TY - JOUR
T1 - Efficacy of stereotactic body radiotherapy and response prediction using artificial intelligence in oligometastatic gynaecologic cancer
AU - Macchia, Gabriella
AU - Cilla, Savino
AU - Pezzulla, Donato
AU - Campitelli, Maura
AU - Laliscia, Concetta
AU - Lazzari, Roberta
AU - Draghini, Lorena
AU - Fodor, Andrei
AU - D'Agostino, Giuseppe R
AU - Russo, Donatella
AU - Balcet, Vittoria
AU - Ferioli, Martina
AU - Vicenzi, Lisa
AU - Raguso, Arcangela
AU - Di Cataldo, Vanessa
AU - Perrucci, Elisabetta
AU - Borghesi, Simona
AU - Ippolito, Edy
AU - Gentile, Piercarlo
AU - De Sanctis, Vitaliana
AU - Titone, Francesca
AU - Delle Curti, Clelia Teresa
AU - Huscher, Alessandra
AU - Gambacorta, Maria Antonietta
AU - Ferrandina, Maria Gabriella
AU - Morganti, Alessio G
AU - Deodato, Francesco
PY - 2024
Y1 - 2024
N2 - Purpose: We present a large real-world multicentric dataset of ovarian, uterine and cervical oligometastatic lesions treated with SBRT exploring efficacy and clinical outcomes. In addition, an exploratory machine learning analysis was performed. Methods: A pooled analysis of gynecological oligometastases in terms of efficacy and clinical outcomes as well an exploratory machine learning model to predict the CR to SBRT were carried out. The CR rate following radiotherapy (RT) was the study main endpoint. The secondary endpoints included the 2-year actuarial LC, DMFS, PFS, and OS. Results: 501 patients from 21 radiation oncology institutions with 846 gynecological metastases were analyzed, mainly ovarian (53.1%) and uterine metastases(32.1%).Multiple fraction radiotherapy was used in 762 metastases(90.1%).The most frequent schedule was 24 Gy in 3 fractions(13.4%). CR was observed in 538(63.7%) lesions. The Machine learning analysis showed a poor ability to find covariates strong enough to predict CR in the whole series. Analyzing them separately, in uterine cancer, if RT dose≥78.3Gy, the CR probability was 75.4%; if volume was <13.7 cc, the CR probability became 85.1%. In ovarian cancer, if the lesion was a lymph node, the CR probability was 71.4%; if volume was <17 cc, the CR probability rose to 78.4%. No covariate predicted the CR for cervical lesions. The overall 2-year actuarial LC was 79.2%, however it was 91.5% for CR and 52.5% for not CR lesions(p < 0.001). The overall 2-year DMFS, PFS and OS rate were 27.3%, 24.8% and 71.0%, with significant differences between CR and not CR. Conclusions: CR was substantially associated to patient outcomes in our series of gynecological cancer oligometastatic lesions. The ability to predict a CR through artificial intelligence could also drive treatment choices in the context of personalized oncology.
AB - Purpose: We present a large real-world multicentric dataset of ovarian, uterine and cervical oligometastatic lesions treated with SBRT exploring efficacy and clinical outcomes. In addition, an exploratory machine learning analysis was performed. Methods: A pooled analysis of gynecological oligometastases in terms of efficacy and clinical outcomes as well an exploratory machine learning model to predict the CR to SBRT were carried out. The CR rate following radiotherapy (RT) was the study main endpoint. The secondary endpoints included the 2-year actuarial LC, DMFS, PFS, and OS. Results: 501 patients from 21 radiation oncology institutions with 846 gynecological metastases were analyzed, mainly ovarian (53.1%) and uterine metastases(32.1%).Multiple fraction radiotherapy was used in 762 metastases(90.1%).The most frequent schedule was 24 Gy in 3 fractions(13.4%). CR was observed in 538(63.7%) lesions. The Machine learning analysis showed a poor ability to find covariates strong enough to predict CR in the whole series. Analyzing them separately, in uterine cancer, if RT dose≥78.3Gy, the CR probability was 75.4%; if volume was <13.7 cc, the CR probability became 85.1%. In ovarian cancer, if the lesion was a lymph node, the CR probability was 71.4%; if volume was <17 cc, the CR probability rose to 78.4%. No covariate predicted the CR for cervical lesions. The overall 2-year actuarial LC was 79.2%, however it was 91.5% for CR and 52.5% for not CR lesions(p < 0.001). The overall 2-year DMFS, PFS and OS rate were 27.3%, 24.8% and 71.0%, with significant differences between CR and not CR. Conclusions: CR was substantially associated to patient outcomes in our series of gynecological cancer oligometastatic lesions. The ability to predict a CR through artificial intelligence could also drive treatment choices in the context of personalized oncology.
KW - Female
KW - Genital Neoplasms
KW - Female
KW - Genital Neoplasms
UR - https://publicatt.unicatt.it/handle/10807/303487
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85183176057&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85183176057&origin=inward
U2 - 10.1016/j.ygyno.2024.01.023
DO - 10.1016/j.ygyno.2024.01.023
M3 - Article
SN - 1095-6859
VL - 184
SP - 16
EP - 23
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - MAY
ER -