Importance of androgen-deprivation therapy during enzalutamide treatment in men with metastatic castration-resistant prostate cancer following chemotherapy: results from retrospective, multicenter ... View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-03

AUTHORS

Chang Wook Jeong, Minyong Kang, Seung Il Jung, Tae-Hwan Kim, Sung Woo Park, Jae Young Joung, Seong Soo Jeon, Jun Hyuk Hong, Ji Youl Lee, Byung Ha Chung, Hanjong Ahn, Choung-Soo Kim, Dong Deuk Kwon, Cheol Kwak

ABSTRACT

BACKGROUND: Enzalutamide can significantly prolong the survival of patients with metastatic castration-resistant prostate cancer (mCRPC). However, there is a paucity of evidence on continuing androgen-deprivation therapy (ADT) for mCRPC. Here, we analyzed the effect of concomitant ADT during enzalutamide treatment in men with mCRPC following chemotherapy. METHODS: We retrospectively reviewed the medical records of 232 patients with mCRPC who received oral enzalutamide (160 mg per day) following chemotherapy at 9 tertiary centers in Korea between 2014 and 2016. The primary endpoint was overall survival, while secondary endpoints included time to prostate-specific antigen (PSA) progression and radiographic progression-free survival. RESULTS: The median age of the patients was 71 years (interquartile range, 64-75 years). The proportion of patients in a grade group ≥4 was 77.6%. The rate of concomitant ADT was 29.3%, and the all-cause mortality rate was 27.1% (n = 63). Median overall survival, time to PSA progression, and radiographic progression-free survival were 24.0, 8.0, and 10.0 months, respectively. Notably, concomitant ADT showed a significant association with longer overall survival (median duration not reached vs. 18.2 months; p = 0.008). After adjusting for confounding factors, concomitant ADT was still associated with longer overall survival (hazard ratio, 0.35; 95% confidence interval, 0.17-0.72). CONCLUSION: Concomitant ADT during enzalutamide treatment may improve the survival of patients with mCRPC following chemotherapy. More... »

PAGES

150-158

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41391-018-0088-z

DOI

http://dx.doi.org/10.1038/s41391-018-0088-z

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1106945780

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30214035


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Download the RDF metadata as:  json-ld nt turtle xml License info

HOW TO GET THIS DATA PROGRAMMATICALLY:

JSON-LD is a popular format for linked data which is fully compatible with JSON.

curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1038/s41391-018-0088-z'

N-Triples is a line-based linked data format ideal for batch operations.

curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1038/s41391-018-0088-z'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1038/s41391-018-0088-z'

RDF/XML is a standard XML format for linked data.

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1038/s41391-018-0088-z'


 

This table displays all metadata directly associated to this object as RDF triples.

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312 schema:name Center for Prostate Cancer, National Cancer Center, Goyang, South Korea
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314 https://www.grid.ac/institutes/grid.411602.0 schema:alternateName Chonnam National University Hwasun Hospital
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318 schema:name Department of Urology, St. Mary Hospital, Catholic University College of Medicine, Seoul, South Korea
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320 https://www.grid.ac/institutes/grid.412591.a schema:alternateName Pusan National University Yangsan Hospital
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323 https://www.grid.ac/institutes/grid.413967.e schema:alternateName Asan Medical Center
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