Association between 21-gene-assay and detection of disseminated tumor cells in patients with early breast cancer: results from the IRMA trial

被引:0
作者
Volmer, Lea L. [1 ]
Dannehl, Dominik [1 ]
Engler, Tobias [1 ]
Hahn, Markus [1 ]
Walter, Christina B. [1 ]
Wallwiener, Markus [2 ]
Brucker, Sara Y. [1 ]
Taran, Florin-Andrei [3 ]
Hartkopf, Andreas D. [1 ,4 ]
机构
[1] Univ Med Ctr Tubingen, Dept Womens Hlth, D-72076 Tubingen, Germany
[2] Univ Med Ctr Heidelberg, Dept Gynecol & Obstet, D-69120 Heidelberg, Germany
[3] Freiburg Univ, Dept Gynecol & Obstet, D-79085 Freiburg, Germany
[4] Ulm Univ, Dept Gynecol & Obstet, D-89081 Ulm, Germany
关键词
Disseminated tumor cells; Oncotype DX; Minimal residual disease; Breast cancer; Individualized therapy; BONE-MARROW; TREATMENT DECISIONS; ONCOTYPE DX(R); RECURRENCE; ASSAY; RISK;
D O I
10.1007/s10549-023-07031-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeDisseminated tumor cells (DTCs) in the bone marrow (BM) are known to be of prognostic value for patients with early breast cancer (EBC). In addition to histopathological features, multigene expression assays, such as the commercially available 21-gene Breast Recurrence Score & REG; assay, have been validated for evaluating prognosis and making decisions concerning adjuvant treatment in EBC. In a previous retrospective study from our group, the 21-gene assay was shown to be associated with DTC-detection. A secondary endpoint of the prospective IRMA trial was to evaluate the association between Recurrence Score & REG; (RS) result and tumor cell dissemination in patients with EBC.MethodsDTC-status and RS result were assessed in patients with ER-positive/HER2-negative EBC with 0-3 pathologic lymph nodes who underwent primary surgical treatment at the Department for Women's Health of Tuebingen University, Germany.ResultsPatients with a high RS result (& GE; 26) were more frequently DTC-positive (22.6%) than patients with a low RS result (8.6%, p = 0.034). The odds for DTC-positivity increased with rising RS values (p = 0.047).ConclusionWe therefore confirm that a high genomic risk is associated with tumor cell dissemination into the BM. Further trials are needed to investigate whether therapeutic decisions could be further individualized by combining DTC-status and prognostic gene signature testing.
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收藏
页码:67 / 72
页数:6
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