Literature DB >> 31367551

Whole-tumor perfusion CT using texture analysis in unresectable stage IIIA/B non-small cell lung cancer treated with recombinant human endostatin.

Lei Shi1,2,3, Xiang-Lan Zhou2, Jing-Jing Sun2, Jie-Hui Huang2, Xu Wang2, Kai Li2, Pei-Pei Pang4, Yu-Jin Xu5,6, Ming Chen5,6, Min-Ming Zhang1.   

Abstract

BACKGROUND: To observe the dynamic changes of blood perfusion with whole-tumor computed tomography (CT) perfusion imaging using texture analysis in patients with unresectable stage IIIA/B non-small cell lung cancer (NSCLC) treated with recombinant human endostatin (Endostar).
METHODS: This phase II clinical trial recruited 11 patients diagnosed with stage IIIA/B NSCLC. Histological examination prior to treatment revealed squamous cell carcinoma in 4 cases and adenocarcinoma in 7 cases. All patients underwent contrast-enhanced perfusion CT at baseline and a second CT scan 1 week after treatment initiation with Endostar. CT perfusion images including blood flow (BF), blood volume (BV), and permeability (PMB) were imported into OmniKinetics software to quantitatively assess the texture features. Skewness, kurtosis, and entropy were calculated at baseline and after anti-angiogenic therapy. Changes in tumor were analyzed using Wilcoxon signed-rank test. The association of parameters with survival was evaluated using Cox proportional hazards regression model.
RESULTS: There were no statistical differences in the mean values of BF, BV, and PMB before and after treatment (P=0.594, 0.477 and 0.328, respectively). The skewness on BF images demonstrated significant differences at baseline and after treatment (0.6±2.7 vs. 1.0±2.6, P=0.010), while skewness of BV and PMB showed no significant variation (P=0.477 and 0.213, respectively). The kurtosis and entropy for BF, BV and PMB showed no significant differences (all P>0.05). In adenocarcinoma, the mean BF showed no significant differences at baseline and after treatment (76.5±25.7 vs. 101.2±46.4, P=0.398), while skewness for BF was significantly higher after treatment than at baseline (-0.19±3.3 vs. 0.59±3.2, P=0.028). No significant associations were found between perfusion CT imaging parameters and progression-free survival.
CONCLUSIONS: These results suggested that blood perfusion showed improvement with whole-tumor perfusion CT using texture analysis in patients with stage IIIA/B NSCLC treated by Endostar.

Entities:  

Keywords:  CT perfusion imaging; non-small cell lung cancer (NSCLC); recombinant human endostatin (rhES); texture analysis

Year:  2019        PMID: 31367551      PMCID: PMC6629568          DOI: 10.21037/qims.2019.06.05

Source DB:  PubMed          Journal:  Quant Imaging Med Surg        ISSN: 2223-4306


  24 in total

Review 1.  American Society of Clinical Oncology treatment of unresectable non-small-cell lung cancer guideline: update 2003.

Authors:  David G Pfister; David H Johnson; Christopher G Azzoli; William Sause; Thomas J Smith; Sherman Baker; Jemi Olak; Diane Stover; John R Strawn; Andrew T Turrisi; Mark R Somerfield
Journal:  J Clin Oncol       Date:  2003-12-22       Impact factor: 44.544

Review 2.  Antiangiogenesis in cancer therapy--endostatin and its mechanisms of action.

Authors:  Judah Folkman
Journal:  Exp Cell Res       Date:  2005-12-22       Impact factor: 3.905

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Journal:  Lung Cancer       Date:  2009-09-24       Impact factor: 5.705

8.  Concurrent versus sequential chemoradiotherapy with cisplatin and vinorelbine in locally advanced non-small cell lung cancer: a randomized study.

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Journal:  Lung Cancer       Date:  2004-10       Impact factor: 5.705

9.  Endostar, a novel recombinant human endostatin, exerts antiangiogenic effect via blocking VEGF-induced tyrosine phosphorylation of KDR/Flk-1 of endothelial cells.

Authors:  Yun Ling; Yong Yang; Na Lu; Qi-dong You; Sen Wang; Ying Gao; Yan Chen; Qing-Long Guo
Journal:  Biochem Biophys Res Commun       Date:  2007-07-10       Impact factor: 3.575

10.  Perfusion CT in patients with advanced bronchial carcinomas: a novel chance for characterization and treatment monitoring?

Authors:  F Kiessling; J Boese; C Corvinus; J R Ederle; I Zuna; S O Schoenberg; G Brix; A Schmähl; S Tuengerthal; F Herth; H U Kauczor; M Essig
Journal:  Eur Radiol       Date:  2004-03-17       Impact factor: 5.315

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