Dixon J M, Renshaw L, Bellamy C, Stuart M, Hoctin-Boes G, Miller W R
Edinburgh Breast Unit, Western General Hospital, Edinburgh, Scotland, United Kingdom.
Clin Cancer Res. 2000 Jun;6(6):2229-35.
Anastrozole, an orally active, nonsteroidal aromatase inhibitor, was evaluated in a randomized, double-blind, single-center study to determine its efficacy as neoadjuvant therapy in postmenopausal women with newly diagnosed, estrogen receptor-rich, locally advanced or large (>3 cm), operable breast cancers. Twenty-four eligible patients were recruited into the study and received either 1 mg (n = 12) or 10 mg (n = 12) of anastrozole daily over a 3-month period. Tumor volumes were estimated clinically, by using caliper measurements and ultrasound (at baseline and after 1, 2, and 3 months' treatment) and by mammography (at baseline and after 3 months). Tumor volume was also measured in surgical specimens. Twenty-one patients were classified as T2, two patients as T3, and one patient as T4B at baseline. Three patients had clinical evidence of lymph node involvement. When considering the difference between the volume as measured by each assessment and the actual pathological volume, the interquartile range and the difference between the maximum and minimum values were smaller for ultrasound when compared with those measured with calipers and mammography. Therefore, of the three clinical assessments of tumor volume used in this study, the data suggest that ultrasound may be the most accurate. The median reductions in tumor volumes as measured by ultrasound for those patients with a measurable 12-week assessment were 80.5 and 69.6% for anastrozole (1 and 10 mg, respectively) after 12 weeks of treatment and 75.5% when both doses were grouped together. Moreover, of these patients, 11 of 12 given 1 mg and 7 of 11 given 10 mg of anastrozole were found on ultrasound to have a >50% reduction in tumor volume after 12 weeks of treatment. Of the 17 patients who would have required a mastectomy at initiation of treatment, 15 were suitable for breast conservation after anastrozole treatment. These results suggest that anastrozole is highly effective as neoadjuvant therapy in postmenopausal women with estrogen receptor-rich, large, operable breast cancer. Future studies comparing anastrozole with tamoxifen as a neoadjuvant treatment should be considered.
阿那曲唑是一种口服活性非甾体芳香酶抑制剂,在一项随机、双盲、单中心研究中对其进行了评估,以确定其作为新辅助治疗药物,用于治疗新诊断的、雌激素受体丰富、局部晚期或体积较大(>3 cm)且可手术的绝经后乳腺癌女性患者的疗效。24名符合条件的患者被纳入该研究,并在3个月的时间里每日接受1 mg(n = 12)或10 mg(n = 12)的阿那曲唑治疗。通过使用卡尺测量和超声检查(在基线以及治疗1、2和3个月后)以及乳房X线摄影(在基线和3个月后)对肿瘤体积进行临床评估。还在手术标本中测量肿瘤体积。基线时,21例患者被分类为T2期,2例患者为T3期,1例患者为T4B期。3例患者有淋巴结受累的临床证据。在考虑每种评估方法测量的体积与实际病理体积之间的差异时,与用卡尺和乳房X线摄影测量的结果相比,超声测量的四分位间距以及最大值与最小值之间的差异更小。因此,在本研究中使用的三种肿瘤体积临床评估方法中,数据表明超声可能是最准确的。对于那些在12周评估时可测量的患者,经超声测量,阿那曲唑(分别为1 mg和10 mg)治疗12周后肿瘤体积的中位数减少率分别为80.5%和69.6%,两种剂量合并计算时为75.5%。此外,在这些患者中,接受1 mg阿那曲唑治疗的12例患者中有11例、接受10 mg阿那曲唑治疗的11例患者中有7例在超声检查中显示治疗12周后肿瘤体积减少>50%。在治疗开始时需要进行乳房切除术的17例患者中,15例在阿那曲唑治疗后适合保乳手术。这些结果表明,阿那曲唑作为新辅助治疗药物,对于雌激素受体丰富、体积较大且可手术的绝经后乳腺癌女性患者具有高效性。应考虑开展未来研究,将阿那曲唑与他莫昔芬作为新辅助治疗药物进行比较。