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化疗放疗后早期弥散加权磁共振成像对头颈部鳞状细胞癌复发或肿瘤进展的预测价值

Predictive Value of Early Post-Treatment Diffusion-Weighted MRI for Recurrence or Tumor Progression of Head and Neck Squamous Cell Carcinoma Treated with Chemo-Radiotherapy.

作者信息

Brenet Esteban, Barbe Coralie, Hoeffel Christine, Dubernard Xavier, Merol Jean-Claude, Fath Léa, Servagi-Vernat Stéphanie, Labrousse Marc

机构信息

Department of Oto-Rhino-Laryngology, Head and Neck Surgery, Robert Debré University Hospital, 51100 Reims, France.

Clinical Research Unit, Robert Debré University Hospital, 51100 Reims, France.

出版信息

Cancers (Basel). 2020 May 14;12(5):1234. doi: 10.3390/cancers12051234.

DOI:10.3390/cancers12051234
PMID:32422975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7281260/
Abstract

AIMS

To investigate the predictive capacity of early post-treatment diffusion-weighted magnetic resonance imaging (MRI) for recurrence or tumor progression in patients with no tumor residue after chemo-radiotherapy (CRT) for head and neck squamous cell carcinoma, and, to assess the predictive capacity of pre-treatment diffusion-weighted MRI for persistent tumor residue post-CRT.

MATERIALS AND METHOD

A single center cohort study was performed in one French hospital. All patients with squamous cell carcinoma receiving CRT (no surgical indication) were included. Two diffusion-weighted MRI were performed: one within 8 days before CRT and one 3 months after completing CRT with determination of median tumor apparent diffusion coefficient (ADC).

MAIN OUTCOME

The primary endpoint was progression-free survival.

RESULTS

59 patients were included prior to CRT and 46 (78.0%) completed CRT. A post-CRT tumor residue was found in 19/46 (41.3%) patients. In univariate analysis, initial ADC was significantly lower in patients with residue post CRT (0.56 ± 0.11 versus 0.79 ± 0.13; < 0.001). When initial ADC was dichotomized at the median, initial ADC lower than 0.7 was significantly more frequent in patients with residue post CRT (73.7% versus 11.1%, < 0.0001). In multivariate analysis, only initial ADC lower than 0.7 was significantly associated with tumor residue (OR = 22.6; IC [4.9-103.6], < 0.0001). Among 26 patients without tumor residue after CRT and followed up until 12 months, 6 (23.1%) presented recurrence or progression. Only univariate analysis was performed due to a small number of events. The only factor significantly associated with disease progression or early recurrence was the delta ADC ( = 0.0009). When ADC variation was dichotomized at the median, patients with ADC variation greater than 0.7 had time of disease-free survival significantly longer than patients with ADC variation lower than 0.7 (377.5 [286-402] days versus 253 [198-370], < 0.0001). Conclusion and relevance: Diffusion-weighted MRI could be a technique that enables differentiation of patients with high potential for early recurrence for whom intensive post-CRT monitoring is mandatory. Prospective studies with more inclusions would be necessary to validate our results.

摘要

目的

探讨头颈部鳞状细胞癌放化疗(CRT)后无肿瘤残留患者早期治疗后扩散加权磁共振成像(MRI)对复发或肿瘤进展的预测能力,并评估治疗前扩散加权MRI对CRT后持续性肿瘤残留的预测能力。

材料与方法

在一家法国医院进行了一项单中心队列研究。纳入所有接受CRT(无手术指征)的鳞状细胞癌患者。进行了两次扩散加权MRI检查:一次在CRT前8天内,另一次在完成CRT后3个月,测定肿瘤表观扩散系数(ADC)中位数。

主要结局

主要终点是无进展生存期。

结果

59例患者在CRT前纳入,46例(78.0%)完成了CRT。19/46例(41.3%)患者发现CRT后有肿瘤残留。单因素分析显示,CRT后有残留的患者初始ADC显著更低(0.56±0.11对0.79±0.13;<0.001)。当初始ADC以中位数进行二分法划分时,CRT后有残留的患者初始ADC低于0.7的情况显著更常见(73.7%对11.1%,<0.0001)。多因素分析显示,只有初始ADC低于0.7与肿瘤残留显著相关(OR=22.6;IC[4.9 - 103.6],<0.0001)。在26例CRT后无肿瘤残留且随访至12个月的患者中,6例(23.1%)出现复发或进展。由于事件数量少,仅进行了单因素分析。与疾病进展或早期复发显著相关的唯一因素是ADC变化量(=0.0009)。当ADC变化量以中位数进行二分法划分时,ADC变化量大于0.7的患者无病生存期显著长于ADC变化量低于0.7的患者(377.5[286 - 402]天对253[198 - 370]天,<0.0001)。结论与相关性:扩散加权MRI可能是一种能够区分早期复发高风险患者的技术,对于这些患者,CRT后强化监测是必要的。需要更多纳入病例的前瞻性研究来验证我们的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebd/7281260/92f7d57763b4/cancers-12-01234-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebd/7281260/71c79ba6f59f/cancers-12-01234-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebd/7281260/7f6db94fd602/cancers-12-01234-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebd/7281260/09ea038ae0b0/cancers-12-01234-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebd/7281260/92f7d57763b4/cancers-12-01234-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebd/7281260/71c79ba6f59f/cancers-12-01234-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebd/7281260/7f6db94fd602/cancers-12-01234-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebd/7281260/09ea038ae0b0/cancers-12-01234-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebd/7281260/92f7d57763b4/cancers-12-01234-g004.jpg

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