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E-Poster Display

475P - Diffusion kurtosis imaging signature in predicting the chemotherapeutic response of colorectal liver metastases: The result of the FDZL-MRinCLM study

Date

17 Sep 2020

Session

E-Poster Display

Topics

Cytotoxic Therapy

Tumour Site

Colon and Rectal Cancer

Presenters

Wenhua Li

Citation

Annals of Oncology (2020) 31 (suppl_4): S409-S461. 10.1016/annonc/annonc270

Authors

W. Li1, H. Zhang2, Z. Gong1, T. Tong2, W. Guo1

Author affiliations

  • 1 Department Of Medical Oncology, Fudan University Shanghai Cancer Center, 200032 - Shanghai/CN
  • 2 Department Of Radiology, Fudan University Shanghai Cancer Center, 200032 - Shanghai/CN

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Abstract 475P

Background

The purpose of the FDZL-MRinCLM study (NCT03088163) is to evaluate the feasibility of early parameter change assessed by diffusion kurtosis imaging of magnetic resonance (MR-DKI) in predicting clinical response to chemotherapy and investigate its prognostic value in patients with colorectal liver metastases (CLM).

Methods

From August 2016 to January 2020, 120 eligible CLM patients were consecutively enrolled in the study. Liver lesions were examined by MR-DKI at baseline and after one cycle of chemotherapy. The texture features were extracted from the D and K map using a prototype postprocessing software. The first 100 cases were utilized as the training set to develop the MR-DKI signature using the R package called “glmnet”, while the remaining 20 cases were used as the validation set. Patients were classified into high-risk and low-risk group according to the risk score, with the cut-off value which was calculated by utilizing ROC analyses. The primary endpoint was the DKI-predicted objective response rate (ORR) of liver metastases, and the secondary endpoints were the DKI-predicted progression-free survival (PFS) and overall survival (OS).

Results

A MRI-DKI signature was constructed using the coefficient value of 6 texture features undergoing the selection by binary logistic regression model with a lasso penalty in the training set. The risk score of each patient was calculated according to the formula (data not published). The AUCs for the signature to predict ORR was 0.818 (95%CI: 0.732-0.905) and 0.790 (95%CI: 0.551-1.029). The DKI-predicted ORRs were 9.5% (4/42) and 72.4% (42/58) in the high-risk and low-risk group, respectively (P<0.05). A worse PFS and OS were observed in high-risk group (all P < 0.05). In the validation set, the predicted ORRs of this signature reached 27.27% (3/11) and 77.78% (7/9) in high-risk and low-risk group, respectively (P=0.07), and worse PFS and OS trends were also shown in the high-risk group, although this was not statistically significant.

Conclusions

The MR-DKI signature could effectively predict the response of hepatic lesions of CLM to chemotherapy earlier than routine scanning.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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