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以剂量密集表柔比星进行FEC化疗作为高危乳腺癌初始治疗的可行性研究

Feasibility study of FEC-chemotherapy with dose-intensive epirubicin as initial treatment in high-risk breast cancer.

作者信息

van der Wall E, Richel D J, Kusumanto Y H, Rutgers E J, Schornagel J H, Schaake-Koning C C, Peterse J L, Rodenhuis S

机构信息

Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam.

出版信息

Ann Oncol. 1993 Nov;4(9):791-2. doi: 10.1093/oxfordjournals.annonc.a058667.

Abstract

BACKGROUND

The prognosis of patients with stage III B breast carcinoma with metastasis to the apical axillary lymph nodes is poor despite adequate local control achieved by surgery and/or radiation therapy. This study evaluated the feasibility of a dose-intensive up-front chemotherapy regimen in this subgroup of patients.

PATIENTS AND METHODS

A preoperative chemotherapy regimen consisting of 3 courses of fluorouracil 500 mg/m2, dose-intensive epidoxorubicin 120 mg/m2 and cyclophosphamide 500 mg/m2 (DIE-FEC), was administered at 21-day intervals without hematopoietic growth factors to 31 patients with apex-positive disease. All patients were below 60 years of age and none had had prior chemotherapy or radiotherapy.

RESULTS

Seven patients achieved clinical complete responses (23%), and 21 achieved clinical partial responses (68%); three patients had stable disease (10%), one of whom had only ductal carcinoma in situ at histopathologic evaluation, which suggested an additional response to therapy. The major toxicity was moderate bone marrow suppression with a median WBC nadir of 1650/microliters (range 500-4600). Other toxic effects were mild.

CONCLUSION

DIE-FEC is well-tolerated and highly effective as up-front chemotherapy in relatively young patients with high-risk breast cancer, with a 90% (CI 74%-98%) clinical objective response rate.

摘要

背景

尽管通过手术和/或放射治疗实现了充分的局部控制,但伴有腋窝尖淋巴结转移的ⅢB期乳腺癌患者的预后仍然很差。本研究评估了在该亚组患者中采用剂量密集型一线化疗方案的可行性。

患者与方法

对31例腋窝尖淋巴结阳性的患者,每21天给予一个术前化疗方案,该方案由3个疗程组成,包括氟尿嘧啶500mg/m²、剂量密集型表柔比星120mg/m²和环磷酰胺500mg/m²(DIE-FEC),且不使用造血生长因子。所有患者年龄均在60岁以下,且均未接受过先前的化疗或放疗。

结果

7例患者达到临床完全缓解(23%),21例达到临床部分缓解(68%);3例患者病情稳定(10%),其中1例在组织病理学评估时仅为原位导管癌,这提示对治疗有额外反应。主要毒性为中度骨髓抑制,白细胞计数最低点中位数为1650/微升(范围500-4600)。其他毒性作用较轻。

结论

DIE-FEC作为相对年轻的高危乳腺癌患者的一线化疗方案耐受性良好且高效,临床客观缓解率为90%(可信区间74%-98%)。

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