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CTRIAL-IE(ICORG)15 - 34:21基因乳腺癌复发评分®检测对爱尔兰雌激素受体阳性、淋巴结阳性早期乳腺癌化疗处方的影响。

CTRIAL-IE (ICORG) 15-34: The impact of the 21 gene breast recurrence score® assay on chemotherapy prescribing in oestrogen receptor positive, lymph node positive early stage breast cancer in Ireland.

作者信息

Mullally W J, Hassan A, Keegan N, O'Leary C, McSorley L, Mahgoub T, O'Reilly S, Walshe J, Kennedy M J, Coate L, O'Connor M, Keane M, Kelly C M, Duffy K, Murphy C G, Milewski M, Molloy S, Egan K, Murphy V, Breathnach O S, Grogan L, Hennessy B T, Morris P G

机构信息

Cancer Clinical Trials and Research Unit, Beaumont RCSI Cancer Centre, Dublin 9, D09 V2N0, Dublin, Ireland.

Department of Medical Oncology, Cork University Hospital, T12 DC4A, Cork, Ireland.

出版信息

Ir J Med Sci. 2025 Apr 11. doi: 10.1007/s11845-025-03922-7.

Abstract

BACKGROUND

The 21-gene Breast Recurrence Score® (Oncotype DX®) assay has improved the selection of patients for chemotherapy in early breast cancer. Internationally, this test is used in lymph node positive disease, but at the time this study was conducted, it was not reimbursed for this indication in Ireland.

AIMS

Determine how access to the Recurrence Score® testing reduces chemotherapy use and quantifies the impact on oncologists' treatment recommendations.

METHODS

Between March and September 2017, 75 patients were enrolled in a prospective study across ten hospitals. Eligible patients had oestrogen/progesterone receptor positive and HER2 negative breast cancer with 1-3 involved lymph nodes. Following informed consent, demographics were collected and questionnaires completed by a consultant medical oncologist before and after the recurrence score testing, which examined expectations of tumour chemosensitivity, strength of chemotherapy recommendation, and planned treatment.

RESULTS

Recurrence Scores® were available on 74/75 patients. Overall, access to this test led to a 27% reduction in the recommendation for chemotherapy from 68 (92%) to 48 (65%) patients. This was most notable in patients with one (46 versus 34 patients) and two (13 versus seven patients) involved lymph nodes representing a 26% and 46% reduction, respectively. The reduction in chemotherapy use was marked in women aged 50-70 years with one lymph node involved (28 versus 18 patients)-a 36% reduction.

CONCLUSION

Consistent with our hypothesis, broader access to the Recurrence Score® led to a reduction in the use of chemotherapy in Ireland and has subsequently become standard of care.

摘要

背景

21基因乳腺癌复发评分(Oncotype DX)检测改善了早期乳腺癌患者化疗的选择。在国际上,该检测用于淋巴结阳性疾病,但在本研究开展时,爱尔兰尚未对该适应症给予报销。

目的

确定复发评分检测的可及性如何减少化疗的使用,并量化其对肿瘤学家治疗建议的影响。

方法

2017年3月至9月期间,在十家医院对75例患者进行了一项前瞻性研究。符合条件的患者患有雌激素/孕激素受体阳性且HER2阴性的乳腺癌,有1至3个受累淋巴结。在获得知情同意后,收集人口统计学数据,并由肿瘤内科顾问医生在复发评分检测前后完成问卷调查,调查内容包括对肿瘤化疗敏感性的期望、化疗推荐强度和计划治疗方案。

结果

75例患者中有74例获得了复发评分。总体而言,该检测的可及性使化疗推荐率从68例(92%)降至48例(65%),降低了27%。这在有一个(46例对34例)和两个(13例对7例)受累淋巴结的患者中最为显著,分别降低了26%和46%。在50至70岁、有一个淋巴结受累的女性中,化疗使用的减少最为明显(28例对18例),降低了36%。

结论

与我们的假设一致,在爱尔兰,更广泛地使用复发评分导致化疗使用减少,该检测随后成为了标准治疗手段。

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