Abstract
Background: Ongoing research in the field of both localized, locally advanced and metastatic renal cell carcinoma has resulted in the availability of multiple treatment options. Hence, many questions are still unanswered and await further research. A nationwide collaborative registry allows to collect corresponding data. For this purpose, the Dutch PROspective Renal Cell Carcinoma cohort (PRO-RCC) has been founded, for the prospective collection of long-term clinical data, patient reported outcome measures (PROMs) and patient reported experience measures (PREMs). Methods: PRO-RCC is designed as a multicenter cohort for all Dutch patients with renal cell carcinoma (RCC). Recruitment will start in the Netherlands in 2023. Importantly, participants may also consent to participation in a ‘Trial within cohorts’ studies (TwiCs). The TwiCs design provides a method to perform (randomized) interventional studies within the registry. The clinical data collection is embedded in the Netherlands Cancer Registry (NCR). Next to the standardly available data on RCC, additional clinical data will be collected. PROMS entail Health-Related Quality of Life (HRQoL), symptom monitoring with optional ecological momentary assessment (EMA) of pain and fatigue, and optional return to work- and/or nutrition questionnaires. PREMS entail satisfaction with care. Both PROMS and PREMS are collected through the PROFILES registry and are accessible for the patient and the treating physician. Trial registration: Ethical board approval has been obtained (2021_218) and the study has been registered at ClinicalTrials.gov (NCT05326620). Discussion: PRO-RCC is a nationwide long-term cohort for the collection of real-world clinical data, PROMS and PREMS. By facilitating an infrastructure for the collection of prospective data on RCC, PRO-RCC will contribute to observational research in a real-world study population and prove effectiveness in daily clinical practice. The infrastructure of this cohort also enables that interventional studies can be conducted with the TwiCs design, without the disadvantages of classic RCTs such as slow patient accrual and risk of dropping out after randomization.
Original language | English |
---|---|
Article number | 648 |
Journal | BMC Cancer |
Volume | 23 |
Issue number | 1 |
DOIs | |
Publication status | Published - 11 Jul 2023 |
Bibliographical note
Funding Information:
We would like to thank the Profiles Registry advisory board , the Dutch Federation of Cancer Patient Organizations (NFK), the Dutch patient association of bladder or kidney cancer (”Leven met Blaas- of Nierkanker”) for their contribution in the design of the cohort. We would like to thank the following experts on their contribution in the design of the cohort: Nutrition: Dr. A. Vrieling, Dr. S. Beijer. EMA: dr. B. de Rooij en prof. M. van der Lee for the EMA expertise. Cost-effectiveness: Dr. S. de Groot. Return to work: Prof. A. de Boer, Dr. S. Duijts.
Funding:
To date, PRO-RCC received funding for the set-up and maintenance of the
infrastructure from MSD, Ipsen and Bristol Myers Squibb. The funding parties
did not contribute to the study design or the manuscript.
Award/grant number: N/A.
Publisher Copyright:
© 2023, The Author(s).
Access to Document
10.1186/s12885-023-11094-9Licence: CC BY
The PRO-RCC study a long-term PROspective Renal Cell Carcinoma cohort in the Netherlands, providing an infrastructure for ‘Trial within Cohorts’ study designsFinal published version, 0.98 MBLicence: CC BY
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Yildirim, H., Widdershoven, C. V., Aarts, M. J., Bex, A., Bloemendal, H. J., Bochove-Overgaauw, D. M., Hamberg, P., Herbschleb, K. H., van der Hulle, T., Lagerveld, B. W., van Oijen, M. G., Oosting, S. F., van Thienen, J. V., van der Veldt, A. A., Westgeest, H. M., Zeijdner, E. E., Aben, K. K., van den Hurk, C., Zondervan, P. J., & Bins, A. D. (2023). The PRO-RCC study: a long-term PROspective Renal Cell Carcinoma cohort in the Netherlands, providing an infrastructure for ‘Trial within Cohorts’ study designs. BMC Cancer, 23(1), Article 648. https://doi.org/10.1186/s12885-023-11094-9
Yildirim, Hilin ; Widdershoven, Christiaan V. ; Aarts, Maureen Jb et al. / The PRO-RCC study : a long-term PROspective Renal Cell Carcinoma cohort in the Netherlands, providing an infrastructure for ‘Trial within Cohorts’ study designs. In: BMC Cancer. 2023 ; Vol. 23, No. 1.
@article{bf7777ade10a4962a799c5d0f2d56c18,
title = "The PRO-RCC study: a long-term PROspective Renal Cell Carcinoma cohort in the Netherlands, providing an infrastructure for {\textquoteleft}Trial within Cohorts{\textquoteright} study designs",
abstract = "Background: Ongoing research in the field of both localized, locally advanced and metastatic renal cell carcinoma has resulted in the availability of multiple treatment options. Hence, many questions are still unanswered and await further research. A nationwide collaborative registry allows to collect corresponding data. For this purpose, the Dutch PROspective Renal Cell Carcinoma cohort (PRO-RCC) has been founded, for the prospective collection of long-term clinical data, patient reported outcome measures (PROMs) and patient reported experience measures (PREMs). Methods: PRO-RCC is designed as a multicenter cohort for all Dutch patients with renal cell carcinoma (RCC). Recruitment will start in the Netherlands in 2023. Importantly, participants may also consent to participation in a {\textquoteleft}Trial within cohorts{\textquoteright} studies (TwiCs). The TwiCs design provides a method to perform (randomized) interventional studies within the registry. The clinical data collection is embedded in the Netherlands Cancer Registry (NCR). Next to the standardly available data on RCC, additional clinical data will be collected. PROMS entail Health-Related Quality of Life (HRQoL), symptom monitoring with optional ecological momentary assessment (EMA) of pain and fatigue, and optional return to work- and/or nutrition questionnaires. PREMS entail satisfaction with care. Both PROMS and PREMS are collected through the PROFILES registry and are accessible for the patient and the treating physician. Trial registration: Ethical board approval has been obtained (2021_218) and the study has been registered at ClinicalTrials.gov (NCT05326620). Discussion: PRO-RCC is a nationwide long-term cohort for the collection of real-world clinical data, PROMS and PREMS. By facilitating an infrastructure for the collection of prospective data on RCC, PRO-RCC will contribute to observational research in a real-world study population and prove effectiveness in daily clinical practice. The infrastructure of this cohort also enables that interventional studies can be conducted with the TwiCs design, without the disadvantages of classic RCTs such as slow patient accrual and risk of dropping out after randomization.",
author = "Hilin Yildirim and Widdershoven, {Christiaan V.} and Aarts, {Maureen Jb} and Axel Bex and Bloemendal, {Haiko J.} and Bochove-Overgaauw, {Deirdre M.} and Paul Hamberg and Herbschleb, {Karin H.} and {van der Hulle}, Tom and Lagerveld, {Brunolf W.} and {van Oijen}, {Martijn Gh} and Oosting, {Sjoukje F.} and {van Thienen}, {Johannes V.} and {van der Veldt}, {Astrid Am} and Westgeest, {Hans M.} and Zeijdner, {Evelijn E.} and Aben, {Katja Kh} and {van den Hurk}, Corina and Zondervan, {Patricia J.} and Bins, {Adriaan D.}",
note = "Funding Information: We would like to thank the Profiles Registry advisory board , the Dutch Federation of Cancer Patient Organizations (NFK), the Dutch patient association of bladder or kidney cancer (”Leven met Blaas- of Nierkanker”) for their contribution in the design of the cohort. We would like to thank the following experts on their contribution in the design of the cohort: Nutrition: Dr. A. Vrieling, Dr. S. Beijer. EMA: dr. B. de Rooij en prof. M. van der Lee for the EMA expertise. Cost-effectiveness: Dr. S. de Groot. Return to work: Prof. A. de Boer, Dr. S. Duijts. Funding: To date, PRO-RCC received funding for the set-up and maintenance of the infrastructure from MSD, Ipsen and Bristol Myers Squibb. The funding parties did not contribute to the study design or the manuscript. Award/grant number: N/A. Publisher Copyright: {\textcopyright} 2023, The Author(s).",
year = "2023",
month = jul,
day = "11",
doi = "10.1186/s12885-023-11094-9",
language = "English",
volume = "23",
journal = "BMC Cancer",
issn = "1471-2407",
publisher = "BioMed Central Ltd.",
number = "1",
}
Yildirim, H, Widdershoven, CV, Aarts, MJ, Bex, A, Bloemendal, HJ, Bochove-Overgaauw, DM, Hamberg, P, Herbschleb, KH, van der Hulle, T, Lagerveld, BW, van Oijen, MG, Oosting, SF, van Thienen, JV, van der Veldt, AA, Westgeest, HM, Zeijdner, EE, Aben, KK, van den Hurk, C, Zondervan, PJ & Bins, AD 2023, 'The PRO-RCC study: a long-term PROspective Renal Cell Carcinoma cohort in the Netherlands, providing an infrastructure for ‘Trial within Cohorts’ study designs', BMC Cancer, vol. 23, no. 1, 648. https://doi.org/10.1186/s12885-023-11094-9
The PRO-RCC study: a long-term PROspective Renal Cell Carcinoma cohort in the Netherlands, providing an infrastructure for ‘Trial within Cohorts’ study designs. / Yildirim, Hilin; Widdershoven, Christiaan V.; Aarts, Maureen Jb et al.
In: BMC Cancer, Vol. 23, No. 1, 648, 11.07.2023.
Research output: Contribution to journal › Article › Academic › peer-review
TY - JOUR
T1 - The PRO-RCC study
T2 - a long-term PROspective Renal Cell Carcinoma cohort in the Netherlands, providing an infrastructure for ‘Trial within Cohorts’ study designs
AU - Yildirim, Hilin
AU - Widdershoven, Christiaan V.
AU - Aarts, Maureen Jb
AU - Bex, Axel
AU - Bloemendal, Haiko J.
AU - Bochove-Overgaauw, Deirdre M.
AU - Hamberg, Paul
AU - Herbschleb, Karin H.
AU - van der Hulle, Tom
AU - Lagerveld, Brunolf W.
AU - van Oijen, Martijn Gh
AU - Oosting, Sjoukje F.
AU - van Thienen, Johannes V.
AU - van der Veldt, Astrid Am
AU - Westgeest, Hans M.
AU - Zeijdner, Evelijn E.
AU - Aben, Katja Kh
AU - van den Hurk, Corina
AU - Zondervan, Patricia J.
AU - Bins, Adriaan D.
N1 - Funding Information:We would like to thank the Profiles Registry advisory board , the Dutch Federation of Cancer Patient Organizations (NFK), the Dutch patient association of bladder or kidney cancer (”Leven met Blaas- of Nierkanker”) for their contribution in the design of the cohort. We would like to thank the following experts on their contribution in the design of the cohort: Nutrition: Dr. A. Vrieling, Dr. S. Beijer. EMA: dr. B. de Rooij en prof. M. van der Lee for the EMA expertise. Cost-effectiveness: Dr. S. de Groot. Return to work: Prof. A. de Boer, Dr. S. Duijts.Funding:To date, PRO-RCC received funding for the set-up and maintenance of theinfrastructure from MSD, Ipsen and Bristol Myers Squibb. The funding partiesdid not contribute to the study design or the manuscript.Award/grant number: N/A.Publisher Copyright:© 2023, The Author(s).
PY - 2023/7/11
Y1 - 2023/7/11
N2 - Background: Ongoing research in the field of both localized, locally advanced and metastatic renal cell carcinoma has resulted in the availability of multiple treatment options. Hence, many questions are still unanswered and await further research. A nationwide collaborative registry allows to collect corresponding data. For this purpose, the Dutch PROspective Renal Cell Carcinoma cohort (PRO-RCC) has been founded, for the prospective collection of long-term clinical data, patient reported outcome measures (PROMs) and patient reported experience measures (PREMs). Methods: PRO-RCC is designed as a multicenter cohort for all Dutch patients with renal cell carcinoma (RCC). Recruitment will start in the Netherlands in 2023. Importantly, participants may also consent to participation in a ‘Trial within cohorts’ studies (TwiCs). The TwiCs design provides a method to perform (randomized) interventional studies within the registry. The clinical data collection is embedded in the Netherlands Cancer Registry (NCR). Next to the standardly available data on RCC, additional clinical data will be collected. PROMS entail Health-Related Quality of Life (HRQoL), symptom monitoring with optional ecological momentary assessment (EMA) of pain and fatigue, and optional return to work- and/or nutrition questionnaires. PREMS entail satisfaction with care. Both PROMS and PREMS are collected through the PROFILES registry and are accessible for the patient and the treating physician. Trial registration: Ethical board approval has been obtained (2021_218) and the study has been registered at ClinicalTrials.gov (NCT05326620). Discussion: PRO-RCC is a nationwide long-term cohort for the collection of real-world clinical data, PROMS and PREMS. By facilitating an infrastructure for the collection of prospective data on RCC, PRO-RCC will contribute to observational research in a real-world study population and prove effectiveness in daily clinical practice. The infrastructure of this cohort also enables that interventional studies can be conducted with the TwiCs design, without the disadvantages of classic RCTs such as slow patient accrual and risk of dropping out after randomization.
AB - Background: Ongoing research in the field of both localized, locally advanced and metastatic renal cell carcinoma has resulted in the availability of multiple treatment options. Hence, many questions are still unanswered and await further research. A nationwide collaborative registry allows to collect corresponding data. For this purpose, the Dutch PROspective Renal Cell Carcinoma cohort (PRO-RCC) has been founded, for the prospective collection of long-term clinical data, patient reported outcome measures (PROMs) and patient reported experience measures (PREMs). Methods: PRO-RCC is designed as a multicenter cohort for all Dutch patients with renal cell carcinoma (RCC). Recruitment will start in the Netherlands in 2023. Importantly, participants may also consent to participation in a ‘Trial within cohorts’ studies (TwiCs). The TwiCs design provides a method to perform (randomized) interventional studies within the registry. The clinical data collection is embedded in the Netherlands Cancer Registry (NCR). Next to the standardly available data on RCC, additional clinical data will be collected. PROMS entail Health-Related Quality of Life (HRQoL), symptom monitoring with optional ecological momentary assessment (EMA) of pain and fatigue, and optional return to work- and/or nutrition questionnaires. PREMS entail satisfaction with care. Both PROMS and PREMS are collected through the PROFILES registry and are accessible for the patient and the treating physician. Trial registration: Ethical board approval has been obtained (2021_218) and the study has been registered at ClinicalTrials.gov (NCT05326620). Discussion: PRO-RCC is a nationwide long-term cohort for the collection of real-world clinical data, PROMS and PREMS. By facilitating an infrastructure for the collection of prospective data on RCC, PRO-RCC will contribute to observational research in a real-world study population and prove effectiveness in daily clinical practice. The infrastructure of this cohort also enables that interventional studies can be conducted with the TwiCs design, without the disadvantages of classic RCTs such as slow patient accrual and risk of dropping out after randomization.
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U2 - 10.1186/s12885-023-11094-9
DO - 10.1186/s12885-023-11094-9
M3 - Article
C2 - 37434119
AN - SCOPUS:85164409590
SN - 1471-2407
VL - 23
JO - BMC Cancer
JF - BMC Cancer
IS - 1
M1 - 648
ER -
Yildirim H, Widdershoven CV, Aarts MJ, Bex A, Bloemendal HJ, Bochove-Overgaauw DM et al. The PRO-RCC study: a long-term PROspective Renal Cell Carcinoma cohort in the Netherlands, providing an infrastructure for ‘Trial within Cohorts’ study designs. BMC Cancer. 2023 Jul 11;23(1):648. doi: 10.1186/s12885-023-11094-9