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氟脱氧葡萄糖正电子发射断层扫描(FDG PET-CT)上的代谢肿瘤和淋巴结对新辅助化疗的反应可预测食管腺癌患者的病理反应和生存。

Metabolic tumour and nodal response to neoadjuvant chemotherapy on FDG PET-CT as a predictor of pathological response and survival in patients with oesophageal adenocarcinoma.

机构信息

Department of Upper Gastrointestinal and General Surgery, Guy's & St Thomas' Hospital, East Wing Link Corridor, London, SE1 7EH, UK.

School of Cancer and Pharmaceutical Sciences, King's College London, London, UK.

出版信息

Eur Radiol. 2023 May;33(5):3647-3659. doi: 10.1007/s00330-023-09482-7. Epub 2023 Mar 15.

Abstract

OBJECTIVES

2-deoxy-2[F]Fluoro-D-glucose (FDG) PET-CT has an emerging role in assessing response to neoadjuvant therapy in oesophageal cancer. This study evaluated FDG PET-CT in predicting pathological tumour response (pTR), pathological nodal response (pNR) and survival.

METHODS

Cohort study of 75 patients with oesophageal or oesophago-gastric junction (GOJ) adenocarcinoma treated with neoadjuvant chemotherapy then surgery at Guy's and St Thomas' NHS Foundation Trust, London (2017-2020). Standardised uptake value (SUV) metrics on pre- and post-treatment FDG PET-CT in the primary tumour (mTR) and loco-regional lymph nodes (mNR) were derived. Optimum SUV thresholds for predicting pathological response were identified using receiver operating characteristic analysis. Predictive accuracy was compared to PERCIST (30% SUV reduction) and MUNICON (35%) criteria. Survival was assessed using Cox regression.

RESULTS

Optimum tumour SUV decrease for predicting pTR was 51.2%. A 50% cut-off predicted pTR with 73.5% sensitivity, 69.2% specificity and greater accuracy than PERCIST or MUNICON (area under the curve [AUC] 0.714, PERCIST 0.631, MUNICON 0.659). Using a 30% SUV threshold, mNR predicted pNR with high sensitivity but low specificity (AUC 0.749, sensitivity 92.6%, specificity 57.1%, p = 0.010). pTR, mTR, pNR and mNR were independent predictive factors for survival (pTR hazard ratio [HR] 0.10 95% confidence interval [CI] 0.03-0.34; mTR HR 0.17 95% CI 0.06-0.48; pNR HR 0.17 95% CI 0.06-0.54; mNR HR 0.13 95% CI 0.02-0.66).

CONCLUSIONS

Metabolic tumour and nodal response predicted pTR and pNR, respectively, in patients with oesophageal or GOJ adenocarcinoma. However, currently utilised response criteria may not be optimal. pTR, mTR, pNR and mNR were independent predictors of survival.

KEY POINTS

• FDG PET-CT has an emerging role in evaluating response to neoadjuvant therapy in patients with oesophageal cancer. • Prospective cohort study demonstrated that metabolic response in the primary tumour and lymph nodes was predictive of pathological response in a cohort of patients with adenocarcinoma of the oesophagus or oesophago-gastric junction treated with neoadjuvant chemotherapy followed by surgical resection. • Patients who demonstrated a response to neoadjuvant chemotherapy in the primary tumour or lymph nodes on FDG PET-CT demonstrated better survival and reduced rates of tumour recurrence.

摘要

目的

2-脱氧-2[F]氟-D-葡萄糖(FDG)PET-CT 在评估食管癌新辅助治疗反应方面具有新兴作用。本研究评估了 FDG PET-CT 在预测病理肿瘤反应(pTR)、病理淋巴结反应(pNR)和生存方面的作用。

方法

这是一项在伦敦盖伊和圣托马斯国民保健信托基金会(Guy's and St Thomas' NHS Foundation Trust)进行的 75 例食管或食管胃交界(GOJ)腺癌患者的队列研究,这些患者接受了新辅助化疗,然后进行了手术(2017-2020 年)。在原发肿瘤(mTR)和局部淋巴结(mNR)的 FDG PET-CT 上获得治疗前后的标准化摄取值(SUV)指标。使用受试者工作特征分析确定预测病理反应的最佳 SUV 阈值。与 PERCIST(SUV 降低 30%)和 MUNICON(SUV 降低 35%)标准相比,比较了预测准确性。使用 Cox 回归评估生存情况。

结果

预测 pTR 的最佳肿瘤 SUV 下降为 51.2%。使用 50%的截断值预测 pTR 的灵敏度为 73.5%,特异性为 69.2%,准确性优于 PERCIST 或 MUNICON(曲线下面积[AUC]0.714,PERCIST 0.631,MUNICON 0.659)。使用 30%的 SUV 阈值,mNR 预测 pNR 的敏感性高,但特异性低(AUC 0.749,灵敏度 92.6%,特异性 57.1%,p=0.010)。pTR、mTR、pNR 和 mNR 是生存的独立预测因素(pTR 风险比[HR]0.10,95%置信区间[CI]0.03-0.34;mTR HR 0.17,95% CI 0.06-0.48;pNR HR 0.17,95% CI 0.06-0.54;mNR HR 0.13,95% CI 0.02-0.66)。

结论

在患有食管或 GOJ 腺癌的患者中,代谢肿瘤和淋巴结反应分别预测了 pTR 和 pNR。然而,目前使用的反应标准可能并不理想。pTR、mTR、pNR 和 mNR 是生存的独立预测因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6076/10121512/6b53d41cd60a/330_2023_9482_Fig1_HTML.jpg

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