TY - JOUR
T1 - Antiproteinuric effects of renin–angiotensin inhibitors in lung cancer patients receiving bevacizumab
AU - Nihei, Satoru
AU - Sato, Junya
AU - Harada, Toshiyuki
AU - Kuyama, Shoichi
AU - Suzuki, Toshiro
AU - Waga, Nobutsugu
AU - Saito, Yoshitaka
AU - Kisara, Shigeki
AU - Yokota, Atsuko
AU - Okada, Kouji
AU - Tsuchiya, Masami
AU - Terui, Kazufumi
AU - Tadokoro, Yumiko
AU - Chiba, Takeshi
AU - Kudo, Kenzo
AU - Oizumi, Satoshi
AU - Inoue, Akira
AU - Morikawa, Naoto
N1 - Funding Information:
This research study received no specific grant from any funding agency in the public, commercial, or not-for-profit sector. The following principal investigators and institutions contributed to the study: Y. Mori (Iwate Prefectural Central Hospital), H. Yokouchi (Fukushima Medical University Hospital), K. Taima (Hirosaki University Hospital), M. Maemondo (Miyagi Cancer Center), and H. Watanabe (Saka General Hospital).
Publisher Copyright:
© 2018, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2018/6/1
Y1 - 2018/6/1
N2 - Purpose: The objective of this study was to investigate the effect of renin–angiotensin system inhibitors (RASIs) on bevacizumab (BV)-induced proteinuria in non-small cell lung cancer (NSCLC) patients. Materials and methods: We retrospectively reviewed the medical records of NSCLC patients receiving BV between 2008 and 2014 at 11 hospitals. The patients were categorized into three groups according to their antihypertensive drug use: RASI user, non-RASI user, and non-user groups. The primary outcome was a proteinuria event of any grade during the first 6 cycles of BV treatment. Results: A total of 211 patients were included, 89 of whom received antihypertensive drugs. Of these 89 patients, 49 were in the RASI user group, and 40 were in the non-RASI user group. The non-user group comprised 122 patients. The occurrence of proteinuria in the RASI user group was significantly lower than that in the non-RASI user group (P = 0.037) but was not significantly lower than that in the non-user group (P = 0.287). Patients using RASIs had a lower rate of proteinuria than those who did not use RASIs according to multivariate analysis (odds ratio 0.32; 95% confidence interval 0.12–0.86; P = 0.024). Conclusion: Our study suggests that RASI administration reduces the risk of proteinuria in patients receiving BV.
AB - Purpose: The objective of this study was to investigate the effect of renin–angiotensin system inhibitors (RASIs) on bevacizumab (BV)-induced proteinuria in non-small cell lung cancer (NSCLC) patients. Materials and methods: We retrospectively reviewed the medical records of NSCLC patients receiving BV between 2008 and 2014 at 11 hospitals. The patients were categorized into three groups according to their antihypertensive drug use: RASI user, non-RASI user, and non-user groups. The primary outcome was a proteinuria event of any grade during the first 6 cycles of BV treatment. Results: A total of 211 patients were included, 89 of whom received antihypertensive drugs. Of these 89 patients, 49 were in the RASI user group, and 40 were in the non-RASI user group. The non-user group comprised 122 patients. The occurrence of proteinuria in the RASI user group was significantly lower than that in the non-RASI user group (P = 0.037) but was not significantly lower than that in the non-user group (P = 0.287). Patients using RASIs had a lower rate of proteinuria than those who did not use RASIs according to multivariate analysis (odds ratio 0.32; 95% confidence interval 0.12–0.86; P = 0.024). Conclusion: Our study suggests that RASI administration reduces the risk of proteinuria in patients receiving BV.
KW - Bevacizumab
KW - Non-small cell lung cancer
KW - Proteinuria
KW - Renin–angiotensin system inhibitor
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U2 - 10.1007/s00280-018-3580-1
DO - 10.1007/s00280-018-3580-1
M3 - Article
C2 - 29651572
AN - SCOPUS:85045267951
SN - 0344-5704
VL - 81
SP - 1051
EP - 1059
JO - Cancer Chemotherapy and Pharmacology
JF - Cancer Chemotherapy and Pharmacology
IS - 6
ER -