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首页> 外文期刊>癌と化学療法 >The safety of docetaxel with cyclophosphamide (TC) therapy as adjuvant chemotherapy for Japanese women with operable breast cancer
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The safety of docetaxel with cyclophosphamide (TC) therapy as adjuvant chemotherapy for Japanese women with operable breast cancer

机译:西紫杉醇与环磷酰胺(TC)治疗的安全性作为日本女性可操作乳腺癌的辅助化疗

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The safety of docetaxel (60 mg/m(2)) plus cyclophosphamide (600 mg/m(2)) every three weeks (TC) as adjuvant therapy for Japanese women with operable breast cancer was evaluated. Ehime TC Study Group initiated the randomized control study,which compared the effects of the TC course number (4 cycles versus 8 cycles) in the adjuvant setting on the treatment outcomes of breast cancer patients. Eight patients were investigated on the side effects of TC therapy, four of them were allocated to 4 cycles of TC, and four to eight cycles from May, 2004 to Feb. 2005. Leukocytopenia and neutropenia of grade 3 or 4 were seen in 50% and 63% of the cases, respectively. No febrile neutropenia was seen. Although the non-hematological side effects of grade 3 or 4 were not observed, alopecia, stomatitis, skin toxicities and edema of grade 2 were seen in 100%, 25%, 25%, 13% of cases, respectively. TC therapy was well tolerated. All anticancer drugs could be administered as scheduled. From these preliminary results, TC therapy seems to be able to be safely prescribed postoperatively for Japanese women operated for breast cancer.
机译:每三周(TC)为新紫杉醇(60mg / m(2))加上环磷酰胺(600mg / m(2))作为日本妇女可操作乳腺癌的辅助治疗。 ehime TC研究组启动了随机对照研究,该研究比较了TC路线数量(4个循环与8个循环)在乳腺癌患者治疗结果的辅助环境中的影响。在TC疗法的副作用中研究了八名患者,其中四个被分配给4个TC的循环,2004年5月至2005年5月的4至8个循环。白细胞病和3级或4级的中性蛋白酶率为50%分别为63%的病例。没有看到任何发热的中性粒细胞贫乏。虽然未观察到3级或4级或4级的非血液副作用,但分别在100%,25%,25%,13%的病例中观察到血症,口腔炎,皮肤毒性和水肿。 TC疗法耐受良好。所有抗癌药物都可以按计划进行。从这些初步结果来看,TC治疗似乎能够术后安全地开展用于乳腺癌的日本女性。

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