Department of Clinical Science and Education at Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
Department of Oncology, Södersjukhuset, Stockholm, Sweden.
Breast Cancer Res Treat. 2021 Dec;190(3):451-462. doi: 10.1007/s10549-021-06386-2. Epub 2021 Sep 27.
Change in mammographic density has been suggested to be a proxy of tamoxifen response. We investigated the effect of additional adjuvant systemic therapy and CYP2D6 activity on MD change in a cohort of tamoxifen-treated pre- and postmenopausal breast cancer patients.
Swedish breast cancer patients (n = 699) operated 2006-2014, genotyped for CYP2D6, having at least three months postoperative tamoxifen treatment, a baseline, and at least one follow-up digital mammogram were included in the study. Other systemic adjuvant treatment included chemotherapy, goserelin, and aromatase inhibitors. Change in MD, dense area, was assessed using the automated STRATUS method. Patients were stratified on baseline characteristics, treatments, and CYP2D6 activity (poor, intermediate, extensive, and ultrarapid). Relative density change was calculated at year 1, 2, and 5 during follow-up in relation to treatments and CYP2D6 activity.
Mean relative DA decreased under the follow-up period, with a more pronounced MD reduction in premenopausal patients. No significant effect of chemotherapy, aromatase inhibitors, goserelin, or CYP2D6 activity on DA change was found. DA did not revert to baseline levels after tamoxifen discontinuation.
Our results indicate that other systemic adjuvant therapy does not further reduce MD in tamoxifen-treated breast cancer patients. We could not confirm the previously suggested association between CYP2D6 activity and MD reduction in a clinical setting with multimodality adjuvant treatment. No rebound effect on MD decline after tamoxifen discontinuation was evident.
乳腺密度的变化已被认为是他莫昔芬反应的替代指标。我们研究了额外的辅助全身治疗和 CYP2D6 活性对接受他莫昔芬治疗的绝经前和绝经后乳腺癌患者队列中 MD 变化的影响。
纳入 2006-2014 年瑞典乳腺癌患者(n=699),进行 CYP2D6 基因分型,术后至少接受 3 个月他莫昔芬治疗,基线时至少有一次随访数字乳房 X 线摄影,并至少有一次随访数字乳房 X 线摄影。其他辅助全身治疗包括化疗、戈舍瑞林和芳香化酶抑制剂。使用自动 STRATUS 方法评估 MD(致密区域)的变化。根据基线特征、治疗和 CYP2D6 活性(差、中间、广泛和超快)对患者进行分层。在随访期间的第 1、2 和 5 年计算相对密度变化与治疗和 CYP2D6 活性的关系。
平均相对 DA 在随访期间下降,绝经前患者的 MD 降低更为明显。未发现化疗、芳香化酶抑制剂、戈舍瑞林或 CYP2D6 活性对 DA 变化有显著影响。停用他莫昔芬后,DA 未恢复到基线水平。
我们的结果表明,其他辅助全身治疗并不能进一步降低接受他莫昔芬治疗的乳腺癌患者的 MD。我们无法在多模式辅助治疗的临床环境中证实先前提出的 CYP2D6 活性与 MD 减少之间的关联。在停用他莫昔芬后,MD 下降没有明显的反弹效应。