Application of cellular microstructural diffusion MRI (cell size imaging) in rectal lesions: a preliminary study.

IF 3.5 3区 医学 Q2 ONCOLOGY Frontiers in Oncology Pub Date : 2025-02-03 eCollection Date: 2025-01-01 DOI:10.3389/fonc.2025.1535271
Peisi Kou, Liangjie Lin, Ying Li, Hui Qin, Kun Zhang, Wenhua Zhang, Juan Li, Yong Zhang, Jingliang Cheng
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Parameters including mean cell diameter (d<sub>mean</sub>), intracellular fraction (v<sub>in</sub>), extracellular diffusivity (d<sub>ex</sub>), cellularity, and apparent diffusion coefficient (ADC) values (ADC<sub>PGSE</sub>, ADC<sub>17Hz</sub>, ADC<sub>33Hz</sub>, and ADC of conventional DWI) were measured in different histopathologic types, grades, stages, and structure invasion statuses. The receiver operating characteristic (ROC) curve analysis was used to evaluate diagnostic power. The sensitivity, specificity, and the corresponding area under the curves (AUCs) were calculated.</p><p><strong>Results: </strong>Our preliminary results illustrated that malignant lesion showed higher v<sub>in</sub> and cellularity ([0.2867 ± 0.0697] vs. [0.1856 ± 0.1011], [2.3508 ± 0.6055] vs. [1.2716 ± 0.4574], all <i>P</i><0.05), lower d<sub>ex</sub> and ADC values (ADC<sub>PGSE</sub>, ADC<sub>17Hz</sub>, and ADC of conventional DWI) compared to benign lesion ([2.1637 ± 0.3303 μm<sup>2</sup>/ms] vs. [2.5595 ± 0.5085 μm<sup>2</sup>/ms], [0.9238 (0.7959, 1.0741) ×10<sup>-3</sup> mm<sup>2</sup>/s] vs. [1.3373 ± 0.3902×10<sup>-3</sup> mm<sup>2</sup>/s], [1.3204 ± 0.2342×10<sup>-3</sup> mm<sup>2</sup>/s] vs. [1.8029 ± 0.3119×10<sup>-3</sup> mm<sup>2</sup>/s], [0.7400 (0.6750, 0.8375) ×10<sup>-3</sup> mm<sup>2</sup>/s] vs. [1.0550 ± 1.1191×10<sup>-3</sup> mm<sup>2</sup>/s], all <i>P</i><0.05), while no significant difference was seen for d<sub>mean</sub>. V<sub>in</sub> and cellularity of rectal common adenocarcinoma (AC) were significantly higher than those of rectal mucinous adenocarcinoma (MC) ([0.2994 ± 0.0626] vs. [0.2028 ± 0.0571], [2.4579 ± 0.5553] vs. [1.6412 ± 0.4347], all <i>P</i><0.05), while dex and ADC values (ADC<sub>PGSE</sub>, ADC<sub>17Hz</sub>, ADC<sub>33Hz</sub>, and ADC of conventional DWI) were lower in AC ([2.1189 ± 0.3187 μm<sup>2</sup>/ms] vs. [2.4609 ± 0.2534 μm<sup>2</sup>/ms], [0.8996 ± 0.1583×10<sup>-3</sup> mm<sup>2</sup>/s] vs. [1.2072 ± 0.2326×10<sup>-3</sup> mm<sup>2</sup>/s], [1.2714 ± 0.1916×10<sup>-3</sup> mm<sup>2</sup>/s] vs. [1.6451 ± 0.2420×10<sup>-3</sup> mm<sup>2</sup>/s], [1.8963 (1.6481, 2.1138) ×10<sup>-3</sup> mm<sup>2</sup>/s] vs. [2.3104 ± 0.3851×10<sup>-3</sup> mm<sup>2</sup>/s], [0.7341 ± 0.8872×10<sup>-3</sup> mm<sup>2</sup>/s] vs. [1.1410 ± 0.1840×10<sup>-3</sup> mm<sup>2</sup>/s], all <i>P</i><0.05). In AC group, the d<sub>mean</sub> had significant difference between negative and positive tumor budding (TB) ([13.2590 ± 1.3255 μm] vs. [14.3014 ± 1.1830 μm], <i>P</i><0.05). No significant difference of d<sub>mean</sub>, v<sub>in</sub>, d<sub>ex</sub>, cellularity or ADC values was observed in AC with different grade, T stage, N stage, perineural and lymphovascular invasion (all <i>P</i>>0.05). The ROC curves showed that the area under the curves (AUCs) of v<sub>in</sub>, d<sub>ex</sub>, cellularity, and ADC values (ADC<sub>PGSE</sub>, ADC<sub>17Hz</sub>, and ADC of conventional DWI) for distinguishing malignant and benign lesion were 0.803, 0.757, 0.948, 0.807, 0.908 and 0.905, respectively. The AUCs of v<sub>in</sub>, d<sub>ex</sub>, cellularity, and ADC values (ADC<sub>PGSE</sub>, ADC<sub>17Hz</sub>, ADC<sub>33Hz</sub>, and ADC of conventional DWI) in distinguishing AC from MC were 0.887, 0.802, 0.906, 0.896, 0.896, 0.781 and 0.991, respectively. The AUC of the d<sub>mean</sub> for evaluating TB status was 0.726. The AUC of ADC from conventional DWI for evaluating WHO grade was 0.739.</p><p><strong>Conclusion: </strong>Cellular microstructural mapping by the IMPULSED method has great potential in preoperative evaluation of rectal lesions. It could be helpful in differentiating malignant and benign lesions, distinguishing AC from MC, and in predicting the TB status.</p>","PeriodicalId":12482,"journal":{"name":"Frontiers in Oncology","volume":"15 ","pages":"1535271"},"PeriodicalIF":3.5000,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11830574/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fonc.2025.1535271","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
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Abstract

Objectives: To explore the value of cellular microstructural mapping by IMPULSED (imaging microstructural parameters using limited spectrally edited diffusion) method in evaluating the histological type and prognostic factors of rectal lesions.

Materials and methods: Sixty-six patients with rectal lesions were enrolled in this study. All subjects underwent MRI scans including conventional diffusion weighted imaging (DWI) and the IMPULSED MRI scans of oscillating gradient spin-echo (OGSE) and pulse gradient spin-echo (PGSE) sequences. Parameters including mean cell diameter (dmean), intracellular fraction (vin), extracellular diffusivity (dex), cellularity, and apparent diffusion coefficient (ADC) values (ADCPGSE, ADC17Hz, ADC33Hz, and ADC of conventional DWI) were measured in different histopathologic types, grades, stages, and structure invasion statuses. The receiver operating characteristic (ROC) curve analysis was used to evaluate diagnostic power. The sensitivity, specificity, and the corresponding area under the curves (AUCs) were calculated.

Results: Our preliminary results illustrated that malignant lesion showed higher vin and cellularity ([0.2867 ± 0.0697] vs. [0.1856 ± 0.1011], [2.3508 ± 0.6055] vs. [1.2716 ± 0.4574], all P<0.05), lower dex and ADC values (ADCPGSE, ADC17Hz, and ADC of conventional DWI) compared to benign lesion ([2.1637 ± 0.3303 μm2/ms] vs. [2.5595 ± 0.5085 μm2/ms], [0.9238 (0.7959, 1.0741) ×10-3 mm2/s] vs. [1.3373 ± 0.3902×10-3 mm2/s], [1.3204 ± 0.2342×10-3 mm2/s] vs. [1.8029 ± 0.3119×10-3 mm2/s], [0.7400 (0.6750, 0.8375) ×10-3 mm2/s] vs. [1.0550 ± 1.1191×10-3 mm2/s], all P<0.05), while no significant difference was seen for dmean. Vin and cellularity of rectal common adenocarcinoma (AC) were significantly higher than those of rectal mucinous adenocarcinoma (MC) ([0.2994 ± 0.0626] vs. [0.2028 ± 0.0571], [2.4579 ± 0.5553] vs. [1.6412 ± 0.4347], all P<0.05), while dex and ADC values (ADCPGSE, ADC17Hz, ADC33Hz, and ADC of conventional DWI) were lower in AC ([2.1189 ± 0.3187 μm2/ms] vs. [2.4609 ± 0.2534 μm2/ms], [0.8996 ± 0.1583×10-3 mm2/s] vs. [1.2072 ± 0.2326×10-3 mm2/s], [1.2714 ± 0.1916×10-3 mm2/s] vs. [1.6451 ± 0.2420×10-3 mm2/s], [1.8963 (1.6481, 2.1138) ×10-3 mm2/s] vs. [2.3104 ± 0.3851×10-3 mm2/s], [0.7341 ± 0.8872×10-3 mm2/s] vs. [1.1410 ± 0.1840×10-3 mm2/s], all P<0.05). In AC group, the dmean had significant difference between negative and positive tumor budding (TB) ([13.2590 ± 1.3255 μm] vs. [14.3014 ± 1.1830 μm], P<0.05). No significant difference of dmean, vin, dex, cellularity or ADC values was observed in AC with different grade, T stage, N stage, perineural and lymphovascular invasion (all P>0.05). The ROC curves showed that the area under the curves (AUCs) of vin, dex, cellularity, and ADC values (ADCPGSE, ADC17Hz, and ADC of conventional DWI) for distinguishing malignant and benign lesion were 0.803, 0.757, 0.948, 0.807, 0.908 and 0.905, respectively. The AUCs of vin, dex, cellularity, and ADC values (ADCPGSE, ADC17Hz, ADC33Hz, and ADC of conventional DWI) in distinguishing AC from MC were 0.887, 0.802, 0.906, 0.896, 0.896, 0.781 and 0.991, respectively. The AUC of the dmean for evaluating TB status was 0.726. The AUC of ADC from conventional DWI for evaluating WHO grade was 0.739.

Conclusion: Cellular microstructural mapping by the IMPULSED method has great potential in preoperative evaluation of rectal lesions. It could be helpful in differentiating malignant and benign lesions, distinguishing AC from MC, and in predicting the TB status.

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细胞微结构扩散MRI(细胞大小成像)在直肠病变中的应用:初步研究。
目的:探讨脉冲(脉冲成像显微结构参数利用有限的光谱编辑扩散)方法在评估直肠病变的组织学类型和预后因素中的价值。材料和方法:本研究纳入66例直肠病变患者。所有受试者均接受MRI扫描,包括常规弥散加权成像(DWI)和脉冲梯度自旋回波(OGSE)和脉冲梯度自旋回波(PGSE)序列的脉冲MRI扫描。测量不同组织病理类型、分级、分期和结构侵袭状态下的平均细胞直径(dmean)、细胞内分数(vin)、细胞外扩散率(dex)、细胞度和表观扩散系数(ADC)值(ADCPGSE、ADC17Hz、ADC33Hz和常规DWI ADC)。采用受试者工作特征(ROC)曲线分析评价诊断效能。计算灵敏度、特异度及相应的曲线下面积(auc)。结果:我们的初步结果显示,恶性病变的vin和细胞度([0.2867±0.0697]比[0.1856±0.1011],[2.3508±0.6055]比[1.2716±0.4574],所有Pex和ADC值(ADCPGSE, ADC17Hz, ADC)均高于良性病变([2.1637±0.3303 μm2/ms]比[2.5595±0.5085 μm2/ms], [0.9238 (0.7959, 1.0741) ×10-3 mm2/s]比[1.3373±0.3902×10-3 mm2/s],[1.3204±0.2342×10-3 mm2/s]比[1.8029±0.3119×10-3 mm2/s], [0.7400 (0.6750,0.8375 (×10-3 mm2/s) vs.[1.0550±1.1191×10-3 mm2/s],均为平均值。直肠普通腺癌(AC)的Vin和细胞数量均显著高于直肠粘液腺癌(MC)([0.2994±0.0626]比[0.2028±0.0571],[2.4579±0.5553]比[1.6412±0.4347],常规DWI的PPGSE、ADC17Hz、ADC33Hz和ADC)均低于AC([2.1189±0.3187 μm2/ms]比[2.4609±0.2534 μm2/ms]、[0.8996±0.1583×10-3 mm2/s]比[1.2072±0.2326×10-3 mm2/s]、[1.2714±0.1916×10-3 mm2/s]比[1.6451±0.2420×10-3 mm2/s]、[1.8963(1.6481、(2.1138) ×10-3 mm2/s vs.[2.3104±0.3851×10-3 mm2/s],[0.7341±0.8872×10-3 mm2/s] vs.[1.1410±0.1840×10-3 mm2/s],肿瘤出芽(TB)阴性与阳性Pmean([13.2590±1.3255 μm] vs.[14.3014±1.1830 μm],不同分级、T期、N期、周围神经及淋巴血管侵犯AC的Pmean、vin、dex、细胞度或ADC值均有显著性差异(P < 0.05)。ROC曲线显示,vin、指数、细胞度和ADC值(ADCPGSE、ADC17Hz和常规DWI ADC)区分良恶性病变的曲线下面积(auc)分别为0.803、0.757、0.948、0.807、0.908和0.905。vin、指数、细胞度和ADC值(ADCPGSE、ADC17Hz、ADC33Hz和常规DWI ADC)区分AC和MC的auc分别为0.887、0.802、0.906、0.896、0.896、0.781和0.991。评价结核状态的均值AUC为0.726。常规DWI ADC评价WHO分级的AUC为0.739。结论:脉冲细胞显微结构定位在直肠病变的术前评估中具有很大的应用潜力。它可以帮助鉴别恶性和良性病变,区分AC和MC,并预测结核状态。
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来源期刊
Frontiers in Oncology
Frontiers in Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
6.20
自引率
10.60%
发文量
6641
审稿时长
14 weeks
期刊介绍: Cancer Imaging and Diagnosis is dedicated to the publication of results from clinical and research studies applied to cancer diagnosis and treatment. The section aims to publish studies from the entire field of cancer imaging: results from routine use of clinical imaging in both radiology and nuclear medicine, results from clinical trials, experimental molecular imaging in humans and small animals, research on new contrast agents in CT, MRI, ultrasound, publication of new technical applications and processing algorithms to improve the standardization of quantitative imaging and image guided interventions for the diagnosis and treatment of cancer.
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