Efficacy and Safety of Cabazitaxel Versus Abiraterone or Enzalutamide in Older Patients with Metastatic Castration-resistant Prostate Cancer in the CARD Study
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články, randomizované kontrolované studie, práce podpořená grantem
PubMed
34274136
DOI
10.1016/j.eururo.2021.06.021
PII: S0302-2838(21)01862-5
Knihovny.cz E-zdroje
- Klíčová slova
- Cabazitaxel, Elderly, Metastatic castration-resistant prostate cancer, Prostate cancer,
- MeSH
- abirateron terapeutické užití MeSH
- androsteny MeSH
- benzamidy škodlivé účinky terapeutické užití MeSH
- docetaxel škodlivé účinky MeSH
- fenylthiohydantoin škodlivé účinky terapeutické užití MeSH
- lidé MeSH
- nádory prostaty rezistentní na kastraci * farmakoterapie MeSH
- nitrily škodlivé účinky terapeutické užití MeSH
- prednison škodlivé účinky MeSH
- přežití bez známek nemoci MeSH
- protokoly protinádorové kombinované chemoterapie škodlivé účinky MeSH
- senioři MeSH
- taxoidy škodlivé účinky terapeutické užití MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- abirateron MeSH
- abiraterone MeSH Prohlížeč
- androsteny MeSH
- benzamidy MeSH
- cabazitaxel MeSH Prohlížeč
- docetaxel MeSH
- enzalutamide MeSH Prohlížeč
- fenylthiohydantoin MeSH
- nitrily MeSH
- prednison MeSH
- taxoidy MeSH
BACKGROUND: In the CARD study (NCT02485691), cabazitaxel significantly improved median radiographic progression-free survival (rPFS) and overall survival (OS) versus abiraterone/enzalutamide in patients with metastatic castration-resistant prostate cancer (mCRPC) who had previously received docetaxel and progressed ≤12 mo on the alternative agent (abiraterone/enzalutamide). OBJECTIVE: To assess cabazitaxel versus abiraterone/enzalutamide in older (≥70 yr) and younger (<70 yr) patients in CARD. DESIGN, SETTING, AND PARTICIPANTS: Patients with mCRPC were randomized 1:1 to cabazitaxel (25 mg/m2 plus prednisone and granulocyte colony-stimulating factor) versus abiraterone (1000 mg plus prednisone) or enzalutamide (160 mg). OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Analyses of rPFS (primary endpoint) and safety by age were prespecified; others were post hoc. Treatment groups were compared using stratified log-rank or Cochran-Mantel-Haenszel tests. RESULTS AND LIMITATIONS: Of the 255 patients randomized, 135 were aged ≥70 yr (median 76 yr). Cabazitaxel, compared with abiraterone/enzalutamide, significantly improved median rPFS in older (8.2 vs 4.5 mo; hazard ratio [HR] = 0.58; 95% confidence interval [CI] = 0.38-0.89; p = 0.012) and younger (7.4 vs 3.2 mo; HR = 0.47; 95% CI = 0.30-0.74; p < 0.001) patients. The median OS of cabazitaxel versus abiraterone/enzalutamide was 13.9 versus 9.4 mo in older patients (HR = 0.66; 95% CI = 0.41-1.06; p = 0.084), and it was 13.6 versus 11.8 mo in younger patients (HR = 0.66; 95% CI = 0.41-1.08; p = 0.093). Progression-free survival, prostate-specific antigen, and tumor and pain responses favored cabazitaxel, regardless of age. Grade ≥3 treatment-emergent adverse events (TEAEs) occurred in 58% versus 49% of older patients receiving cabazitaxel versus abiraterone/enzalutamide and 48% versus 42% of younger patients. In older patients, cardiac adverse events were more frequent with abiraterone/enzalutamide; asthenia and diarrhea were more frequent with cabazitaxel. CONCLUSIONS: Cabazitaxel improved efficacy outcomes versus abiraterone/enzalutamide in patients with mCRPC after prior docetaxel and abiraterone/enzalutamide, regardless of age. TEAEs were more frequent among older patients. The cabazitaxel safety profile was manageable across age groups. PATIENT SUMMARY: Clinical trial data showed that cabazitaxel improved survival versus abiraterone/enzalutamide with manageable side effects in patients with metastatic castration-resistant prostate cancer who had previously received docetaxel and the alternative agent (abiraterone/enzalutamide), irrespective of age.
Alexandra Hospital National and Kapodistrian University of Athens Athens Greece
Department of Urology Asklepios Tumorzentrum Hamburg Asklepios Klinik Altona Hamburg Germany
Department of Urology Medical University of Vienna Vienna Austria
e Octubre University Hospital Madrid Spain
Erasmus University Hospital Rotterdam The Netherlands
Gustave Roussy Institute and University of Paris Saclay Villejuif France
Hôpital D'Instruction des Armées Bégin Saint Mandé France
Institute de Recherche Clinique Université Catholique de Louvain Brussels Belgium
Jean Godinot Institute Reims France
Landspitali University Hospital Reykjavik Iceland
Palacky University Medical School and Teaching Hospital Olomouc Czech Republic
Sanofi Europe Medical Oncology Paris France
Sanofi Global Medical Oncology Cambridge MA USA
Studienpraxis Urologie Nürtingen Germany
The Institute of Cancer Research and the Royal Marsden Hospital London UK
Vall d'Hebron Institute of Oncology Vall d'Hebron University Hospital Barcelona Spain
Citace poskytuje Crossref.org
ClinicalTrials.gov
NCT02485691