OP008/#194 P53ABN molecular subtype encompasses a morphologically diverse subset of endometrial cancers and identifies therapeutic opportunities to improve outcomes

A. Jamieson, E. Thompson, J. Huvila, S. Leung, A. Lum, L. Helpman, S. Salvador, J. Irving, K. Grondin, A. Lytwyn, C. Parra-Herran, S. Offman, M. Kinloch, M. Plante, D. Vicus, A. Talhouk, S. Scott, D. Huntsman, C. Gilks, J. Mcalpine
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Abstract

ract (7%), lymphopenia (7%), thrombocytopenia (7%), weight loss (7%), hypokalemia (7%). Sixteen patients are currently evaluable for response; 6 (37.5%) with PR, 8 (50%) SD, 2 (12.5%) PD; ORR 33% (4/12) in ovarian cancer and 50% (2/ 4) in endometrial cancer. Median PFS is 6.3 months with 95%CI (0.7, 13.8) months. Conclusions Combination rucaparib and MIRV was tolerable with mostly manageable side effects and encouraging activity in this heavily pretreated population (including prior PARPi) of both endometrial and ovarian cancer.
OP008/#194 P53ABN分子亚型涵盖了子宫内膜癌的形态多样化亚群,并确定了改善预后的治疗机会
Ract(7%),淋巴细胞减少(7%),血小板减少(7%),体重减轻(7%),低钾血症(7%)。目前有16名患者可评估反应;PR 6例(37.5%),SD 8例(50%),PD 2例(12.5%);卵巢癌的ORR为33%(4/12),子宫内膜癌为50%(2/ 4)。中位PFS为6.3个月,95%CI(0.7, 13.8)个月。结论:鲁卡帕尼和MIRV联合用药在重度预处理的子宫内膜癌和卵巢癌患者(包括PARPi患者)中是可耐受的,副作用大多可控,并且具有促进活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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