Department of Radiology, Institut de Cancérologie de Lorraine Alexis Vautrin, Vandœuvre-lès-Nancy, France.
Department of Radiology, Institut Bergonié, Bordeaux, France.
JAMA Intern Med. 2019 Mar 1;179(3):407-414. doi: 10.1001/jamainternmed.2018.7169.
Many women dread undergoing mammography, and some may not attend or reattend breast cancer screening because of the discomfort or pain induced by breast compression.
To evaluate the noninferiority of the self-compression mammography technique for reducing breast thickness compared with standard compression.
DESIGN, SETTING, AND PARTICIPANTS: This prospective, parallel-group, noninferiority randomized clinical trial was conducted from May 7, 2013, to October 26, 2015, at 6 cancer care centers in France. Participants were women aged 50 to 75 years, without a history of recent breast surgical procedure or treatment, and who could perform self-compression. Analyses were performed on intention-to-treat basis from January 27, 2017, to March 30, 2018.
Patients were randomized 1:1 to the self-compression group or the standard compression group.
Primary end point was breast thickness expressed as the mean of 4 views: right and left craniocaudal and right and left mediolateral oblique. The predefined noninferiority margin was a difference of 3 mm, with a 1-sided 95% CI. Secondary end points included compression force, image quality, requirement for additional views, pain, and patient satisfaction and radiographer assessment questionnaires.
Among the 549 women randomized, 548 (97.3%) completed the trial. Of these, 275 (48.8%) (mean [SD] age, 61.35 [6.34] years) were randomized to the self-compression arm and 273 (48.5%) (mean [SD] age, 60.84 [6.41] years) to the standard compression arm. The difference in the mean thickness between the 2 arms was lower than the noninferiority margin, with an upper 1-sided 95% CI less than 3 mm (-0.17; 95% CI,-∞ to 1.89 mm; P < .05). Compression force was higher in the self-compression group compared with the standard compression arm for the 4 mammographic views. Pain was statistically significantly lower in the self-compression group (n = 274) compared with the standard compression group (n = 269) (median [interquartile range (IQR)] score, 2 [1-5] vs 3 [1-5]; P = .009). No difference was reported in the image quality scores of the 2 groups or in the number of additional views performed (median [IQR] extra views, 2 [2-2] vs 2 [2-3] extra views; P = .64), whatever the indication, including insufficient image quality (29 [16.8%] vs 27 [15.0%] insufficient quality views; P = .65). No adverse effects or pain were reported by the participants after the self-compression mammography.
Self-compression does not appear to be inferior to standard compression mammography in achieving minimal breast thickness without increasing pain or compromising image quality; this technique may be an effective option for women who want to be involved in their breast examination.
ClinicalTrials.gov identifier: NCT02866591.
许多女性害怕接受乳房 X 光检查,由于乳房压迫引起的不适或疼痛,一些女性可能不会或重新参加乳腺癌筛查。
评估自我压缩乳房 X 光技术与标准压缩相比减少乳房厚度的非劣效性。
设计、设置和参与者:这项前瞻性、平行组、非劣效性随机临床试验于 2013 年 5 月 7 日至 2015 年 10 月 26 日在法国的 6 家癌症护理中心进行。参与者为年龄在 50 岁至 75 岁之间、没有近期乳房手术或治疗史且能够进行自我压缩的女性。分析是基于意向治疗的,从 2017 年 1 月 27 日到 2018 年 3 月 30 日进行。
患者被随机分为 1:1 的自我压缩组或标准压缩组。
主要终点是 4 个视图的乳房厚度平均值:右侧和左侧头尾向和右侧和左侧内外斜向。预设的非劣效性边界为 3 毫米,单侧 95%置信区间。次要终点包括压缩力、图像质量、需要额外的视图、疼痛以及患者满意度和放射技师评估问卷。
在随机分配的 549 名女性中,548 名(97.3%)完成了试验。其中,275 名(48.8%)(平均[SD]年龄,61.35[6.34]岁)被随机分配到自我压缩组,273 名(48.5%)(平均[SD]年龄,60.84[6.41]岁)被随机分配到标准压缩组。2 组间平均厚度的差异低于非劣效性边界,单侧 95%置信区间上限小于 3 毫米(-0.17;95%CI,-∞至 1.89 毫米;P<0.05)。与标准压缩组相比,自我压缩组在 4 个乳房 X 光视图中的压缩力更高。自我压缩组(n=274)的疼痛明显低于标准压缩组(n=269)(中位数[四分位数范围(IQR)]评分,2[1-5]比 3[1-5];P=0.009)。无论适应症如何,包括图像质量不足(29[16.8%]与 27[15.0%]图像质量不足视图;P=0.65),2 组的图像质量评分或额外视图数量均无差异(中位数[IQR]额外视图,2[2-2]比 2[2-3]额外视图;P=0.64)。无论哪种情况,参与者在接受自我压缩乳房 X 光检查后都没有报告任何不良反应或疼痛。
自我压缩在不增加疼痛或影响图像质量的情况下,似乎与标准压缩乳房 X 光检查一样无法达到最小的乳房厚度;对于希望参与乳房检查的女性来说,这种技术可能是一种有效的选择。
ClinicalTrials.gov 标识符:NCT02866591。