Subsequent therapies and survival after immunotherapy in recurrent ovarian cancer

التفاصيل البيبلوغرافية
العنوان: Subsequent therapies and survival after immunotherapy in recurrent ovarian cancer
المؤلفون: Jason A. Konner, Ying L Liu, Vivian N. Emengo, Roisin E. O'Cearbhaill, Carol Aghajanian, Dmitriy Zamarin, Alexia Iasonos, Claire F. Friedman, Qin Zhou
المصدر: Gynecol Oncol
بيانات النشر: Elsevier BV, 2019.
سنة النشر: 2019
مصطلحات موضوعية: Adult, 0301 basic medicine, Oncology, medicine.medical_specialty, Bevacizumab, medicine.medical_treatment, Immune checkpoint inhibitors, Programmed Cell Death 1 Receptor, Population, New York, Kaplan-Meier Estimate, Carcinoma, Ovarian Epithelial, Article, B7-H1 Antigen, Young Adult, 03 medical and health sciences, Antineoplastic Agents, Immunological, 0302 clinical medicine, Internal medicine, Antineoplastic Combined Chemotherapy Protocols, polycyclic compounds, medicine, Humans, CTLA-4 Antigen, education, Survival analysis, Aged, Retrospective Studies, Ovarian Neoplasms, education.field_of_study, Chemotherapy, business.industry, Proportional hazards model, Obstetrics and Gynecology, Immunotherapy, Middle Aged, medicine.disease, 030104 developmental biology, 030220 oncology & carcinogenesis, Female, Neoplasm Recurrence, Local, business, Ovarian cancer, hormones, hormone substitutes, and hormone antagonists, medicine.drug
الوصف: OBJECTIVES: Immune checkpoint inhibitors (ICIs) have modest activity in ovarian cancer (OC), yet little is known about their effects on subsequent treatment. Preclinical studies suggest immunotherapy may enhance response to chemotherapy. We sought to evaluate the impact of ICIs on subsequent therapies and survival in recurrent OC. METHODS: A retrospective review was conducted to identify women with recurrent OC who received ICI from 01/2013–5/2017 and ≥1 subsequent treatment. Treatment duration after ICI was calculated using time-to-event analysis. Kaplan-Meier survival analysis and Cox proportional hazards models were used to calculate overall survival (OS) from first treatment after ICI and to assess survival differences by clinical benefit from ICI, defined by long (≥24 weeks) versus short (
تدمد: 0090-8258
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5c97d57beade09b491c8f727c1897bbTest
https://doi.org/10.1016/j.ygyno.2019.08.006Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....f5c97d57beade09b491c8f727c1897bb
قاعدة البيانات: OpenAIRE