Meta-Analysis Evaluating the Impact of Site of Metastasis on Overall Survival in Men With Castration-Resistant Prostate Cancer.

dc.contributor.author

Halabi, Susan

dc.contributor.author

Kelly, William Kevin

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Ma, Hua

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Zhou, Haojin

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Solomon, Nicole C

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Fizazi, Karim

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Tangen, Catherine M

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Rosenthal, Mark

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Petrylak, Daniel P

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Hussain, Maha

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Vogelzang, Nicholas J

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Thompson, Ian M

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Chi, Kim N

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de Bono, Johann

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Armstrong, Andrew J

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Eisenberger, Mario A

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Fandi, Abderrahim

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Li, Shaoyi

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Araujo, John C

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Logothetis, Christopher J

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Quinn, David I

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Morris, Michael J

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Higano, Celestia S

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Tannock, Ian F

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Small, Eric J

dc.date.accessioned

2024-06-06T15:37:24Z

dc.date.available

2024-06-06T15:37:24Z

dc.date.issued

2016-05

dc.description.abstract

Purpose

Reports have suggested that metastatic site is an important predictor of overall survival (OS) in men with metastatic castration-resistant prostate cancer (mCRPC), but these were based on a limited number of patients. We investigate the impact of site of metastases on OS of a substantial sample of men with mCRPC who received docetaxel chemotherapy in nine phase III trials.

Patients and methods

Individual patient data from 8,820 men with mCRPC enrolled onto nine phase III trials were combined. Site of metastases was categorized as lymph node (LN) only, bone with or without LN (with no visceral metastases), any lung metastases (but no liver), and any liver metastases.

Results

Most patients had bone with or without LN metastases (72.8%), followed by visceral disease (20.8%) and LN-only disease (6.4%). Men with liver metastases had the worst median OS (13.5 months). Although men with lung metastases had better median OS (19.4 months) compared with men with liver metastases, they had significantly worse median survival duration than men with nonvisceral bone metastases (21.3 months). Men with LN-only disease had a median OS of 31.6 months. The pooled hazard ratios for death in men with lung metastases compared with men with bone with or without LN metastases and in men with any liver metastases compared with men with lung metastases were 1.14 (95% CI, 1.04 to 1.25; P = .007) and 1.52 (95% CI, 1.35 to 1.73; P < .0001), respectively.

Conclusion

Specific sites of metastases in men with mCRPC are associated with differential OS, with successive increased lethality for lung and liver metastases compared with bone and nonvisceral involvement. These data may help in treatment decisions, the design of future clinical trials, and understanding the variation in biology of different sites of metastases in men with mCRPC.
dc.identifier

JCO.2015.65.7270

dc.identifier.issn

0732-183X

dc.identifier.issn

1527-7755

dc.identifier.uri

https://hdl.handle.net/10161/31142

dc.language

eng

dc.publisher

American Society of Clinical Oncology (ASCO)

dc.relation.ispartof

Journal of clinical oncology : official journal of the American Society of Clinical Oncology

dc.relation.isversionof

10.1200/jco.2015.65.7270

dc.rights.uri

https://creativecommons.org/licenses/by-nc/4.0

dc.subject

Humans

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Bone Neoplasms

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Liver Neoplasms

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Lung Neoplasms

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Neoplasm Metastasis

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Aged

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Middle Aged

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Male

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Randomized Controlled Trials as Topic

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Clinical Trials, Phase III as Topic

dc.subject

Prostatic Neoplasms, Castration-Resistant

dc.title

Meta-Analysis Evaluating the Impact of Site of Metastasis on Overall Survival in Men With Castration-Resistant Prostate Cancer.

dc.type

Journal article

duke.contributor.orcid

Halabi, Susan|0000-0003-4135-2777

duke.contributor.orcid

Solomon, Nicole C|0000-0002-5643-9958

duke.contributor.orcid

Armstrong, Andrew J|0000-0001-7012-1754

pubs.begin-page

1652

pubs.end-page

1659

pubs.issue

14

pubs.organisational-group

Duke

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School of Medicine

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Staff

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Basic Science Departments

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Clinical Science Departments

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Institutes and Centers

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Biostatistics & Bioinformatics

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Pharmacology & Cancer Biology

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Medicine

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Medicine, Medical Oncology

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Duke Cancer Institute

pubs.organisational-group

Biostatistics & Bioinformatics, Division of Biostatistics

pubs.organisational-group

Urology

pubs.publication-status

Published

pubs.volume

34

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