Changes in blood pressure during treatment with the tyrosine kinase inhibitor lenvatinib

被引:4
|
作者
Saito, Kei [1 ,2 ]
Fujii, Hideki [1 ,2 ]
Kono, Keiji [1 ,2 ]
Hirabayashi, Ken [1 ,2 ]
Yamatani, Satoshi [1 ,2 ]
Watanabe, Kentaro [1 ,2 ]
Goto, Shunsuke [1 ,2 ]
Komatsu, Shohei [3 ]
Fukumoto, Takumi [3 ]
Nishi, Shinichi [1 ,2 ]
机构
[1] Kobe Univ, Div Nephrol, Grad Sch Med, Kobe, Hyogo, Japan
[2] Kobe Univ, Kidney Ctr, Grad Sch Med, Kobe, Hyogo, Japan
[3] Kobe Univ, Dept Surg, Div Hepatobiliary Pancreat Surg, Grad Sch Med, Kobe, Hyogo, Japan
关键词
ambulatory blood pressure monitoring; blood pressure; lenvatinib; tyrosine kinase inhibitor; urinary sodium excretion; NITRIC-OXIDE; SIGNALING PATHWAY; KIDNEY-DISEASES; VEGF INHIBITION; ADVERSE EVENTS; HYPERTENSION; SUNITINIB; CARCINOMA; ONCONEPHROLOGY; PROTEINURIA;
D O I
10.1093/ckj/sfaa137
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Within the class of tyrosine kinase inhibitors (TKIs), which are used for the treatment of numerous advanced cancers, lenvatinib is associated with a higher prevalence of hypertension (HT) compared with other TKIs. In this study, we investigated the effect of lenvatinib on blood pressure (BP) and associated factors. Methods: This single-centre, retrospective observational study included 25 consecutive patients treated with lenvatinib for unresectable hepatocellular carcinoma from April 2018 to December 2018 at the study institution. We assessed changes in BP using ambulatory BP monitoring, urinary sodium excretion, kidney function, use of antihypertensive agents and diuretics, and fluid retention following treatment initiation with lenvatinib. Results: At 1week after treatment initiation, the mean BP and the percentage of patients with riser pattern significantly increased compared with those at the baseline. Although there were no significant changes at 1 week, urinary sodium excretion (153.451.7 and 112.5 +/- 65.0 mEq/day at 1 and 3 weeks, respectively, P<0.05) and estimated glomerular filtration rate significantly decreased and the number of patients with fluid retention increased at 3 weeks. Furthermore, patients with fluid retention had significantly higher BP or required more intensive BP treatment compared with those without fluid retention. Conclusions: Lenvatinib might lead to HT without fluid retention soon after the initiation of treatment, subsequently leading to a reduction in urinary sodium excretion, thereby contributing to a rise in BP by fluid retention.
引用
收藏
页码:325 / 331
页数:7
相关论文
共 50 条
  • [31] Hypothyroidism during treatment with tyrosine kinase inhibitors
    Zygulska, Aneta L.
    Krzemieniecki, Krzysztof
    Sowa-Staszczak, Anna
    ENDOKRYNOLOGIA POLSKA, 2012, 63 (04) : 302 - 306
  • [32] Lenvatinib and other tyrosine kinase inhibitors for the treatment of radioiodine refractory, advanced, and progressive thyroid cancer
    Lorusso, Loredana
    Pieruzzi, Letizia
    Biagini, Agnese
    Sabini, Elena
    Valerio, Laura
    Giani, Carlotta
    Passannanti, Paolo
    Pontillo-Contillo, Benedetta
    Battaglia, Valentina
    Mazzeo, Salvatore
    Molinaro, Eleonora
    Elisei, Rossella
    ONCOTARGETS AND THERAPY, 2016, 9 : 6467 - 6477
  • [33] Thoracoscopic lobectomy following neoadjuvant tyrosine kinase inhibitor treatment
    Chudgar, Neel P.
    Jones, David R.
    JTCVS TECHNIQUES, 2021, 7 : 294 - 297
  • [34] A phase 1 study of lenvatinib, multiple receptor tyrosine kinase inhibitor, in Japanese patients with advanced solid tumors
    Nakamichi, Shinji
    Nokihara, Hiroshi
    Yamamoto, Noboru
    Yamada, Yasuhide
    Honda, Kazunori
    Tamura, Yosuke
    Wakui, Hiroshi
    Sasaki, Tatsuya
    Yusa, Wataru
    Fujino, Katsuki
    Tamura, Tomohide
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2015, 76 (06) : 1153 - 1161
  • [35] A phase 1 study of lenvatinib, multiple receptor tyrosine kinase inhibitor, in Japanese patients with advanced solid tumors
    Shinji Nakamichi
    Hiroshi Nokihara
    Noboru Yamamoto
    Yasuhide Yamada
    Kazunori Honda
    Yosuke Tamura
    Hiroshi Wakui
    Tatsuya Sasaki
    Wataru Yusa
    Katsuki Fujino
    Tomohide Tamura
    Cancer Chemotherapy and Pharmacology, 2015, 76 : 1153 - 1161
  • [36] Is There Still a Place for Tyrosine Kinase Inhibitors for the Treatment of Hepatocellular Carcinoma at the Time of Immunotherapies? A Focus on Lenvatinib
    Decraecker, Marie
    Toulouse, Caroline
    Blanc, Jean-Frederic
    CANCERS, 2021, 13 (24)
  • [38] Clinical Pharmacokinetic and Pharmacodynamic Profile of Lenvatinib, an Orally Active, Small-Molecule, Multitargeted Tyrosine Kinase Inhibitor
    Hussein, Ziad
    Mizuo, Hitoshi
    Hayato, Seiichi
    Namiki, Masayuki
    Shumaker, Robert
    EUROPEAN JOURNAL OF DRUG METABOLISM AND PHARMACOKINETICS, 2017, 42 (06) : 903 - 914
  • [39] Treatment of polycystic kidney disease with a novel tyrosine kinase inhibitor
    Sweeney, WE
    Chen, YG
    Nakanishi, K
    Frost, P
    Avner, ED
    KIDNEY INTERNATIONAL, 2000, 57 (01) : 33 - 40
  • [40] Exacerbation of psoriasis after treatment with an EGFR tyrosine kinase inhibitor
    Zorzou, MP
    Stratigos, A
    Efstathiou, E
    Bamias, A
    ACTA DERMATO-VENEREOLOGICA, 2004, 84 (04) : 308 - 309