Eichbaum Michael H R, Gast Anne-Sybil, Schneeweiss Andreas, Bruckner Thomas, Sohn Christof
Department of Gynecology and Obstetrics, University of Heidelberg Medical School, Heidelberg, Germany.
Am J Clin Oncol. 2007 Apr;30(2):139-45. doi: 10.1097/01.coc.0000251935.51345.10.
The aim of this retrospective study was to evaluate the activity and toxicity of a combined chemotherapy containing mitomycin, folinate, and 5-fluorouracil (MiFoFU) in patients with advanced metastatic breast cancer and reduced performance status, ie, elderly patients or heavily pretreated patients.
We studied the charts of 76 patients with progressive metastatic breast cancer who received MiFoFU chemotherapy at our institution between 1997 and 2003. Primary end points were response and time-to-progression (TTP); secondary end points were overall survival (OAS) and tolerability.
Median age was 57 years. Seventeen patients had > or =2 palliative cytostatic treatments before; 19 patients were older 65 years. Patients received a median of 6 cycles. Clinical benefit rate was 58%. After MiFoFU, median TTP and OAS were 8 months and 14 months, respectively. Main nonhematologic toxicity was stomatitis (grade I/II, 21%) and diarrhea (grade I/II, 37%). Grade III/IV hematotoxicity was seen in 18 patients (24%).
A combined MiFoFU chemotherapy is a well-tolerated treatment option in the palliative therapy for patients with metastatic breast cancer. In particular, the favorable efficacy/toxicity ratio in intensively pretreated or elderly patients makes this combination a reasonable alternative within these settings.
本回顾性研究旨在评估丝裂霉素、亚叶酸钙和5-氟尿嘧啶联合化疗(MiFoFU)对晚期转移性乳腺癌且体能状态较差患者(即老年患者或接受过大量治疗的患者)的活性及毒性。
我们研究了1997年至2003年间在我院接受MiFoFU化疗的76例转移性乳腺癌进展期患者的病历。主要终点为缓解率和疾病进展时间(TTP);次要终点为总生存期(OAS)和耐受性。
中位年龄为57岁。17例患者之前接受过≥2次姑息性细胞毒性治疗;19例患者年龄≥65岁。患者接受化疗的中位周期数为6个周期。临床获益率为58%。接受MiFoFU化疗后,中位TTP和OAS分别为8个月和14个月。主要非血液学毒性为口腔炎(Ⅰ/Ⅱ级,21%)和腹泻(Ⅰ/Ⅱ级,37%)。18例患者(24%)出现Ⅲ/Ⅳ级血液学毒性。
MiFoFU联合化疗是转移性乳腺癌患者姑息治疗中耐受性良好的治疗选择。特别是,在强化治疗或老年患者中,其良好的疗效/毒性比使该联合化疗在这些情况下成为合理的选择。