Personalizing, not patronizing: the case for patient autonomy by unbiased presentation of management options in stage I testicular cancer

Standard

Personalizing, not patronizing: the case for patient autonomy by unbiased presentation of management options in stage I testicular cancer. / Oldenburg, J; Aparicio, J; Beyer, J; Cohn-Cedermark, G; Cullen, M; Gilligan, T; De Giorgi, U; De Santis, M; de Wit, R; Fosså, S D; Germà-Lluch, J R; Gillessen, S; Haugnes, H S; Honecker, F; Horwich, A; Lorch, A; Ondruš, D; Rosti, G; Stephenson, A J; Tandstad, T; SWENOTECA (Swedish Norwegian Testicular Cancer group), the Italian Germ Cell Cancer Group (IGG), Spanish Germ Cell Cancer Group (SGCCG).

in: ANN ONCOL, Jahrgang 26, Nr. 5, 01.05.2015, S. 833-838.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Oldenburg, J, Aparicio, J, Beyer, J, Cohn-Cedermark, G, Cullen, M, Gilligan, T, De Giorgi, U, De Santis, M, de Wit, R, Fosså, SD, Germà-Lluch, JR, Gillessen, S, Haugnes, HS, Honecker, F, Horwich, A, Lorch, A, Ondruš, D, Rosti, G, Stephenson, AJ, Tandstad, T & SWENOTECA (Swedish Norwegian Testicular Cancer group), the Italian Germ Cell Cancer Group (IGG), Spanish Germ Cell Cancer Group (SGCCG) 2015, 'Personalizing, not patronizing: the case for patient autonomy by unbiased presentation of management options in stage I testicular cancer', ANN ONCOL, Jg. 26, Nr. 5, S. 833-838. https://doi.org/10.1093/annonc/mdu514

APA

Oldenburg, J., Aparicio, J., Beyer, J., Cohn-Cedermark, G., Cullen, M., Gilligan, T., De Giorgi, U., De Santis, M., de Wit, R., Fosså, S. D., Germà-Lluch, J. R., Gillessen, S., Haugnes, H. S., Honecker, F., Horwich, A., Lorch, A., Ondruš, D., Rosti, G., Stephenson, A. J., ... SWENOTECA (Swedish Norwegian Testicular Cancer group), the Italian Germ Cell Cancer Group (IGG), Spanish Germ Cell Cancer Group (SGCCG) (2015). Personalizing, not patronizing: the case for patient autonomy by unbiased presentation of management options in stage I testicular cancer. ANN ONCOL, 26(5), 833-838. https://doi.org/10.1093/annonc/mdu514

Vancouver

Bibtex

@article{ca39d67cee9d430bb2f046cb87eaed05,
title = "Personalizing, not patronizing: the case for patient autonomy by unbiased presentation of management options in stage I testicular cancer",
abstract = "Testicular cancer (TC) is the most common neoplasm in males aged 15-40 years. The majority of patients have no evidence of metastases at diagnosis and thus have clinical stage I (CSI) disease [Oldenburg J, Fossa SD, Nuver J et al. Testicular seminoma and non-seminoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2013; 24(Suppl 6): vi125-vi132; de Wit R, Fizazi K. Controversies in the management of clinical stage I testis cancer. J Clin Oncol 2006; 24: 5482-5492.]. Management of CSI TC is controversial and options include surveillance and active treatment. Different forms of adjuvant therapy exist, including either one or two cycles of carboplatin chemotherapy or radiotherapy for seminoma and either one or two cycles of cisplatin-based chemotherapy or retroperitoneal lymph node dissection for non-seminoma. Long-term disease-specific survival is ∼99% with any of these approaches, including surveillance. While surveillance allows most patients to avoid additional treatment, adjuvant therapy markedly lowers the relapse rate. Weighing the net benefits of surveillance against those of adjuvant treatment depends on prioritizing competing aims such as avoiding unnecessary treatment, avoiding more burdensome treatment with salvage chemotherapy and minimizing the anxiety, stress and life disruption associated with relapse. Unbiased information about the advantages and disadvantages of surveillance and adjuvant treatment is a prerequisite for informed consent by the patient. In a clinical scenario like CSI TC, where different disease-management options produce indistinguishable long-term survival rates, patient values, priorities and preferences should be taken into account. In this review, we provide an overview about risk factors for relapse, potential benefits and harms of adjuvant chemotherapy and active surveillance and a rationale for involving patients in individualized decision making about their treatment rather than adopting a uniform recommendation for all.",
author = "J Oldenburg and J Aparicio and J Beyer and G Cohn-Cedermark and M Cullen and T Gilligan and {De Giorgi}, U and {De Santis}, M and {de Wit}, R and Foss{\aa}, {S D} and Germ{\`a}-Lluch, {J R} and S Gillessen and Haugnes, {H S} and F Honecker and A Horwich and A Lorch and D Ondru{\v s} and G Rosti and Stephenson, {A J} and T Tandstad and {SWENOTECA (Swedish Norwegian Testicular Cancer group), the Italian Germ Cell Cancer Group (IGG), Spanish Germ Cell Cancer Group (SGCCG)}",
note = "{\textcopyright} The Author 2014. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.",
year = "2015",
month = may,
day = "1",
doi = "10.1093/annonc/mdu514",
language = "English",
volume = "26",
pages = "833--838",
journal = "ANN ONCOL",
issn = "0923-7534",
publisher = "Oxford University Press",
number = "5",

}

RIS

TY - JOUR

T1 - Personalizing, not patronizing: the case for patient autonomy by unbiased presentation of management options in stage I testicular cancer

AU - Oldenburg, J

AU - Aparicio, J

AU - Beyer, J

AU - Cohn-Cedermark, G

AU - Cullen, M

AU - Gilligan, T

AU - De Giorgi, U

AU - De Santis, M

AU - de Wit, R

AU - Fosså, S D

AU - Germà-Lluch, J R

AU - Gillessen, S

AU - Haugnes, H S

AU - Honecker, F

AU - Horwich, A

AU - Lorch, A

AU - Ondruš, D

AU - Rosti, G

AU - Stephenson, A J

AU - Tandstad, T

AU - SWENOTECA (Swedish Norwegian Testicular Cancer group), the Italian Germ Cell Cancer Group (IGG), Spanish Germ Cell Cancer Group (SGCCG)

N1 - © The Author 2014. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

PY - 2015/5/1

Y1 - 2015/5/1

N2 - Testicular cancer (TC) is the most common neoplasm in males aged 15-40 years. The majority of patients have no evidence of metastases at diagnosis and thus have clinical stage I (CSI) disease [Oldenburg J, Fossa SD, Nuver J et al. Testicular seminoma and non-seminoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2013; 24(Suppl 6): vi125-vi132; de Wit R, Fizazi K. Controversies in the management of clinical stage I testis cancer. J Clin Oncol 2006; 24: 5482-5492.]. Management of CSI TC is controversial and options include surveillance and active treatment. Different forms of adjuvant therapy exist, including either one or two cycles of carboplatin chemotherapy or radiotherapy for seminoma and either one or two cycles of cisplatin-based chemotherapy or retroperitoneal lymph node dissection for non-seminoma. Long-term disease-specific survival is ∼99% with any of these approaches, including surveillance. While surveillance allows most patients to avoid additional treatment, adjuvant therapy markedly lowers the relapse rate. Weighing the net benefits of surveillance against those of adjuvant treatment depends on prioritizing competing aims such as avoiding unnecessary treatment, avoiding more burdensome treatment with salvage chemotherapy and minimizing the anxiety, stress and life disruption associated with relapse. Unbiased information about the advantages and disadvantages of surveillance and adjuvant treatment is a prerequisite for informed consent by the patient. In a clinical scenario like CSI TC, where different disease-management options produce indistinguishable long-term survival rates, patient values, priorities and preferences should be taken into account. In this review, we provide an overview about risk factors for relapse, potential benefits and harms of adjuvant chemotherapy and active surveillance and a rationale for involving patients in individualized decision making about their treatment rather than adopting a uniform recommendation for all.

AB - Testicular cancer (TC) is the most common neoplasm in males aged 15-40 years. The majority of patients have no evidence of metastases at diagnosis and thus have clinical stage I (CSI) disease [Oldenburg J, Fossa SD, Nuver J et al. Testicular seminoma and non-seminoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2013; 24(Suppl 6): vi125-vi132; de Wit R, Fizazi K. Controversies in the management of clinical stage I testis cancer. J Clin Oncol 2006; 24: 5482-5492.]. Management of CSI TC is controversial and options include surveillance and active treatment. Different forms of adjuvant therapy exist, including either one or two cycles of carboplatin chemotherapy or radiotherapy for seminoma and either one or two cycles of cisplatin-based chemotherapy or retroperitoneal lymph node dissection for non-seminoma. Long-term disease-specific survival is ∼99% with any of these approaches, including surveillance. While surveillance allows most patients to avoid additional treatment, adjuvant therapy markedly lowers the relapse rate. Weighing the net benefits of surveillance against those of adjuvant treatment depends on prioritizing competing aims such as avoiding unnecessary treatment, avoiding more burdensome treatment with salvage chemotherapy and minimizing the anxiety, stress and life disruption associated with relapse. Unbiased information about the advantages and disadvantages of surveillance and adjuvant treatment is a prerequisite for informed consent by the patient. In a clinical scenario like CSI TC, where different disease-management options produce indistinguishable long-term survival rates, patient values, priorities and preferences should be taken into account. In this review, we provide an overview about risk factors for relapse, potential benefits and harms of adjuvant chemotherapy and active surveillance and a rationale for involving patients in individualized decision making about their treatment rather than adopting a uniform recommendation for all.

U2 - 10.1093/annonc/mdu514

DO - 10.1093/annonc/mdu514

M3 - SCORING: Journal article

C2 - 25378299

VL - 26

SP - 833

EP - 838

JO - ANN ONCOL

JF - ANN ONCOL

SN - 0923-7534

IS - 5

ER -