Abstract
Objectives
To determine the extracellular volume (ECV) fraction derived from equilibrium contrast-enhanced CT for predicting pathological complete response (pCR) after neoadjuvant chemoradiotherapy (NCRT) in locally advanced rectal cancer (LARC).
Methods
The ECV fraction before NCRT (ECVpre) and/or ECV after NCRT (ECVpost) of rectal tumors was assessed, and ECVΔ was calculated as ECVpost − ECVpre. The histopathologic tumor regression grading (TRG) was assessed. pCR (TRG 0 grade) was defined as the absence of viable tumor cells in the primary tumor and lymph nodes. Demographic and clinicopathological characteristics and ECV fraction were compared between the pCR and non-pCR groups. A mixed model was constructed by logistic regression. The performance for predicting pCR was assessed with the area under the receiver-operator curve (AUC). The AUCs of the different methods were compared by the method proposed by DeLong et al.
Results
Seventy-five patients were included; 17 achieved pCR, and 58 achieved non-pCR. The ECVpost (17.05 ± 2.36% vs. 29.94 ± 1.20%; p < 0.001) and ECVΔ (− 17.01 ± 3.01% vs. 0.44 ± 1.45%; p < 0.001) values in the pCR group were significantly lower than those in the non-pCR group. The mixed model that combined ECVpost with ECVΔ achieved an AUC of 0.92 (95% confidence interval (CI) = 0.81–0.98), which was higher than that of ECVpost (AUC, 0.91 (95% CI = 0.80–0.97); p = 0.60) or ECVΔ (AUC, 0.90 (95% CI = 0.79–0.97); p = 0.61).
Conclusions
ECVpost and ECVΔ determined by using equilibrium contrast-enhanced CT were useful in distinguishing between pCR and non-pCR patients with LARC who received NCRT.
Key Points
• ECV post and ECV Δ (ECV post − ECV pre ) differed significantly between the non-pCR and pCR groups.
• ECV pre cannot be used to predict the efficacy of neoadjuvant chemoradiotherapy.
• ECV post combined with ECV Δ had the best performance with an AUC of 0.92 for predicting pCR after NCRT in LARC.
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Abbreviations
- AJCC:
-
American Joint Committee on Cancer
- CA 19-9:
-
Carbohydrate antigen 19-9
- CEA:
-
Carcinoma embryonic antigen
- CTV:
-
Clinical target volume
- ECV:
-
Extracellular volume
- GTV:
-
Gross tumor volume
- ICC:
-
Intra-class correlation coefficient
- IMRT:
-
Intensity-modulated radiation therapy
- LARC:
-
Locally advanced rectal cancer
- NCRT:
-
Neoadjuvant chemoradiotherapy
- OS:
-
Overall survival
- pCR:
-
Pathological complete response
- PFS:
-
Progression-free survival
- TME:
-
Total mesorectal excision
- TRG:
-
Tumor regression grading
- UICC:
-
Union for International Cancer Control
- W&W:
-
Watch and wait
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Acknowledgements
The authors thank Hesong Shen and Daihong Liu, who have been a source of encouragement and inspiration. We acknowledge the support of Xiaoyue Zhang from Siemens Healthineers.
Funding
This project was supported by the 2020 SKY Imaging Research Fund of the Chinese International Medical Foundation (Grant No. Z-2014-07-2003-24), the Natural Science Foundation of Chongqing municipality (No. cstc2021jcyj-msxmX0387), Medical Scientific Research Project of Chongqing Municipal Health Commission (No. 2022WSJK027), the Chongqing Medical Research Project of Combination of Science and Medicine (Grant No. 2021MSXM035), and the Chongqing Natural Science Foundation (Grant No. cstc2021jcyj-msxmX0313).
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The scientific guarantor of this publication is Jiuquan Zhang.
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Two of the authors (Xiaoyue Zhang and Jiaxing Wu) are employees of Siemens Healthineers. The remaining authors declare no relationships with any companies whose products or services may be related to the subject matter of the article.
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Daihong Liu from Chongqing University Cancer Hospital kindly provided statistical advice for this manuscript, and he is one of the authors of this study.
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• retrospective
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• performed at one institution
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Luo, Y., Liu, L., Liu, D. et al. Extracellular volume fraction determined by equilibrium contrast-enhanced CT for the prediction of the pathological complete response to neoadjuvant chemoradiotherapy for locally advanced rectal cancer. Eur Radiol 33, 4042–4051 (2023). https://doi.org/10.1007/s00330-022-09307-z
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DOI: https://doi.org/10.1007/s00330-022-09307-z