Lavrenkov Konstantin, Man Sofia, Geffen David B, Cohen Yoram
Department of Oncology, Soroka University Medical Center, Beer Sheva, Israel.
Isr Med Assoc J. 2002 Mar;4(3):176-7.
Recent years have brought significant progress to the development of hormonal therapies for the treatment of breast cancer. Several new agents have been approved for the treatment of breast cancer in the metastatic setting, among which is the new non-steroidal aromatase inhibitor, anastrozole, introduced for clinical use in Israel in March 1997.
To evaluate the response rate and survival duration of patients treated with anastrozole for metastatic breast cancer, who had previously received at least one line of hormonal therapy.
Anastrozole was administered to 37 patients with metastatic breast cancer. The median age was 64 years. Estrogen receptor was positive in 20 patients, negative in 10 and unknown in 7. All patients were previously treated with tamoxifen in the adjuvant setting or as first-line hormonal therapy for metastatic disease. Anastrozole was given orally, 1 mg/day. Response was evaluated 2 months after the initiation of treatment and reevaluated every 2 months. Therapy was given until disease progression. Ten ER-negative patients were excluded from the final analysis.
Twenty-seven patients were eligible for response and toxicity analysis. The median follow-up was 20 months. One patient (3.7%) achieved complete response and remains free of disease 28 months after start of therapy. No partial responses were seen. Twenty patients (74%) had stable disease. Two year actuarial survival was 57%. Median survival was 26.5 months after starting therapy and median progression-free survival was 11 months. The toxicity was mild: one patient (3.7%) complained of weight gain and one patient (3.7%) had mild fatigue.
Although the response rate was low, hormonal therapy with anastrozole seems to be beneficial in terms of disease stabilization, freedom from progression, and overall survival without serious toxicity.
近年来,乳腺癌激素治疗的发展取得了重大进展。几种新药物已被批准用于治疗转移性乳腺癌,其中包括新型非甾体芳香酶抑制剂阿那曲唑,于1997年3月在以色列投入临床使用。
评估先前接受过至少一线激素治疗的转移性乳腺癌患者使用阿那曲唑治疗的缓解率和生存期。
对37例转移性乳腺癌患者给予阿那曲唑治疗。中位年龄为64岁。雌激素受体阳性20例,阴性10例,未知7例。所有患者先前均在辅助治疗中或作为转移性疾病的一线激素治疗接受过他莫昔芬治疗。阿那曲唑口服给药,1毫克/天。治疗开始2个月后评估缓解情况,每2个月重新评估一次。治疗持续至疾病进展。10例雌激素受体阴性患者被排除在最终分析之外。
27例患者符合缓解和毒性分析标准。中位随访时间为20个月。1例患者(3.7%)达到完全缓解,在治疗开始后28个月仍无疾病。未观察到部分缓解。20例患者(74%)疾病稳定。两年精算生存率为57%。开始治疗后的中位生存期为26.5个月,中位无进展生存期为11个月。毒性轻微:1例患者(3.7%)抱怨体重增加,1例患者(3.7%)有轻度疲劳。
尽管缓解率较低,但阿那曲唑激素治疗在疾病稳定、无进展和总体生存方面似乎有益,且无严重毒性。