TY - JOUR
T1 - Hypertension and Prohypertensive Antineoplastic Therapies in Cancer Patients
AU - Van Dorst, Daan C.H.
AU - Dobbin, Stephen J.H.
AU - Neves, Karla B.
AU - Herrmann, Joerg
AU - Herrmann, Sandra M.
AU - Versmissen, Jorie
AU - Mathijssen, Ron H.J.
AU - Danser, A. H.Jan
AU - Lang, Ninian N.
N1 - Funding Information:
S.J.H. Dobbin, K.B. Neves, and N.N. Lang are supported by a British Heart Foundation (BHF) Centre of Research Excellence grant (RE/18/6/34217) and a BHF Project Grant (PG/19/64/34434). S.M. Hermann is supported by National Institutes of Health K08 DK118120 from the NIDDK.
Publisher Copyright:
© 2020 American Heart Association, Inc.
PY - 2021/4/2
Y1 - 2021/4/2
N2 - The development of a wide range of novel antineoplastic therapies has improved the prognosis for patients with a wide range of malignancies, which has increased the number of cancer survivors substantially. Despite the oncological benefit, cancer survivors are exposed to short- and long-term adverse cardiovascular toxicities associated with anticancer therapies. Systemic hypertension, the most common comorbidity among cancer patients, is a major contributor to the increased risk for developing these adverse cardiovascular events. Cancer and hypertension have common risk factors, have overlapping pathophysiological mechanisms and hypertension may also be a risk factor for some tumor types. Many cancer therapies have prohypertensive effects. Although some of the mechanisms by which these antineoplastic agents lead to hypertension have been characterized, further preclinical and clinical studies are required to investigate the exact pathophysiology and the optimal management of hypertension associated with anticancer therapy. In this way, monitoring and management of hypertension before, during, and after cancer treatment can be improved to minimize cardiovascular risks. This is vital to optimize cardiovascular health in patients with cancer and survivors, and to ensure that advances in terms of cancer survivorship do not come at the expense of increased cardiovascular toxicities.
AB - The development of a wide range of novel antineoplastic therapies has improved the prognosis for patients with a wide range of malignancies, which has increased the number of cancer survivors substantially. Despite the oncological benefit, cancer survivors are exposed to short- and long-term adverse cardiovascular toxicities associated with anticancer therapies. Systemic hypertension, the most common comorbidity among cancer patients, is a major contributor to the increased risk for developing these adverse cardiovascular events. Cancer and hypertension have common risk factors, have overlapping pathophysiological mechanisms and hypertension may also be a risk factor for some tumor types. Many cancer therapies have prohypertensive effects. Although some of the mechanisms by which these antineoplastic agents lead to hypertension have been characterized, further preclinical and clinical studies are required to investigate the exact pathophysiology and the optimal management of hypertension associated with anticancer therapy. In this way, monitoring and management of hypertension before, during, and after cancer treatment can be improved to minimize cardiovascular risks. This is vital to optimize cardiovascular health in patients with cancer and survivors, and to ensure that advances in terms of cancer survivorship do not come at the expense of increased cardiovascular toxicities.
KW - angiogenesis inhibitors
KW - antineoplastic agents
KW - comorbidity
KW - hypertension
KW - neoplasms
KW - prognosis
KW - risk factors
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U2 - 10.1161/CIRCRESAHA.121.318051
DO - 10.1161/CIRCRESAHA.121.318051
M3 - Article
C2 - 33793337
AN - SCOPUS:85103806735
SN - 0009-7330
VL - 128
SP - 1040
EP - 1061
JO - Circulation research
JF - Circulation research
IS - 7
ER -