CARD-Studie – Bedeutung für die Therapie des fortgeschrittenen Prostatakarzinoms

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CARD-Studie – Bedeutung für die Therapie des fortgeschrittenen Prostatakarzinoms. / Merseburger, Axel S; Bannowsky, Andreas; Becker, Klaus; Bokemeyer, Carsten; Eichenauer, Rolf; Lehmann, Jan; Mickisch, Gerald; Steuber, Thomas; von Amsberg, Gunhild; von Kügelgen, Tobias; Wülfing, Christian.

In: AKTUEL UROL, Vol. 2020, 2020.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Merseburger, AS, Bannowsky, A, Becker, K, Bokemeyer, C, Eichenauer, R, Lehmann, J, Mickisch, G, Steuber, T, von Amsberg, G, von Kügelgen, T & Wülfing, C 2020, 'CARD-Studie – Bedeutung für die Therapie des fortgeschrittenen Prostatakarzinoms', AKTUEL UROL, vol. 2020. https://doi.org/10.1055/a-1247-4155

APA

Merseburger, A. S., Bannowsky, A., Becker, K., Bokemeyer, C., Eichenauer, R., Lehmann, J., Mickisch, G., Steuber, T., von Amsberg, G., von Kügelgen, T., & Wülfing, C. (2020). CARD-Studie – Bedeutung für die Therapie des fortgeschrittenen Prostatakarzinoms. AKTUEL UROL, 2020. https://doi.org/10.1055/a-1247-4155

Vancouver

Bibtex

@article{ad6ac4f24bbe475d8b317955f3656831,
title = "CARD-Studie – Bedeutung f{\"u}r die Therapie des fortgeschrittenen Prostatakarzinoms",
abstract = "BACKGROUND:  Various life-prolonging therapy options are available for the treatment of metastatic castration-resistant prostate cancer (mCRPC).OBJECTIVE:  The optimal therapy sequence for mCRPC has been discussed for years. With the final results of the CARD study, important prospective data are available to enlighten the discussion about the therapy sequence.MATERIAL AND METHOD:  CARD is a randomised phase IV trial in patients with mCRPC who were previously treated with docetaxel and an anti-androgen receptor (ARTA). The study showed significant efficacy benefits in favour of further treatment with cabazitaxel versus a second ARTA therapy. The study results are presented and discussed in the context of previous study data with regard to their importance for everyday clinical practice.RESULTS:  The CARD study data confirm cabazitaxel as an effective therapy option for mCRPC patients previously treated with docetaxel and an ARTA. Cabazitaxel was safe to apply. The study results confirm the cross resistance between the two ARTAs Abiraterone and Enzalutamide.CONCLUSION: In mCRPC patients eligible for chemotherapy, the therapy sequence should be chosen so that the patients also receive cabazitaxel. A direct therapy sequence with two ARTAs should be avoided or, at least, only considered if other substances are contraindicated.",
author = "Merseburger, {Axel S} and Andreas Bannowsky and Klaus Becker and Carsten Bokemeyer and Rolf Eichenauer and Jan Lehmann and Gerald Mickisch and Thomas Steuber and {von Amsberg}, Gunhild and {von K{\"u}gelgen}, Tobias and Christian W{\"u}lfing",
note = "Thieme. All rights reserved.",
year = "2020",
doi = "10.1055/a-1247-4155",
language = "Deutsch",
volume = "2020",
journal = "AKTUEL UROL",
issn = "0001-7868",
publisher = "Georg Thieme Verlag KG",

}

RIS

TY - JOUR

T1 - CARD-Studie – Bedeutung für die Therapie des fortgeschrittenen Prostatakarzinoms

AU - Merseburger, Axel S

AU - Bannowsky, Andreas

AU - Becker, Klaus

AU - Bokemeyer, Carsten

AU - Eichenauer, Rolf

AU - Lehmann, Jan

AU - Mickisch, Gerald

AU - Steuber, Thomas

AU - von Amsberg, Gunhild

AU - von Kügelgen, Tobias

AU - Wülfing, Christian

N1 - Thieme. All rights reserved.

PY - 2020

Y1 - 2020

N2 - BACKGROUND:  Various life-prolonging therapy options are available for the treatment of metastatic castration-resistant prostate cancer (mCRPC).OBJECTIVE:  The optimal therapy sequence for mCRPC has been discussed for years. With the final results of the CARD study, important prospective data are available to enlighten the discussion about the therapy sequence.MATERIAL AND METHOD:  CARD is a randomised phase IV trial in patients with mCRPC who were previously treated with docetaxel and an anti-androgen receptor (ARTA). The study showed significant efficacy benefits in favour of further treatment with cabazitaxel versus a second ARTA therapy. The study results are presented and discussed in the context of previous study data with regard to their importance for everyday clinical practice.RESULTS:  The CARD study data confirm cabazitaxel as an effective therapy option for mCRPC patients previously treated with docetaxel and an ARTA. Cabazitaxel was safe to apply. The study results confirm the cross resistance between the two ARTAs Abiraterone and Enzalutamide.CONCLUSION: In mCRPC patients eligible for chemotherapy, the therapy sequence should be chosen so that the patients also receive cabazitaxel. A direct therapy sequence with two ARTAs should be avoided or, at least, only considered if other substances are contraindicated.

AB - BACKGROUND:  Various life-prolonging therapy options are available for the treatment of metastatic castration-resistant prostate cancer (mCRPC).OBJECTIVE:  The optimal therapy sequence for mCRPC has been discussed for years. With the final results of the CARD study, important prospective data are available to enlighten the discussion about the therapy sequence.MATERIAL AND METHOD:  CARD is a randomised phase IV trial in patients with mCRPC who were previously treated with docetaxel and an anti-androgen receptor (ARTA). The study showed significant efficacy benefits in favour of further treatment with cabazitaxel versus a second ARTA therapy. The study results are presented and discussed in the context of previous study data with regard to their importance for everyday clinical practice.RESULTS:  The CARD study data confirm cabazitaxel as an effective therapy option for mCRPC patients previously treated with docetaxel and an ARTA. Cabazitaxel was safe to apply. The study results confirm the cross resistance between the two ARTAs Abiraterone and Enzalutamide.CONCLUSION: In mCRPC patients eligible for chemotherapy, the therapy sequence should be chosen so that the patients also receive cabazitaxel. A direct therapy sequence with two ARTAs should be avoided or, at least, only considered if other substances are contraindicated.

U2 - 10.1055/a-1247-4155

DO - 10.1055/a-1247-4155

M3 - SCORING: Zeitschriftenaufsatz

C2 - 32968994

VL - 2020

JO - AKTUEL UROL

JF - AKTUEL UROL

SN - 0001-7868

ER -