Late adverse effects and quality of life in survivors of testicular germ cell tumour

Standard

Late adverse effects and quality of life in survivors of testicular germ cell tumour. / Chovanec, Michal; Lauritsen, Jakob; Bandak, Mikkel; Oing, Christoph; Kier, Gry Gundgaard; Kreiberg, Michael; Rosenvilde, Josephine; Wagner, Thomas; Bokemeyer, Carsten; Daugaard, Gedske.

In: NAT REV UROL, Vol. 18, No. 4, 04.2021, p. 227-245.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

Harvard

Chovanec, M, Lauritsen, J, Bandak, M, Oing, C, Kier, GG, Kreiberg, M, Rosenvilde, J, Wagner, T, Bokemeyer, C & Daugaard, G 2021, 'Late adverse effects and quality of life in survivors of testicular germ cell tumour', NAT REV UROL, vol. 18, no. 4, pp. 227-245. https://doi.org/10.1038/s41585-021-00440-w, https://doi.org/10.1038/s41585-021-00440-w

APA

Chovanec, M., Lauritsen, J., Bandak, M., Oing, C., Kier, G. G., Kreiberg, M., Rosenvilde, J., Wagner, T., Bokemeyer, C., & Daugaard, G. (2021). Late adverse effects and quality of life in survivors of testicular germ cell tumour. NAT REV UROL, 18(4), 227-245. https://doi.org/10.1038/s41585-021-00440-w, https://doi.org/10.1038/s41585-021-00440-w

Vancouver

Bibtex

@article{72a433543ba84ece84ec3b07fdde1928,
title = "Late adverse effects and quality of life in survivors of testicular germ cell tumour",
abstract = "Currently, ~95% of patients with testicular germ cell tumour (TGCT) are cured, resulting in an increasing number of TGCT survivors. Although cured, these men face potential late adverse effects and reduced quality of life. Survivors face a twofold increased risk of second malignant neoplasms after chemotherapy and radiotherapy, with evidence of dose-dependent associations. For survivors managed with surveillance or treated with radiotherapy, the risk of cardiovascular disease (CVD) is comparable to the risk in the general population, whereas treatment with chemotherapy increases the risk of life-threatening CVD, especially during treatment and after 10 years of follow-up. Other adverse effects are organ-related toxicities such as neuropathy and ototoxicity. Pulmonary and renal impairment in patients with TGCT treated with chemotherapy is limited. Survivors of TGCT might experience psychosocial distress including anxiety disorders, fear of cancer recurrence and TGCT-specific issues, such as sexual dysfunction. Late adverse effects can be avoided in most patients with stage I disease if followed on a surveillance programme. However, patients with disseminated disease can experience toxicities associated with radiotherapy and chemotherapy, and/or adverse effects related to surgery for residual disease. The severity of adverse effects increases with dose of both chemotherapy and radiotherapy. This Review discusses the most recent data concerning the late adverse effects of today's standard treatments for TGCT.",
keywords = "Cancer Survivors, Drug-Related Side Effects and Adverse Reactions, Humans, Male, Neoplasms, Germ Cell and Embryonal/therapy, Orchiectomy/adverse effects, Quality of Life, Radiotherapy/adverse effects, Testicular Neoplasms/therapy, Time Factors",
author = "Michal Chovanec and Jakob Lauritsen and Mikkel Bandak and Christoph Oing and Kier, {Gry Gundgaard} and Michael Kreiberg and Josephine Rosenvilde and Thomas Wagner and Carsten Bokemeyer and Gedske Daugaard",
note = "Publisher Copyright: {\textcopyright} 2021, Springer Nature Limited. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.",
year = "2021",
month = apr,
doi = "10.1038/s41585-021-00440-w",
language = "English",
volume = "18",
pages = "227--245",
journal = "NAT REV UROL",
issn = "1759-4812",
publisher = "NATURE PUBLISHING GROUP",
number = "4",

}

RIS

TY - JOUR

T1 - Late adverse effects and quality of life in survivors of testicular germ cell tumour

AU - Chovanec, Michal

AU - Lauritsen, Jakob

AU - Bandak, Mikkel

AU - Oing, Christoph

AU - Kier, Gry Gundgaard

AU - Kreiberg, Michael

AU - Rosenvilde, Josephine

AU - Wagner, Thomas

AU - Bokemeyer, Carsten

AU - Daugaard, Gedske

N1 - Publisher Copyright: © 2021, Springer Nature Limited. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.

PY - 2021/4

Y1 - 2021/4

N2 - Currently, ~95% of patients with testicular germ cell tumour (TGCT) are cured, resulting in an increasing number of TGCT survivors. Although cured, these men face potential late adverse effects and reduced quality of life. Survivors face a twofold increased risk of second malignant neoplasms after chemotherapy and radiotherapy, with evidence of dose-dependent associations. For survivors managed with surveillance or treated with radiotherapy, the risk of cardiovascular disease (CVD) is comparable to the risk in the general population, whereas treatment with chemotherapy increases the risk of life-threatening CVD, especially during treatment and after 10 years of follow-up. Other adverse effects are organ-related toxicities such as neuropathy and ototoxicity. Pulmonary and renal impairment in patients with TGCT treated with chemotherapy is limited. Survivors of TGCT might experience psychosocial distress including anxiety disorders, fear of cancer recurrence and TGCT-specific issues, such as sexual dysfunction. Late adverse effects can be avoided in most patients with stage I disease if followed on a surveillance programme. However, patients with disseminated disease can experience toxicities associated with radiotherapy and chemotherapy, and/or adverse effects related to surgery for residual disease. The severity of adverse effects increases with dose of both chemotherapy and radiotherapy. This Review discusses the most recent data concerning the late adverse effects of today's standard treatments for TGCT.

AB - Currently, ~95% of patients with testicular germ cell tumour (TGCT) are cured, resulting in an increasing number of TGCT survivors. Although cured, these men face potential late adverse effects and reduced quality of life. Survivors face a twofold increased risk of second malignant neoplasms after chemotherapy and radiotherapy, with evidence of dose-dependent associations. For survivors managed with surveillance or treated with radiotherapy, the risk of cardiovascular disease (CVD) is comparable to the risk in the general population, whereas treatment with chemotherapy increases the risk of life-threatening CVD, especially during treatment and after 10 years of follow-up. Other adverse effects are organ-related toxicities such as neuropathy and ototoxicity. Pulmonary and renal impairment in patients with TGCT treated with chemotherapy is limited. Survivors of TGCT might experience psychosocial distress including anxiety disorders, fear of cancer recurrence and TGCT-specific issues, such as sexual dysfunction. Late adverse effects can be avoided in most patients with stage I disease if followed on a surveillance programme. However, patients with disseminated disease can experience toxicities associated with radiotherapy and chemotherapy, and/or adverse effects related to surgery for residual disease. The severity of adverse effects increases with dose of both chemotherapy and radiotherapy. This Review discusses the most recent data concerning the late adverse effects of today's standard treatments for TGCT.

KW - Cancer Survivors

KW - Drug-Related Side Effects and Adverse Reactions

KW - Humans

KW - Male

KW - Neoplasms, Germ Cell and Embryonal/therapy

KW - Orchiectomy/adverse effects

KW - Quality of Life

KW - Radiotherapy/adverse effects

KW - Testicular Neoplasms/therapy

KW - Time Factors

UR - http://www.scopus.com/inward/record.url?scp=85102350739&partnerID=8YFLogxK

U2 - 10.1038/s41585-021-00440-w

DO - 10.1038/s41585-021-00440-w

M3 - SCORING: Review article

C2 - 33686290

AN - SCOPUS:85102350739

VL - 18

SP - 227

EP - 245

JO - NAT REV UROL

JF - NAT REV UROL

SN - 1759-4812

IS - 4

ER -