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[18F]-氟代脱氧葡萄糖正电子发射断层扫描/计算机断层扫描评估激素受体阳性 HER2 阴性转移性乳腺癌患者接受细胞周期蛋白依赖性激酶 4/6 抑制剂治疗后的早期代谢反应。

[18F]-Fluorodeoxyglucose Positron Emission Tomography/CT to Assess the Early Metabolic Response in Patients with Hormone Receptor-Positive HER2-Negative Metastasized Breast Cancer Treated with Cyclin-Dependent 4/6 Kinase Inhibitors.

机构信息

Department of Nuclear Medicine, University Hospital Essen, Essen, Germany.

West German Cancer Center (WTZ), Essen, Germany.

出版信息

Oncol Res Treat. 2021;44(7-8):400-407. doi: 10.1159/000516422. Epub 2021 Jun 8.

Abstract

INTRODUCTION

Addition of cyclin-dependent 4/6 kinase (CDK4/6) inhibitors to endocrine therapy is standard of care in the treatment of women with advanced hormone receptor-positive HER2-negative breast cancer. However, the predictive factors for the treatment response to CDK4/6 inhibitor therapy are poorly elucidated. Early changes in the by [18F]-fluorodeoxyglucose positron emission tomography (FDG-PET) uptake of tumors receiving different kinds of therapy have proven to reliably predict treatment outcomes in a variety of malignancies. Therefore, the feasibility of early metabolic response assessment to predict the long-term treatment response to CDK4/6 inhibitor therapy was evaluated in the present study.

METHODS

Eight patients underwent FDG-PET/CT before and after the initiation of CDK4/6 inhibitor therapy (ribociclib, palbociclib or abemcaciclib). CDK4/6 inhibitor therapy was combined with either aromatase inhibition or fulvestrant. The median interval between the treatment start (including baseline PET) and the follow-up PET examination was 14 days. Conventional radiographic staging was performed 3 months after the start of CDK4/6 inhibitor therapy. The percentual changes in molecular tumor volume, SUVpeak, the summed SUVpeak of up to 5 metastases (PERCIST-5), and total lesion glycolysis (TLG) were calculated for each patient.

RESULTS

Three patients showed progressive disease after 3 months of CDK4/6 inhibitor therapy, whereas 5 patients showed disease control (3 stable disease and 2 partial remission). Disease control was maintained in these patients (follow-up range 7-22 months). Patients with disease control had a significantly greater decline in TLG (-55.3 vs. 16.7%; p < 0.05). The same was true for the PERCIST-5 (-21.9 vs. 11.3%, p < 0.05). All patients with progressive TLG showed treatment failure and/or a poor outcome.

CONCLUSION

Elevated TLG on early FDG-PET seems to be associated with long-term treatment failure and a poor outcome in patients undergoing CDK4/6 inhibitor therapy for metastatic breast cancer. Early findings indicate a potential prognostic value of early FDG-PET in this setting and warrant a prospective evaluation.

摘要

简介

在治疗晚期激素受体阳性 HER2 阴性乳腺癌患者时,将细胞周期蛋白依赖性激酶 4/6(CDK4/6)抑制剂添加到内分泌治疗中是标准的治疗方法。然而,对于 CDK4/6 抑制剂治疗反应的预测因素仍未得到充分阐明。在各种恶性肿瘤中,接受不同治疗的肿瘤的 [18F]-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)摄取的早期变化已被证明能够可靠地预测治疗结果。因此,本研究评估了早期代谢反应评估预测 CDK4/6 抑制剂治疗长期治疗反应的可行性。

方法

8 例患者在开始 CDK4/6 抑制剂治疗(ribociclib、palbociclib 或 abemaciclib)前后进行了 FDG-PET/CT 检查。CDK4/6 抑制剂治疗与芳香化酶抑制或氟维司群联合使用。治疗开始(包括基线 PET)和随访 PET 检查之间的中位间隔时间为 14 天。在开始 CDK4/6 抑制剂治疗后 3 个月进行常规放射学分期。为每位患者计算了分子肿瘤体积、SUVpeak、最多 5 个转移部位的 SUVpeak 总和(PERCIST-5)和总病变糖酵解(TLG)的百分比变化。

结果

3 例患者在 CDK4/6 抑制剂治疗 3 个月后出现疾病进展,而 5 例患者出现疾病控制(3 例稳定疾病和 2 例部分缓解)。这些患者的疾病控制得到了维持(随访范围 7-22 个月)。疾病控制患者的 TLG 下降幅度明显更大(-55.3%与 16.7%;p < 0.05)。PERCIST-5 也是如此(-21.9%与 11.3%,p < 0.05)。所有 TLG 进展的患者均出现治疗失败和/或不良结局。

结论

在接受 CDK4/6 抑制剂治疗转移性乳腺癌的患者中,早期 FDG-PET 上升高的 TLG 似乎与长期治疗失败和不良结局相关。早期发现表明早期 FDG-PET 在这种情况下具有潜在的预后价值,需要进行前瞻性评估。

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