Suppr超能文献

缩短疗程间隔的大剂量环磷酰胺、表柔比星、长春新碱和泼尼松联合粒细胞集落刺激因子治疗非霍奇金淋巴瘤:一项II期研究

High-dose intensity cyclophosphamide, epidoxorubicin, vincristine and prednisone by shortened intervals and granulocyte colony-stimulating factor in non-Hodgkin's lymphoma: a phase II study.

作者信息

Pronzato P, Lionetto R, Botto F, Pensa F, Tognoni A

机构信息

Department of Medical Oncology, Ospedale S. Andrea, Loc Felettino, La Spezia, Italy.

出版信息

Br J Cancer. 1998 Sep;78(6):777-80. doi: 10.1038/bjc.1998.578.

Abstract

Twenty patients with non-Hodgkin's lymphoma were treated with a combination of cyclophosphamide (750 mg m(-2), day 1), epidoxorubicin (60 mg m(-2), day 1), vincristine (1.4 mg m(-2), day 1) and prednisone (100 mg m(-2), days 1-5) every 14 days. Shortening of intervals was associated with the prophylactic employment of granulocyte colony-stimulating factor (G-CSF; specifically, filgrastim) administered at a dose of 300 microg subcutaneously from day 6 to day 11. The ratio between actually delivered dose intensity and planned dose intensity was 1.0 in 18 out the 20 patients. Toxicity was acceptable; response rate and survival are in the expected range. The present study demonstrated the feasibility of acceleration of chemotherapy cycles to obtain dose intensification in non-Hodgkin's lymphoma.

摘要

20例非霍奇金淋巴瘤患者接受了环磷酰胺(750mg/m²,第1天)、表柔比星(60mg/m²,第1天)、长春新碱(1.4mg/m²,第1天)和泼尼松(100mg/m²,第1 - 5天)联合治疗,每14天重复一次。缩短治疗间隔与预防性使用粒细胞集落刺激因子(G - CSF;具体为非格司亭)有关,从第6天至第11天皮下注射,剂量为300μg。20例患者中有18例实际给予的剂量强度与计划剂量强度之比为1.0。毒性是可接受的;缓解率和生存率在预期范围内。本研究证明了在非霍奇金淋巴瘤中加速化疗周期以实现剂量强化的可行性。

相似文献

本文引用的文献

6
Are growth factors leukemogenic?
Leukemia. 1996 Jan;10(1):175-7.
9
A predictive model for aggressive non-Hodgkin's lymphoma.侵袭性非霍奇金淋巴瘤的预测模型。
N Engl J Med. 1993 Sep 30;329(14):987-94. doi: 10.1056/NEJM199309303291402.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验