Multimodality MRI-based radiomics approach to predict the posttreatment response of lung cancer brain metastases to gamma knife radiosurgery
Objectives To develop and validate a multimodality MRI-based radiomics approach to predicting the posttreatment response of lung cancer brain metastases (LCBM) to gamma knife radiosurgery (GKRS). Methods We retrospectively analyzed 213 lesions from 137 patients with LCBM who received GKRS between Ja...
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Veröffentlicht in: | European radiology 2022-04, Vol.32 (4), p.2266-2276 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Objectives
To develop and validate a multimodality MRI-based radiomics approach to predicting the posttreatment response of lung cancer brain metastases (LCBM) to gamma knife radiosurgery (GKRS).
Methods
We retrospectively analyzed 213 lesions from 137 patients with LCBM who received GKRS between January 2017 and November 2020. The data were divided into a primary cohort (102 patients with 173 lesions) and an independent validation cohort (35 patients with 40 lesions) according to the time of treatment. Benefit result was defined using pretreatment and 3-month follow-up MRI images based on the Response Assessment in Neuro-Oncology Brain Metastases criteria. Valuable radiomics features were extracted from pretreatment multimodality MRI images using random forests. Prediction performance among the radiomics features of tumor core (RFTC) and radiomics features of peritumoral edema (RFPE) together was evaluated separately. Then, the random forest radiomics score and nomogram were developed through the primary cohort and evaluated through an independent validation cohort. Prediction performance was evaluated by ROC curve, calibration curve, and decision curve.
Results
Gender (
p
= 0.018), histological subtype (
p
= 0.009), epidermal growth factor receptor mutation (
p
= 0.034), and targeted drug treatment (
p
= 0.021) were significantly associated with posttreatment response. Adding RFPE to RFTC showed improved prediction performance than RFTC alone in primary cohort (AUC = 0.848 versus AUC = 0.750;
p
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ISSN: | 0938-7994 1432-1084 |
DOI: | 10.1007/s00330-021-08368-w |