2022-RA-1638-ESGO Randomized phase III trial on Niraparib-TSR-042 (dostarlimab) versus physician’s choice in recurrent ovarian, fallopian tube, or primary peritoneal cancer patients not candidate for platinum retreatment: NItCHE trial (MITO 33)
V. Salutari, L. Musacchio, S. Pignata, E. Braicu, D. Cibula, N. Colombo, J. Frenel, S. Giolitto, Floriana Camarda, M. Perri, E. Giudice, G. Scambia, D. Lorusso
{"title":"2022-RA-1638-ESGO Randomized phase III trial on Niraparib-TSR-042 (dostarlimab) versus physician’s choice in recurrent ovarian, fallopian tube, or primary peritoneal cancer patients not candidate for platinum retreatment: NItCHE trial (MITO 33)","authors":"V. Salutari, L. Musacchio, S. Pignata, E. Braicu, D. Cibula, N. Colombo, J. Frenel, S. Giolitto, Floriana Camarda, M. Perri, E. Giudice, G. Scambia, D. Lorusso","doi":"10.1136/ijgc-2022-esgo.762","DOIUrl":null,"url":null,"abstract":"higher FIGO stage(p<0.001), high-grade(p=0.003), serous tumours(p=0.006) and residual tumour as compared to local PC(p<0.001). Wet PC significantly correlated with diffuse localization(p <0.001) and residual tumour as compared to dry PC(p<0.001). Coarse PC was significantly associated with residual tumour as compared to fine PC(p=0.044). Diffuse peritoneal localization(p<0.001), wet PC(p<0.001), and lymph-node involvement(p<0.001) were associated with lower OS and PFS-rates. Conclusion Diffuse PC was a significant predictor of recurrence. Lower OS and PFS were associated with diffuse PC, wet PC, and additional lymph node involvement. Further pro-spective trials are warranted with the inclusion of translational research aspects to better understand the different peritoneal carcinomatosis pattern.","PeriodicalId":89343,"journal":{"name":"Clinical ovarian cancer and other gynecologic malignancies","volume":"43 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical ovarian cancer and other gynecologic malignancies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/ijgc-2022-esgo.762","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
higher FIGO stage(p<0.001), high-grade(p=0.003), serous tumours(p=0.006) and residual tumour as compared to local PC(p<0.001). Wet PC significantly correlated with diffuse localization(p <0.001) and residual tumour as compared to dry PC(p<0.001). Coarse PC was significantly associated with residual tumour as compared to fine PC(p=0.044). Diffuse peritoneal localization(p<0.001), wet PC(p<0.001), and lymph-node involvement(p<0.001) were associated with lower OS and PFS-rates. Conclusion Diffuse PC was a significant predictor of recurrence. Lower OS and PFS were associated with diffuse PC, wet PC, and additional lymph node involvement. Further pro-spective trials are warranted with the inclusion of translational research aspects to better understand the different peritoneal carcinomatosis pattern.