TY - JOUR
T1 - Comparison of bevacizumab alone or with chemotherapy in recurrent ovarian cancer patients
AU - Fuh, Katherine C.
AU - Secord, Angeles A.
AU - Bevis, Kerri S.
AU - Huh, Warner
AU - Elnaggar, Adam
AU - Blansit, Kevin
AU - Previs, Rebecca
AU - Tillmanns, Todd
AU - Kapp, Daniel S.
AU - Chan, John K.
N1 - Publisher Copyright:
© 2015 Elsevier Inc. All rights reserved.
PY - 2015/12/1
Y1 - 2015/12/1
N2 - Background To compare the efficacy of chemotherapy (C) combined with bevacizumab (Bev) versus Bev alone in recurrent, heavily pretreated epithelial ovarian cancer (EOC). Methods A multicenter analysis of patients treated from 2004 to 2011 was performed. Demographic, treatment, response, and adverse event information were obtained. Progression-free (PFS) and overall survival (OS) were analyzed. Results Of 277 patients (median age: 58 years), the majority had Stage III and IV (86%) disease, and 72% had serous histology. 244 (88%) were treated with C + Bev and 33 (12%) with Bev. Corresponding median progression-free survival (PFS) was 8.7 and 6.7 months, and median overall survival (OS) was 14.3 and 10.5 months, respectively. The chemotherapeutic agents combined with Bev and the median OS include: pegylated liposomal doxorubicin (n = 19, OS of 20.4 months), taxanes (n = 55, OS of 20.2 months), gemcitabine (n = 106, OS of 14.1 months), topotecan (n = 43, OS of 13 months), and cyclophosphamide (n = 21, OS of 13 months). There was no significant difference in toxicities between the C + Bev vs. Bev alone group. Conclusion This retrospective analysis supports that combination chemotherapy and bevacizumab prolongs PFS and OS compared with bevacizumab alone.
AB - Background To compare the efficacy of chemotherapy (C) combined with bevacizumab (Bev) versus Bev alone in recurrent, heavily pretreated epithelial ovarian cancer (EOC). Methods A multicenter analysis of patients treated from 2004 to 2011 was performed. Demographic, treatment, response, and adverse event information were obtained. Progression-free (PFS) and overall survival (OS) were analyzed. Results Of 277 patients (median age: 58 years), the majority had Stage III and IV (86%) disease, and 72% had serous histology. 244 (88%) were treated with C + Bev and 33 (12%) with Bev. Corresponding median progression-free survival (PFS) was 8.7 and 6.7 months, and median overall survival (OS) was 14.3 and 10.5 months, respectively. The chemotherapeutic agents combined with Bev and the median OS include: pegylated liposomal doxorubicin (n = 19, OS of 20.4 months), taxanes (n = 55, OS of 20.2 months), gemcitabine (n = 106, OS of 14.1 months), topotecan (n = 43, OS of 13 months), and cyclophosphamide (n = 21, OS of 13 months). There was no significant difference in toxicities between the C + Bev vs. Bev alone group. Conclusion This retrospective analysis supports that combination chemotherapy and bevacizumab prolongs PFS and OS compared with bevacizumab alone.
KW - Bevacizumab
KW - Chemotherapy
KW - Liposomal doxorubicin, taxanes
KW - Platinum-resistant
KW - Recurrent epithelial ovarian cancer
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=84949674322&partnerID=8YFLogxK
U2 - 10.1016/j.ygyno.2015.06.041
DO - 10.1016/j.ygyno.2015.06.041
M3 - Article
C2 - 26144600
AN - SCOPUS:84949674322
SN - 0090-8258
VL - 139
SP - 413
EP - 418
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 3
ER -