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巴西公立医院使用 21 基因检测对早期乳腺癌进行辅助化疗的大量减少。

Substantial Reduction in Adjuvant Chemotherapy With the Use of the 21-Gene Test to Manage Early Breast Cancer in a Public Hospital in Brazil.

机构信息

Hospital Pérola Byington, São Paulo, Brazil.

Santa Casa de Misericórdia de São Paulo, São Paulo, Brazil.

出版信息

JCO Glob Oncol. 2021 Jun;7:1003-1011. doi: 10.1200/GO.20.00609.

Abstract

PURPOSE

We evaluated the impact of 21-gene test results on treatment decisions for patients with early-stage breast cancer treated under the public health care system in Brazil, Sistema Único de Saúde.

METHODS

Eligible patients treated at Hospital Pérola Byington and Santa Casa de Misericórdia de São Paulo in Brazil were required to have the following characteristics: postsurgery with hormone receptor-positive, human epidermal growth factor 2-negative, node-negative and node-positive, and T1/T2 breast cancer and patients with these characteristics were candidates for adjuvant systemic therapy. Treatment recommendations, chemotherapy plus hormonal therapy (CT + HT) or HT alone, were captured before and after 21-gene test results.

RESULTS

From August 2018 to April 2019, 179 women were enrolled. The mean age was 58 years (29-86 years), 135 (76%) were postmenopausal, and 58 (32%) had node-positive breast cancer. Most patients (61%) had a tumor > 2 cm, including 7% with tumors > 4 cm. Using Recurrence Score (RS) result cut points on the basis of the TAILORx trial, 40 (22%) had RS 0-10, 91 (51%) had RS 11-25, and 48 (27%) had RS 26-100. Before 21-gene testing, 162 of 179 (91%) patients were recommended for CT. After testing, 117 of 179 patients (65%) had changes in CT recommendation: 112 (63%) who were initially recommended CT received HT alone and five (3%) who were initially recommended HT alone received CT + HT. After 21-gene testing, 99% of physicians reported strong confidence in their treatment recommendations.

CONCLUSION

The change in clinical practice at these public hospitals was greater than expected: 66% of initial treatment recommendations were changed to omit CT with 21-gene test results. Clinicopathologic features did not correlate well with 21-gene test results and did not adequately identify those most likely to benefit from CT.

摘要

目的

我们评估了 21 基因检测结果对巴西公共医疗保健系统(Sistema Único de Saúde)下接受治疗的早期乳腺癌患者治疗决策的影响。

方法

在巴西佩罗拉·拜永顿医院(Hospital Pérola Byington)和圣十字慈悲圣母医院(Santa Casa de Misericórdia de São Paulo)接受治疗的符合条件的患者需要具有以下特征:手术后激素受体阳性、人表皮生长因子 2 阴性、淋巴结阴性和淋巴结阳性、T1/T2 乳腺癌以及具有这些特征的患者为辅助全身治疗的候选者。在 21 基因检测结果之前和之后,我们捕获了治疗建议,即化疗加激素治疗(CT+HT)或 HT 单独治疗。

结果

从 2018 年 8 月至 2019 年 4 月,共纳入 179 名女性。平均年龄为 58 岁(29-86 岁),135 名(76%)为绝经后患者,58 名(32%)为淋巴结阳性乳腺癌患者。大多数患者(61%)肿瘤>2cm,包括 7%肿瘤>4cm。基于 TAILORx 试验的 Recurrence Score(RS)结果切点,40 名(22%)患者的 RS 为 0-10,91 名(51%)患者的 RS 为 11-25,48 名(27%)患者的 RS 为 26-100。在进行 21 基因检测之前,179 名患者中的 162 名(91%)被建议进行 CT。检测后,179 名患者中有 117 名(65%)改变了 CT 推荐:112 名(63%)最初推荐 CT 的患者接受了 HT 单独治疗,5 名(3%)最初推荐 HT 单独治疗的患者接受了 CT+HT。进行 21 基因检测后,99%的医生对他们的治疗建议表示强烈的信心。

结论

这些公立医院的临床实践变化超出预期:66%的初始治疗建议被改变为省略 CT,而 21 基因检测结果为阴性。临床病理特征与 21 基因检测结果相关性不佳,不能充分识别最有可能从 CT 中获益的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5385/8457870/1654ea17aec1/go-7-go.20.00609-g002.jpg

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