卵巢癌磁化转移成像:与组织细胞性和新辅助化疗后变化相关的初步经验。

BJR open Pub Date : 2022-05-02 eCollection Date: 2022-01-01 DOI:10.1259/bjro.20210078
Surrin S Deen, Mary A McLean, Andrew B Gill, Robin A F Crawford, John Latimer, Peter Baldwin, Helena M Earl, Christine A Parkinson, Sarah Smith, Charlotte Hodgkin, Mercedes Jimenez-Linan, Cara R Brodie, Ilse Patterson, Helen C Addley, Susan J Freeman, Penelope M Moyle, Martin J Graves, Evis Sala, James D Brenton, Ferdia A Gallagher
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引用次数: 0

摘要

研究目的研究高等级浆液性卵巢癌(HGSOC)中磁化传递(MT)成像与组织大分子之间的关系,以及新辅助化疗(NACT)后MT比值(MTR)是否发生变化:这是一项前瞻性观察研究。方法:这是一项前瞻性观察研究。将MTR与组织学和免疫组化的量化结果进行比较。对于部分患者(n = 5),在 NACT 后再次进行 MT 成像。采用 Shapiro-Wilk 检验评估数据的正态性,然后采用 Spearman 秩检验或 Pearson 相关检验比较 MTR 与组织量化结果。Wilcoxon 符号秩检验用于评估治疗后 MTR 的变化:结果:治疗前肿瘤的 MTR 为 21.9 ± 3.1%(平均值 ± S.D.)。MTR与细胞度呈正相关,rho = 0.56(p < 0.05),与肿瘤体积呈负相关,ρ = -0.72(p = 0.01)。MTR 与细胞外蛋白、胶原蛋白 IV 或层粘蛋白没有相关性(p = 0.40 和 p = 0.90)。在 NACT 前后成像的患者中,每个病例的 MTR 都有所增加,治疗前平均 MTR 为 20.6 ± 3.1%(中位数 21.1),治疗后平均 MTR 为 25.6 ± 3.4%(中位数 26.5)(p = 0.06):在治疗无效的HGSOC中,MTR与细胞性相关,可能反映了细胞内大分子的浓度。MT也可检测HGSOC对NACT的反应,但需要更大规模的研究来验证这一发现:HGSOC中的MTR受细胞性的影响。这可用于评估治疗后细胞的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Magnetization transfer imaging of ovarian cancer: initial experiences of correlation with tissue cellularity and changes following neoadjuvant chemotherapy.

Magnetization transfer imaging of ovarian cancer: initial experiences of correlation with tissue cellularity and changes following neoadjuvant chemotherapy.

Magnetization transfer imaging of ovarian cancer: initial experiences of correlation with tissue cellularity and changes following neoadjuvant chemotherapy.

Magnetization transfer imaging of ovarian cancer: initial experiences of correlation with tissue cellularity and changes following neoadjuvant chemotherapy.

Objectives: To investigate the relationship between magnetization transfer (MT) imaging and tissue macromolecules in high-grade serous ovarian cancer (HGSOC) and whether MT ratio (MTR) changes following neoadjuvant chemotherapy (NACT).

Methods: This was a prospective observational study. 12 HGSOC patients were imaged before treatment. MTR was compared to quantified tissue histology and immunohistochemistry. For a subset of patients (n = 5), MT imaging was repeated after NACT. The Shapiro-Wilk test was used to assess for normality of data and Spearman's rank-order or Pearson's correlation tests were then used to compare MTR with tissue quantifications. The Wilcoxon signed-rank test was used to assess for changes in MTR after treatment.

Results: Treatment-naïve tumour MTR was 21.9 ± 3.1% (mean ± S.D.). MTR had a positive correlation with cellularity, rho = 0.56 (p < 0.05) and a negative correlation with tumour volume, ρ = -0.72 (p = 0.01). MTR did not correlate with the extracellular proteins, collagen IV or laminin (p = 0.40 and p = 0.90). For those patients imaged before and after NACT, an increase in MTR was observed in each case with mean MTR 20.6 ± 3.1% (median 21.1) pre-treatment and 25.6 ± 3.4% (median 26.5) post-treatment (p = 0.06).

Conclusion: In treatment-naïve HGSOC, MTR is associated with cellularity, possibly reflecting intracellular macromolecular concentration. MT may also detect the HGSOC response to NACT, however larger studies are required to validate this finding.

Advances in knowledge: MTR in HGSOC is influenced by cellularity. This may be applied to assess for cell changes following treatment.

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