycles included intrathecal chemotherapy (cytarabine or methotrexate). Patients received a total of four cycles in the following sequence: A, B, A, B. Sixty-six previously untreated patients, enrolled before October 1996, were included in the present analysis. Of these, 55 had Burkitt's or Burkitt's-like lymphoma and 11 had diffuse large B-cell lymphoma. There were 53 males ad 13 females; 40 were children and 26 were adults (age range, 3 to 57 years). To date, 61 patients have achieved a complete response to therapy. Two patients subsequently relapsed, but one of these is a long-term survivor after further therapy and a bone marrow transplant. The event-free survival rate is 85% at I year and beyond. The median potential follow-up period is 48 months (range, 12 to 96 months) for patients remaining in complete remission. Neutropenia occurred in 98% of cycles and infection in 46% of A cycles and 50% of B cycles, but the duration was shortened in B cycles by the administration of granulocyte colony-stimulating factor. Positive blood cultures were observed in 21% of A cycles and 28% of B cycles, and there have been three toxic deaths. These results are better than those achieved with an earlier version of CODOX-M, suggesting that the addition of the IVAC regimen is responsible for the improved results. The similarity of the outcome in children and adults, however, confirms our previous observation that, at least in adults younger than 60 years with Burkitt's or Burkitt's-like lymphomas, treatment with regimens similar to those used in children is warranted.

摘要

我们报告了针对患有晚期B细胞淋巴瘤的儿童(<18岁)和成人(≥18岁)的强化治疗方案的更新结果。该方案由两种化疗方案组成:方案A,由环磷酰胺、阿霉素、长春新碱和大剂量甲氨蝶呤(CODOX-M)组成;方案B,由异环磷酰胺、依托泊苷和大剂量阿糖胞苷(IVAC)组成。两个周期均包括鞘内化疗(阿糖胞苷或甲氨蝶呤)。患者按以下顺序共接受四个周期的治疗:A、B、A、B。本分析纳入了1996年10月之前入组的66例既往未接受过治疗的患者。其中,55例患有伯基特淋巴瘤或伯基特样淋巴瘤,11例患有弥漫性大B细胞淋巴瘤。有53名男性和13名女性;40例为儿童,26例为成人(年龄范围为3至57岁)。迄今为止,61例患者已实现对治疗的完全缓解。两名患者随后复发,但其中一名在进一步治疗和骨髓移植后成为长期幸存者。1年及以后的无事件生存率为85%。对于仍处于完全缓解状态的患者,中位潜在随访期为48个月(范围为12至96个月)。98%的周期出现中性粒细胞减少,方案A周期的46%和方案B周期的50%出现感染,但通过给予粒细胞集落刺激因子,方案B周期的持续时间缩短。方案A周期的21%和方案B周期的28%观察到血培养阳性,并且有三例毒性死亡。这些结果优于早期版本的CODOX-M所取得的结果,表明添加IVAC方案是结果改善的原因。然而,儿童和成人结果的相似性证实了我们之前的观察,即至少在年龄小于60岁的患有伯基特淋巴瘤或伯基特样淋巴瘤的成人中,采用与儿童相似的方案进行治疗是合理的。

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