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通过循环肿瘤DNA动力学预测转移性胰腺癌对全身治疗的反应

Prediction of response to systemic treatment by kinetics of circulating tumor DNA in metastatic pancreatic cancer.

作者信息

Kirchweger Patrick, Kupferthaler Alexander, Burghofer Jonathan, Webersinke Gerald, Jukic Emina, Schwendinger Simon, Wundsam Helwig, Biebl Matthias, Petzer Andreas, Rumpold Holger

机构信息

Gastrointestinal Cancer Center, Ordensklinikum Linz, Linz, Austria.

Department of Surgery, Ordensklinikum Linz, Linz, Austria.

出版信息

Front Oncol. 2022 Aug 30;12:902177. doi: 10.3389/fonc.2022.902177. eCollection 2022.

Abstract

INTRODUCTION

Pretherapeutic detectable circulating tumor DNA (ctDNA) represents a promising prognostic biomarker for predicting relapse and overall survival in patients with metastatic pancreatic cancer. However, the prognostic value of ctDNA dynamics during treatment has not been studied thus far. We aimed to investigate the correlation between the change of ctDNA levels and response to treatment in patients treated by systemic therapy.

MATERIAL AND METHODS

CtDNA detection using liquid biopsy (droplet digital PCR (ddPCR) utilizing G12/13 and, if negative, Q61 commercial test kits) was prospectively performed on patients with stage IV pancreatic cancer i) prior to initiation of systemic chemotherapy and ii) serially every 2 weeks until restaging. Detection rates, levels of ctDNA, and the course of the relative ctDNA change (ctDNA kinetics) were correlated to treatment response and clinical outcome.

RESULTS

The detection rate at baseline was 64.3% (45/70), and complete serial measurement records were available for 32 ctDNA-positive patients. Reduction of ctDNA levels below 57.9% of its baseline value at week 2 after treatment initiation was significantly predictive of response to treatment (area under the curve (AUC) = 0.918, sensitivity 91.67%, and specificity 100%) and was associated with prolonged overall survival (OS) (5.7 vs. 11.4 months, p = 0.006) and progression-free survival (PFS) (2.5 vs. 7.7 months, p < 0.000) regardless of treatment line. Pretherapeutic ctDNA detection was independently associated with worse OS in patients receiving a first-line regimen (7 vs. 11.3 months, p = 0.046) and regardless of treatment line (11.4 vs. 15.9 months, p = 0.045) as well as worse PFS (3.4 vs. 10.8 months, p = 0.018).

CONCLUSION

The change in magnitude of ctDNA during systemic treatment allows the prediction of treatment response and is associated with both OS and PFS. This finding adds significant clinical potential to the already established prognostic value of ctDNA positivity in metastatic pancreatic cancer.

摘要

引言

治疗前可检测到的循环肿瘤DNA(ctDNA)是预测转移性胰腺癌患者复发和总生存期的一种很有前景的预后生物标志物。然而,迄今为止尚未研究治疗期间ctDNA动态变化的预后价值。我们旨在研究接受全身治疗的患者中ctDNA水平变化与治疗反应之间的相关性。

材料与方法

对IV期胰腺癌患者前瞻性地进行ctDNA检测,采用液体活检(使用G12/13的液滴数字PCR(ddPCR),若为阴性则使用Q61商业检测试剂盒),i)在开始全身化疗前,ii)每2周进行一次连续检测,直至重新分期。检测率、ctDNA水平以及相对ctDNA变化过程(ctDNA动力学)与治疗反应和临床结果相关。

结果

基线时的检测率为64.3%(45/70),32例ctDNA阳性患者有完整的连续测量记录。治疗开始后第2周时ctDNA水平降至其基线值的57.9%以下,显著预测治疗反应(曲线下面积(AUC)=0.918,敏感性91.67%,特异性100%),且与总生存期(OS)延长(5.7个月对11.4个月,p=0.006)和无进展生存期(PFS)延长(2.5个月对7.7个月,p<0.000)相关,与治疗线无关。治疗前ctDNA检测与接受一线治疗方案的患者较差的OS(7个月对11.3个月,p=0.046)、与治疗线无关的较差OS(11.4个月对15.9个月,p=0.045)以及较差的PFS(3.4个月对10.8个月,p=0.018)独立相关。

结论

全身治疗期间ctDNA水平的变化可预测治疗反应,并与OS和PFS均相关。这一发现为已确立的转移性胰腺癌中ctDNA阳性的预后价值增添了显著的临床潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e088/9468369/1906443121bd/fonc-12-902177-g001.jpg

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