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采用拓扑异构酶-I抑制剂伊立替康(CPT-11)进行化疗,用于治疗难治性和复发性非霍奇金淋巴瘤。

Chemotherapy with irinotecan (CPT-11), a topoisomerase-I inhibitor, for refractory and relapsed non-Hodgkin's lymphoma.

作者信息

Takagi T, Saotome T

机构信息

Division of Laboratory Medicine, Chiba Cancer Center Hospital, Japan.

出版信息

Leuk Lymphoma. 2001 Aug;42(4):577-86. doi: 10.3109/10428190109099317.

DOI:10.3109/10428190109099317
PMID:11697485
Abstract

Irinotecan hydrochloride (CPT-11), a DNA topoisomerase-I inhibitor, is now widely used in the treatment of various solid tumors, including colorectal, gastric, breast, lung, and ovarian cancer. Despite the good response shown in the late phase-II study, CPT-11 was not often employed in the treatment of malignant lymphoma, mainly because of severe leukopenia and diarrhea caused by the recommended schedule: 40 mg/m2 of CPT-11 on days 1 to 3, 8 to 10, 15 to 17, then discontinued for at least 2 weeks. In clinical use, administration of CPT-11 had to be ceased on days 15 to 17 in almost all cases, and on days 8 to 10 in a considerable number of patients. Subsequently, a lower dose schedule (less than 40 mg/m2) was developed. Our phase II trial employing a reduced dose of CPT-11 on days 1 and 2, plus ADM on day 3 with 3-week interval in patients with refractory and relapsed NHL showed a fairly good response of relapsed B-cell lymphoma and a substantial response of T-cell lymphoma with acceptable toxicity. The combination of a topoisomerase-I inhibitor (CPT-11) and a topoisomerase-II inhibitor is an interesting concept for the treatment of NHL. Another phase II trial in combination with CPT-11 and other anti-cancer drugs, particularly cisplatin or topoisomerase-II inhibitors, is warranted. A superior salvage chemotherapy regimen could be found in the future by investigating combinations of low-dose CPT-11 and cisplatin or topoisomerase-II inhibitors.

摘要

盐酸伊立替康(CPT-11)是一种DNA拓扑异构酶I抑制剂,目前广泛应用于各种实体瘤的治疗,包括结直肠癌、胃癌、乳腺癌、肺癌和卵巢癌。尽管在II期后期研究中显示出良好的反应,但CPT-11并不常用于恶性淋巴瘤的治疗,主要是因为推荐方案(第1至3天、8至10天、15至17天给予40mg/m²的CPT-11,然后停药至少2周)会导致严重的白细胞减少和腹泻。在临床应用中,几乎所有病例在第15至17天必须停止使用CPT-11,相当一部分患者在第8至10天就不得不停药。随后,开发了一种较低剂量方案(低于40mg/m²)。我们对难治性和复发性非霍奇金淋巴瘤(NHL)患者进行的II期试验,在第1天和第2天采用降低剂量的CPT-11,第3天加用阿霉素,间隔3周,结果显示复发的B细胞淋巴瘤有相当好的反应,T细胞淋巴瘤有显著反应,且毒性可接受。拓扑异构酶I抑制剂(CPT-11)和拓扑异构酶II抑制剂联合应用是治疗NHL的一个有趣概念。有必要进行另一项将CPT-11与其他抗癌药物,特别是顺铂或拓扑异构酶II抑制剂联合应用的II期试验。通过研究低剂量CPT-11与顺铂或拓扑异构酶II抑制剂的联合应用,未来可能会找到一种更优的挽救化疗方案。

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