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患者和疾病因素在早期可手术乳腺癌辅助全身治疗决策中的作用:ASCO 更新对加拿大安大略癌症护理指南的认可。

Role of Patient and Disease Factors in Adjuvant Systemic Therapy Decision Making for Early-Stage, Operable Breast Cancer: Update of the ASCO Endorsement of the Cancer Care Ontario Guideline.

机构信息

1University of Utah Huntsman Cancer Institute, Salt Lake City, UT.

2American Society of Clinical Oncology, Alexandria, VA.

出版信息

J Clin Oncol. 2019 Aug 1;37(22):1965-1977. doi: 10.1200/JCO.19.00948. Epub 2019 Jun 17.

Abstract

PURPOSE

To update the American Society of Clinical Oncology endorsement of the Cancer Care Ontario recommendations on the Role of Patient and Disease Factors in Adjuvant Systemic Therapy Decision Making for Early-Stage, Operable Breast Cancer.

METHODS

Two phase III trials-the Trial Assigning Individualized Options for Treatment (TAILORx) in women with hormone receptor-positive, node-negative tumors and the Microarray in Node-Negative and 1 to 3 Positive Lymph Node Disease May Avoid Chemotherapy (MINDACT) trial-provided the evidence for this update.

UPDATED RECOMMENDATIONS

Shared decision making between clinicians and patients is appropriate for adjuvant systemic therapy for breast cancer. For patients older than age 50 years and whose tumors have Onco DX recurrence scores less than 26, and for patients age 50 years or younger whose tumors have Onco DX recurrence scores less than 16, there is little to no benefit from chemotherapy. Clinicians may offer endocrine therapy alone for these patients. For patients age 50 years or younger with recurrence scores of 16 to 25, clinicians may offer chemoendocrine therapy. Patients with recurrence scores greater than 30 should be considered candidates for chemoendocrine therapy. Based on informal consensus, the Panel recommends that oncologists may offer chemoendocrine therapy to patients with Onco DX scores of 26 to 30.The MammaPrint assay could be used to guide decisions on withholding adjuvant systemic chemotherapy in patients with hormone receptor-positive lymph node-negative breast cancer and in select patients with lymph node-positive cancers. In both patients with node-positive and node-negative disease, evidence of clinical utility of the MammaPrint assay was only apparent in those determined to be at high clinical risk; the Panel thus did not recommend use of MammaPrint assay in patients determined to be at low clinical risk. Remaining recommendations from the 2016 ASCO guideline endorsement are unchanged.Additional information is available at www.asco.org/breast-cancer-guidelines.

摘要

目的

更新美国临床肿瘤学会对安大略省癌症护理推荐的认可,该推荐涉及早期可手术乳腺癌辅助全身治疗决策中患者和疾病因素的作用。

方法

两项 III 期试验——激素受体阳性、淋巴结阴性肿瘤患者的个体化治疗选择试验(TAILORx)和淋巴结阴性和 1 至 3 个阳性淋巴结疾病的微阵列可能避免化疗(MINDACT)试验——为本次更新提供了证据。

更新后的建议

临床医生和患者之间的共同决策适用于乳腺癌的辅助全身治疗。对于年龄大于 50 岁且肿瘤 Onco DX 复发评分小于 26 的患者,以及年龄小于等于 50 岁且肿瘤 Onco DX 复发评分小于 16 的患者,化疗几乎没有获益。对于这些患者,临床医生可以单独提供内分泌治疗。对于复发评分在 16 至 25 之间的年龄小于等于 50 岁的患者,临床医生可以提供化疗联合内分泌治疗。复发评分大于 30 的患者应被视为化疗联合内分泌治疗的候选者。基于非正式共识,专家组建议肿瘤医生可以向 Onco DX 评分为 26 至 30 的患者提供化疗联合内分泌治疗。MammaPrint 检测可用于指导激素受体阳性、淋巴结阴性乳腺癌患者和选择性淋巴结阳性癌症患者是否避免辅助全身化疗。在淋巴结阳性和淋巴结阴性的患者中,MammaPrint 检测的临床实用性证据仅在被认为具有高临床风险的患者中显现;因此,专家组不建议在被认为具有低临床风险的患者中使用 MammaPrint 检测。2016 年 ASCO 指南认可的其余建议保持不变。更多信息可在 www.asco.org/breast-cancer-guidelines 上获取。

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