Salem Dina A, Gado Nevine M, Abdelaziz Nashwa N, Essa Ahmed E, Abdelhafeez Zeinab M, Kamel Tarek H
The Department of Radiation Oncology, Ain Shams University.
J Egypt Natl Canc Inst. 2008 Jun;20(2):134-40.
To evaluate the efficacy and tolerability of metronomic chemotherapy (which is the continuous administration of chemotherapy at relatively low minimally toxic doses on a frequent schedule of administration at close regular intervals with no prolonged drug-free breaks) in metastatic breast cancer patients as salvage therapy.
In this phase II study we evaluated the clinical efficacy and tolerability of low dose, oral Methotrexate (MTX) and Cyclophosphamide (CTX) in patients with metastatic breast cancer. Between January 2004 and December 2005, 42 patients received MTX 2.5mg bid on day 1 and 2 each week and CTX 50mg/day administered continuously.
Forty two patients were evaluable. The overall clinical benefit was 31% complete response, partial response and stable disease (CR+PR+SD >or=24 weeks), while the overall response rate was 16.7% (none of the patients attained CR). Toxicity was generally mild. The most common non hematological toxicity was elevation in transaminases level, it was reported in 40.4% of patients and was reversible, while mild grade 1 or 2 neutropenia was the most common hematological toxicity, (28.5% of patients). Median time to response was 3+/-0.18 while progression free survival (PFS) among patients with clinical benefit was 10 months (95% CI 6.65-13.44).
This phase II study shows that, the combination of continuously low dose MTX and CTX is an active minimally toxic and significantly cost effective regimen for the treatment of metastatic breast cancer patients.
评估节拍化疗(即连续给予相对低的最小毒性剂量化疗药物,给药频率高、间隔规律,无长时间无药间期)作为挽救疗法对转移性乳腺癌患者的疗效和耐受性。
在这项II期研究中,我们评估了低剂量口服甲氨蝶呤(MTX)和环磷酰胺(CTX)对转移性乳腺癌患者的临床疗效和耐受性。2004年1月至2005年12月期间,42例患者每周第1天和第2天接受MTX 2.5mg,每日两次,CTX 50mg/天持续给药。
42例患者可评估。总体临床获益为31%(完全缓解、部分缓解和疾病稳定,CR+PR+SD≥24周),而总体缓解率为16.7%(无患者达到CR)。毒性一般较轻。最常见的非血液学毒性是转氨酶水平升高,40.4%的患者出现该情况且可逆转,而轻度1级或2级中性粒细胞减少是最常见的血液学毒性(28.5%的患者)。中位缓解时间为3±0.18,临床获益患者的无进展生存期(PFS)为10个月(95%CI 6.65 - 13.44)。
这项II期研究表明,持续低剂量MTX和CTX联合方案是治疗转移性乳腺癌患者的一种有效、毒性最小且成本效益显著的方案。