Hormone Laboratory, Department of Medical Biochemistry and Pharmacology, Haukeland University Hospital, Bergen, Norway.
Department of Clinical Science, University of Bergen, Norway.
Mol Oncol. 2021 Apr;15(4):957-967. doi: 10.1002/1878-0261.12865. Epub 2020 Dec 14.
Low steady-state levels of active tamoxifen metabolites have been associated with inferior treatment outcomes. In this retrospective analysis of 406 estrogen receptor-positive breast cancer (BC) patients receiving adjuvant tamoxifen as initial treatment, we have associated our previously reported thresholds for the two active metabolites, Z-endoxifen and Z-4-hydroxy-tamoxifen (Z-4OHtam), with treatment outcomes in an independent cohort of BC patients. Among all patients, metabolite levels did not affect survival. However, in the premenopausal subgroup receiving tamoxifen alone (n = 191) we confirmed an inferior BC -specific survival in patients with the previously described serum concentration threshold of Z-4OHtam ≤ 3.26 nm (HR = 2.37, 95% CI = 1.02-5.48, P = 0.039). The 'dose-response' survival trend in patients categorized to ordinal concentration cut-points of Z-4OHtamoxifen (≤ 3.26, 3.27-8.13, > 8.13 nm) was also replicated (P-trend log-rank = 0.048). Z-endoxifen was not associated with outcome. This is the first study to confirm the association between a published active tamoxifen metabolite threshold and BC outcome in an independent patient cohort. Premenopausal patients receiving 5-year of tamoxifen alone may benefit from therapeutic drug monitoring to ensure tamoxifen effectiveness.
低稳态水平的活性他莫昔芬代谢物与较差的治疗结果相关。在这项对 406 例接受辅助他莫昔芬作为初始治疗的雌激素受体阳性乳腺癌 (BC) 患者的回顾性分析中,我们将之前报道的两种活性代谢物 Z-内消旋体和 Z-4-羟基他莫昔芬 (Z-4OHtam) 的阈值与另一组 BC 患者的治疗结果相关联。在所有患者中,代谢物水平并未影响生存。然而,在接受单独他莫昔芬治疗的绝经前亚组 (n=191) 中,我们在先前描述的血清 Z-4OHtam 浓度阈值≤3.26nm 的患者中证实了 BC 特异性生存的下降 (HR=2.37,95%CI=1.02-5.48,P=0.039)。在 Z-4OHtamoxifen 分类浓度截断点 (≤3.26、3.27-8.13、>8.13nm) 的患者中,“剂量反应”生存趋势也得到了复制 (P 趋势对数秩检验=0.048)。Z-内消旋体与结局无关。这是第一项在独立患者队列中证实已发表的活性他莫昔芬代谢物阈值与 BC 结局相关联的研究。接受 5 年他莫昔芬单独治疗的绝经前患者可能受益于治疗药物监测,以确保他莫昔芬的有效性。