Stomper P C, Gelman R S
Dana-Farber Cancer Institute, Boston, Massachusetts.
Hematol Oncol Clin North Am. 1989 Dec;3(4):611-40.
It is now generally accepted that screening mammography at 1- to 3-year intervals can decrease mortality from breast cancer. Three randomized trials, involving a total of 238,000 women, have reported mortality results. In two trials (HIP and S2C), there was a significant reduction in breast cancer mortality (22 per cent at 18 years and 27 per cent at 8 years). One trial (Mälmo) showed a nonsignificant reduction in mortality at year 9 (5 per cent) and nonsignificant increases in mortality at earlier years. There are little data from randomized trials to support a benefit of mammographic screening in women under 50 years old. The two Swedish studies at last follow-up had 26 and 29 per cent more breast cancer deaths in young women in the group randomized to screening. The HIP study had 25 per cent fewer breast cancer deaths at 18 years in women under age 50 at the start of the trial, but because only 12 patients under age 50 had mammographically detectable tumors (out of 89 cancers diagnosed in the screened group), most of the benefit must be due to physical examinations or increased awareness of breast cancer symptoms. The as yet unpublished results of the Canadian trial in women under age 50 should elucidate the benefit of mammography in this age group. American centers report a malignant biopsy rate of 20 to 30 per cent for clinically occult lesions. This rate should increase as the proportion of women who have had prior mammography increases. High-quality mammography, including magnification technique for evaluation of suspicious lesions, proper localization and excisional biopsy techniques with pathologic correlation, and potentially, fine-needle aspiration, may improve the yield of screening mammography-induced open-biopsy procedures. Magnification technique can improve mammographic assessment of the extent of the tumor and guide re-excision for patients being considered for breast-conserving therapy. In the irradiated breast, in our experience, mammography alone detected 35 per cent of recurrent cancers in the irradiated breast. We recommend routine mammographic follow-up of the irradiated breast, including magnification of the local excision site, at 6 months, 1 year, and annually thereafter.
目前普遍认为,每隔1至3年进行一次乳腺钼靶筛查可降低乳腺癌死亡率。三项随机试验,共涉及238,000名女性,报告了死亡率结果。在两项试验(HIP和S2C)中,乳腺癌死亡率显著降低(18年时降低22%,8年时降低27%)。一项试验(马尔默)显示,第9年死亡率有不显著降低(5%),而在早期死亡率有不显著升高。随机试验几乎没有数据支持对50岁以下女性进行乳腺钼靶筛查有益。瑞典的两项研究在最后随访时发现,随机分配到筛查组的年轻女性乳腺癌死亡人数多26%和29%。HIP研究中,试验开始时年龄在50岁以下的女性在18年时乳腺癌死亡人数少25%,但由于筛查组中诊断出的89例癌症中,只有12例50岁以下患者的肿瘤可通过乳腺钼靶检测到,所以大部分益处肯定归因于体格检查或对乳腺癌症状的认识提高。加拿大对50岁以下女性进行的试验尚未公布的结果应能阐明该年龄组乳腺钼靶筛查的益处。美国各中心报告,临床隐匿性病变的恶性活检率为20%至30%。随着接受过乳腺钼靶检查的女性比例增加,这一比率应该会上升。高质量的乳腺钼靶检查,包括用于评估可疑病变的放大技术、适当的定位和切除活检技术以及病理相关性,还有可能包括细针穿刺抽吸,可能会提高乳腺钼靶筛查引发的开放活检程序的检出率。放大技术可以改善对肿瘤范围的乳腺钼靶评估,并指导考虑保乳治疗的患者进行再次切除。根据我们的经验,在接受放疗的乳房中,仅乳腺钼靶检查就检测出35%的放疗后复发性癌症。我们建议对接受放疗的乳房进行常规乳腺钼靶随访,包括在6个月、1年时以及此后每年对局部切除部位进行放大检查。