Cargando…

Incidence of central nervous system metastases in patients with HER2-positive metastatic breast cancer treated with pertuzumab, trastuzumab, and docetaxel: results from the randomized phase III study CLEOPATRA

BACKGROUND: Results from the phase III trial CLEOPATRA in human epidermal growth factor receptor 2-positive first-line metastatic breast cancer demonstrated significant improvements in progression-free and overall survival with pertuzumab, trastuzumab, and docetaxel over placebo, trastuzumab, and do...

Descripción completa

Detalles Bibliográficos
Autores principales: Swain, S. M., Baselga, J., Miles, D., Im, Y.-H., Quah, C., Lee, L. F., Cortés, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037862/
https://www.ncbi.nlm.nih.gov/pubmed/24685829
http://dx.doi.org/10.1093/annonc/mdu133
_version_ 1782318294528688128
author Swain, S. M.
Baselga, J.
Miles, D.
Im, Y.-H.
Quah, C.
Lee, L. F.
Cortés, J.
author_facet Swain, S. M.
Baselga, J.
Miles, D.
Im, Y.-H.
Quah, C.
Lee, L. F.
Cortés, J.
author_sort Swain, S. M.
collection PubMed
description BACKGROUND: Results from the phase III trial CLEOPATRA in human epidermal growth factor receptor 2-positive first-line metastatic breast cancer demonstrated significant improvements in progression-free and overall survival with pertuzumab, trastuzumab, and docetaxel over placebo, trastuzumab, and docetaxel. We carried out exploratory analyses of the incidence and time to development of central nervous system (CNS) metastases in patients from CLEOPATRA. PATIENTS AND METHODS: Patients received pertuzumab/placebo: 840 mg in cycle 1, then 420 mg; trastuzumab: 8 mg/kg in cycle 1, then 6 mg/kg; docetaxel: initiated at 75 mg/m(2). Study drugs were administered i.v. every 3 weeks. The log-rank test was used for between-arm comparisons of time to CNS metastases as first site of disease progression and overall survival in patients with CNS metastases as first site of disease progression. The Kaplan–Meier approach was used to estimate median time to CNS metastases as first site of disease progression and median overall survival. RESULTS: The incidence of CNS metastases as first site of disease progression was similar between arms; placebo arm: 51 of 406 (12.6%), pertuzumab arm: 55 of 402 (13.7%). Median time to development of CNS metastases as first site of disease progression was 11.9 months in the placebo arm and 15.0 months in the pertuzumab arm; hazard ratio (HR) = 0.58, 95% confidence interval (CI) 0.39–0.85, P = 0.0049. Overall survival in patients who developed CNS metastases as first site of disease progression showed a trend in favor of pertuzumab, trastuzumab, and docetaxel; HR = 0.66, 95% CI 0.39–1.11. Median overall survival was 26.3 versus 34.4 months in the placebo and pertuzumab arms, respectively. Treatment comparison of the survival curves was not statistically significant for the log-rank test (P = 0.1139), but significant for the Wilcoxon test (P = 0.0449). CONCLUSIONS: While the incidence of CNS metastases was similar between arms, our results suggest that pertuzumab, trastuzumab, and docetaxel delays the onset of CNS disease compared with placebo, trastuzumab, and docetaxel. CLINICALTRIALS.GOV: NCT00567190.
format Online
Article
Text
id pubmed-4037862
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-40378622014-05-29 Incidence of central nervous system metastases in patients with HER2-positive metastatic breast cancer treated with pertuzumab, trastuzumab, and docetaxel: results from the randomized phase III study CLEOPATRA Swain, S. M. Baselga, J. Miles, D. Im, Y.-H. Quah, C. Lee, L. F. Cortés, J. Ann Oncol Original Articles BACKGROUND: Results from the phase III trial CLEOPATRA in human epidermal growth factor receptor 2-positive first-line metastatic breast cancer demonstrated significant improvements in progression-free and overall survival with pertuzumab, trastuzumab, and docetaxel over placebo, trastuzumab, and docetaxel. We carried out exploratory analyses of the incidence and time to development of central nervous system (CNS) metastases in patients from CLEOPATRA. PATIENTS AND METHODS: Patients received pertuzumab/placebo: 840 mg in cycle 1, then 420 mg; trastuzumab: 8 mg/kg in cycle 1, then 6 mg/kg; docetaxel: initiated at 75 mg/m(2). Study drugs were administered i.v. every 3 weeks. The log-rank test was used for between-arm comparisons of time to CNS metastases as first site of disease progression and overall survival in patients with CNS metastases as first site of disease progression. The Kaplan–Meier approach was used to estimate median time to CNS metastases as first site of disease progression and median overall survival. RESULTS: The incidence of CNS metastases as first site of disease progression was similar between arms; placebo arm: 51 of 406 (12.6%), pertuzumab arm: 55 of 402 (13.7%). Median time to development of CNS metastases as first site of disease progression was 11.9 months in the placebo arm and 15.0 months in the pertuzumab arm; hazard ratio (HR) = 0.58, 95% confidence interval (CI) 0.39–0.85, P = 0.0049. Overall survival in patients who developed CNS metastases as first site of disease progression showed a trend in favor of pertuzumab, trastuzumab, and docetaxel; HR = 0.66, 95% CI 0.39–1.11. Median overall survival was 26.3 versus 34.4 months in the placebo and pertuzumab arms, respectively. Treatment comparison of the survival curves was not statistically significant for the log-rank test (P = 0.1139), but significant for the Wilcoxon test (P = 0.0449). CONCLUSIONS: While the incidence of CNS metastases was similar between arms, our results suggest that pertuzumab, trastuzumab, and docetaxel delays the onset of CNS disease compared with placebo, trastuzumab, and docetaxel. CLINICALTRIALS.GOV: NCT00567190. Oxford University Press 2014-06 2014-03-31 /pmc/articles/PMC4037862/ /pubmed/24685829 http://dx.doi.org/10.1093/annonc/mdu133 Text en © The Author 2014. Published by Oxford University Press on behalf of the European Society for Medical Oncology. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Swain, S. M.
Baselga, J.
Miles, D.
Im, Y.-H.
Quah, C.
Lee, L. F.
Cortés, J.
Incidence of central nervous system metastases in patients with HER2-positive metastatic breast cancer treated with pertuzumab, trastuzumab, and docetaxel: results from the randomized phase III study CLEOPATRA
title Incidence of central nervous system metastases in patients with HER2-positive metastatic breast cancer treated with pertuzumab, trastuzumab, and docetaxel: results from the randomized phase III study CLEOPATRA
title_full Incidence of central nervous system metastases in patients with HER2-positive metastatic breast cancer treated with pertuzumab, trastuzumab, and docetaxel: results from the randomized phase III study CLEOPATRA
title_fullStr Incidence of central nervous system metastases in patients with HER2-positive metastatic breast cancer treated with pertuzumab, trastuzumab, and docetaxel: results from the randomized phase III study CLEOPATRA
title_full_unstemmed Incidence of central nervous system metastases in patients with HER2-positive metastatic breast cancer treated with pertuzumab, trastuzumab, and docetaxel: results from the randomized phase III study CLEOPATRA
title_short Incidence of central nervous system metastases in patients with HER2-positive metastatic breast cancer treated with pertuzumab, trastuzumab, and docetaxel: results from the randomized phase III study CLEOPATRA
title_sort incidence of central nervous system metastases in patients with her2-positive metastatic breast cancer treated with pertuzumab, trastuzumab, and docetaxel: results from the randomized phase iii study cleopatra
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037862/
https://www.ncbi.nlm.nih.gov/pubmed/24685829
http://dx.doi.org/10.1093/annonc/mdu133
work_keys_str_mv AT swainsm incidenceofcentralnervoussystemmetastasesinpatientswithher2positivemetastaticbreastcancertreatedwithpertuzumabtrastuzumabanddocetaxelresultsfromtherandomizedphaseiiistudycleopatra
AT baselgaj incidenceofcentralnervoussystemmetastasesinpatientswithher2positivemetastaticbreastcancertreatedwithpertuzumabtrastuzumabanddocetaxelresultsfromtherandomizedphaseiiistudycleopatra
AT milesd incidenceofcentralnervoussystemmetastasesinpatientswithher2positivemetastaticbreastcancertreatedwithpertuzumabtrastuzumabanddocetaxelresultsfromtherandomizedphaseiiistudycleopatra
AT imyh incidenceofcentralnervoussystemmetastasesinpatientswithher2positivemetastaticbreastcancertreatedwithpertuzumabtrastuzumabanddocetaxelresultsfromtherandomizedphaseiiistudycleopatra
AT quahc incidenceofcentralnervoussystemmetastasesinpatientswithher2positivemetastaticbreastcancertreatedwithpertuzumabtrastuzumabanddocetaxelresultsfromtherandomizedphaseiiistudycleopatra
AT leelf incidenceofcentralnervoussystemmetastasesinpatientswithher2positivemetastaticbreastcancertreatedwithpertuzumabtrastuzumabanddocetaxelresultsfromtherandomizedphaseiiistudycleopatra
AT cortesj incidenceofcentralnervoussystemmetastasesinpatientswithher2positivemetastaticbreastcancertreatedwithpertuzumabtrastuzumabanddocetaxelresultsfromtherandomizedphaseiiistudycleopatra