Tominaga T, Kimura M, Toge T, Takashima S, Nomura Y, Ohashi Y
Breast Cancer Center, Toyosu Hospital, Showa University School of Medicine.
Gan To Kagaku Ryoho. 2000 Oct;27(11):1709-18.
To elucidate the combined effects of fadrozole (nonsteroidal aromatase inhibitor) and tamoxifen, 11 postmenopausal patients with recurrent breast cancer were examined between October 1996 and June 1998. One patient, 49 years old, was ineligible due to the short period after castration. The patients were aged 53-71 years (mean 63.5). PS was 0-1. Six patients were pre-treated with tamoxifen and 6 with oral 5-FU derivatives. One had no previous treatment. The target lesions were soft tissues in 5, bone in 4, lungs in 6 and liver in 1. The response was CR in 2, PR in 2, SD (longer than 24 weeks) in 2, NC in 1 and PD in 3. Consequently, the response rate was 60% (6 out of 10 eligible cases). Hormonal concentration was measured before and after administration of two drugs in weeks 2, 4, 6, 8 and at the end of the treatment, and significant decreases in estrogens in peripheral blood were observed. Adverse effects (4 cases of low grade headache, dizziness and elevation of GOT, GPT, gamma-GTP) did not influence the continuous administration of the drugs. We conclude that combined administration of fadrozole (2nd generation aromatase inhibitor) and tamoxifen produces a good response in postmenopausal recurrent breast cancer patients, and can be a useful treatment for patients with breast cancer.
为阐明法倔唑(非甾体类芳香化酶抑制剂)与他莫昔芬的联合疗效,于1996年10月至1998年6月期间对11例绝经后复发性乳腺癌患者进行了研究。1例49岁患者因去势后时间较短而不符合条件。患者年龄为53 - 71岁(平均63.5岁)。体能状态为0 - 1级。6例患者曾接受他莫昔芬预处理,6例曾接受口服5 - 氟尿嘧啶衍生物治疗。1例未曾接受过治疗。靶病灶位于软组织的有5例,骨的有4例,肺的有6例,肝的有1例。疗效为完全缓解(CR)2例,部分缓解(PR)2例,疾病稳定(SD,超过24周)2例,疾病无变化(NC)1例,疾病进展(PD)3例。因此,缓解率为60%(10例符合条件的病例中有6例)。在第2、4、6、8周及治疗结束时测定了两种药物给药前后的激素浓度,观察到外周血雌激素显著下降。不良反应(4例出现轻度头痛、头晕及谷草转氨酶、谷丙转氨酶、γ-谷氨酰转肽酶升高)未影响药物的持续使用。我们得出结论,法倔唑(第二代芳香化酶抑制剂)与他莫昔芬联合给药对绝经后复发性乳腺癌患者产生了良好疗效,可作为乳腺癌患者的一种有效治疗方法。