Prognostic impact of erythropoietin‐stimulating agent use during front‐line chemotherapy in patients with ovarian cancer: A Korean multicenter cohort study

Author:

Shim Seung‐Hyuk1,Yang Eun‐Jung2,Jang Eun Bi1,Lee Seungjun3,Kim Hee Seung4,Shin Yoon‐Kyung5,Lee Shin‐Wha5,Chang Chi‐Son6,Song Heekyoung7,Lee Sung Jong7,Kim Jeeyeon8,Chang Suk‐Joon8,Lim Myong Cheol910,Choi Chel Hun6

Affiliation:

1. Department of Obstetrics and Gynecology, Research Institute of Medical Science Konkuk University School of Medicine Seoul Republic of Korea

2. Department of Obstetrics and Gynecology Soonchunhyang University Cheonan Hospital Cheonan South Chungcheong Republic of Korea

3. Department of Obstetrics and Gynecology Seoul National University Hospital Seoul Republic of Korea

4. Department of Obstetrics and Gynecology Seoul National University College of Medicine Seoul Republic of Korea

5. Department of Obstetrics and Gynecology Asan Medical Center, University of Ulsan College of Medicine Seoul Republic of Korea

6. Department of Obstetrics and Gynecology Samsung Medical Center, Sungkyunkwan University School of Medicine Seoul Republic of Korea

7. Department of Obstetrics and Gynecology, Seoul St. Mary's Hospital, College of Medicine The Catholic University of Korea Seoul Republic of Korea

8. Department of Obstetrics and Gynecology, Gynecologic Cancer Center Ajou University School of Medicine Suwon Republic of Korea

9. Center for Gynecologic Cancer and Center for Clinical Trial, National Cancer Center Goyang Korea

10. Division of Tumor Immunology Research Institute and Hospital, National Cancer Center Goyang Korea

Abstract

AbstractObjectiveTo evaluate whether treatment with erythropoiesis‐stimulating agents (ESAs) for chemotherapy‐induced anemia affects progression‐free survival (PFS) in patients receiving front‐line chemotherapy following surgery for ovarian cancer (OC).MethodsWe retrospectively reviewed all consecutive patients who received front‐line chemotherapy after surgery between 2013 and 2019 at six institutions. The patients were divided according to the use of ESAs during front‐line chemotherapy. The primary endpoint was PFS. The secondary endpoint was the occurrence of thromboembolism. Propensity score matching (PSM) analysis was used to compare survival between matched cohorts.ResultsOverall, 2147 patients (433 receiving ESA and 1714 for no‐ESA) were identified, with a median follow‐up of 44.0 months. The ESA group showed a significantly higher proportion of stage III/IV disease (81.8% vs 61.1%; P < 0.001) and postoperative gross residual disease (32.3% vs 21.2%; P < 0.001) than the no‐ESA group. In the multivariable Cox regression analysis, the use of ESAs did not affect PFS (adjusted hazard ratio, 1.03; 95% confidence interval [CI]: 0.89–1.20; P = 0.661). The incidence of thromboembolism was 10.2% in the ESA group and 4.6% in the no‐ESA group (adjusted odds ratio, 6.58; 95% CI: 3.26–13.28; P < 0.001). When comparing the well‐matched cohorts after PSM, PFS did not differ between the ESA (median PFS 23.5 months) and no‐ESA groups (median PFS 22.2 months) (P = 0.540, log‐rank test).ConclusionsThe use of ESAs during front‐line chemotherapy did not negatively affect PFS in patients with OC after surgery but increased the risk of thromboembolism.

Publisher

Wiley

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