Natural History of Rising Serum Prostate-Specific Antigen in Men With Castrate Nonmetastatic Prostate Cancer

To describe the natural history of nonmetastatic prostate cancer and rising prostate-specific antigen (PSA) despite androgen deprivation therapy. The 201 patients in this report were the placebo control group from an aborted randomized controlled trial to evaluate the effects of zoledronic acid on t...

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Published inJournal of clinical oncology Vol. 23; no. 13; pp. 2918 - 2925
Main Authors SMITH, Matthew R, KABBINAVAR, Fairooz, LINNARTZ, Ronald, MING ZHENG, GOESSL, Carsten, HEI, Yong-Jiang, SMALL, Eric J, COOK, Richard, HIGANO, Celestia S, SAAD, Fred, ARIFHUSSAIN, GITTELMAN, Marc C, BILHARTZ, David L, WYNNE, Chris, MURRAY, Robin, ZINNER, Norman R, SCHULMAN, Claude
Format Journal Article
LanguageEnglish
Published Baltimore, MD American Society of Clinical Oncology 01.05.2005
Lippincott Williams & Wilkins
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Abstract To describe the natural history of nonmetastatic prostate cancer and rising prostate-specific antigen (PSA) despite androgen deprivation therapy. The 201 patients in this report were the placebo control group from an aborted randomized controlled trial to evaluate the effects of zoledronic acid on time to first bone metastasis in men with prostate cancer, no bone metastases, and rising PSA despite androgen deprivation therapy. Relationships between baseline covariates and clinical outcomes were assessed by Cox proportional hazard analyses. Covariates in the model were baseline PSA, Gleason sum, history of bilateral orchiectomies, regional lymph node metastases at diagnosis, prior prostatectomy, time from androgen deprivation therapy to random assignment, time from diagnosis to random assignment, and PSA velocity. At 2 years, 33% of patients had developed bone metastases. Median bone metastasis-free survival was 30 months. Median time to first bone metastases and overall survival were not reached. Baseline PSA level greater than 10 ng/mL (relative risk, 3.18; 95% CI, 1.74 to 5.80; P < .001) and PSA velocity (4.34 for each 0.01 increase in PSA velocity; 95% CI, 2.30 to 8.21; P < .001) independently predicted shorter time to first bone metastasis. Baseline PSA and PSA velocity also independently predicted overall survival and metastasis-free survival. Other covariates did not consistently predict clinical outcomes. Men with nonmetastatic prostate cancer and rising PSA despite androgen deprivation therapy have a relatively indolent natural history. Baseline PSA and PSA velocity independently predict time to first bone metastasis and survival.
AbstractList PURPOSETo describe the natural history of nonmetastatic prostate cancer and rising prostate-specific antigen (PSA) despite androgen deprivation therapy.PATIENTS AND METHODSThe 201 patients in this report were the placebo control group from an aborted randomized controlled trial to evaluate the effects of zoledronic acid on time to first bone metastasis in men with prostate cancer, no bone metastases, and rising PSA despite androgen deprivation therapy. Relationships between baseline covariates and clinical outcomes were assessed by Cox proportional hazard analyses. Covariates in the model were baseline PSA, Gleason sum, history of bilateral orchiectomies, regional lymph node metastases at diagnosis, prior prostatectomy, time from androgen deprivation therapy to random assignment, time from diagnosis to random assignment, and PSA velocity.RESULTSAt 2 years, 33% of patients had developed bone metastases. Median bone metastasis-free survival was 30 months. Median time to first bone metastases and overall survival were not reached. Baseline PSA level greater than 10 ng/mL (relative risk, 3.18; 95% CI, 1.74 to 5.80; P < .001) and PSA velocity (4.34 for each 0.01 increase in PSA velocity; 95% CI, 2.30 to 8.21; P < .001) independently predicted shorter time to first bone metastasis. Baseline PSA and PSA velocity also independently predicted overall survival and metastasis-free survival. Other covariates did not consistently predict clinical outcomes.CONCLUSIONMen with nonmetastatic prostate cancer and rising PSA despite androgen deprivation therapy have a relatively indolent natural history. Baseline PSA and PSA velocity independently predict time to first bone metastasis and survival.
To describe the natural history of nonmetastatic prostate cancer and rising prostate-specific antigen (PSA) despite androgen deprivation therapy. The 201 patients in this report were the placebo control group from an aborted randomized controlled trial to evaluate the effects of zoledronic acid on time to first bone metastasis in men with prostate cancer, no bone metastases, and rising PSA despite androgen deprivation therapy. Relationships between baseline covariates and clinical outcomes were assessed by Cox proportional hazard analyses. Covariates in the model were baseline PSA, Gleason sum, history of bilateral orchiectomies, regional lymph node metastases at diagnosis, prior prostatectomy, time from androgen deprivation therapy to random assignment, time from diagnosis to random assignment, and PSA velocity. At 2 years, 33% of patients had developed bone metastases. Median bone metastasis-free survival was 30 months. Median time to first bone metastases and overall survival were not reached. Baseline PSA level greater than 10 ng/mL (relative risk, 3.18; 95% CI, 1.74 to 5.80; P < .001) and PSA velocity (4.34 for each 0.01 increase in PSA velocity; 95% CI, 2.30 to 8.21; P < .001) independently predicted shorter time to first bone metastasis. Baseline PSA and PSA velocity also independently predicted overall survival and metastasis-free survival. Other covariates did not consistently predict clinical outcomes. Men with nonmetastatic prostate cancer and rising PSA despite androgen deprivation therapy have a relatively indolent natural history. Baseline PSA and PSA velocity independently predict time to first bone metastasis and survival.
Purpose To describe the natural history of nonmetastatic prostate cancer and rising prostate-specific antigen (PSA) despite androgen deprivation therapy. Patients and Methods: The 201 patients in this report were the placebo control group from an aborted randomized controlled trial to evaluate the effects of zoledronic acid on time to first bone metastasis in men with prostate cancer, no bone metastases, and rising PSA despite androgen deprivation therapy. Relationships between baseline covariates and clinical outcomes were assessed by Cox proportional hazard analyses. Covariates in the model were baseline PSA, Gleason sum, history of bilateral orchiectomies, regional lymph node metastases at diagnosis, prior prostatectomy, time from androgen deprivation therapy to random assignment, time from diagnosis to random assignment, and PSA velocity. Results At 2 years, 33% of patients had developed bone metastases. Median bone metastasis–free survival was 30 months. Median time to first bone metastases and overall survival were not reached. Baseline PSA level greater than 10 ng/mL (relative risk, 3.18; 95% CI, 1.74 to 5.80; P < .001) and PSA velocity (4.34 for each 0.01 increase in PSA velocity; 95% CI, 2.30 to 8.21; P < .001) independently predicted shorter time to first bone metastasis. Baseline PSA and PSA velocity also independently predicted overall survival and metastasis-free survival. Other covariates did not consistently predict clinical outcomes. Conclusion Men with nonmetastatic prostate cancer and rising PSA despite androgen deprivation therapy have a relatively indolent natural history. Baseline PSA and PSA velocity independently predict time to first bone metastasis and survival.
Author Robin Murray
Fred Saad
Eric J. Small
Arif Hussain
Ronald Linnartz
Matthew R. Smith
Marc C. Gittelman
Ming Zheng
Norman R. Zinner
Chris Wynne
Yong-Jiang Hei
Celestia S. Higano
David L. Bilhartz
Richard Cook
Claude Schulman
Carsten Goessl
Fairooz Kabbinavar
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  organization: Christchurch Hospital, Christchurch, New Zealand
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  fullname: SCHULMAN, Claude
  organization: Christchurch Hospital, Christchurch, New Zealand
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Cites_doi 10.1200/JCO.2002.03.061
10.1056/NEJM199707313370502
10.1016/S0360-3016(97)00082-5
10.3322/canjclin.54.1.8
10.1093/jnci/djg043
10.1002/9781118032985
10.1002/(SICI)1097-0142(19981101)83:9<1989::AID-CNCR15>3.0.CO;2-V
10.1046/j.1464-410X.1997.d01-6840.x
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10.1200/JCO.1997.15.1.230
10.1016/S0360-3016(00)00717-3
10.1056/NEJMoa040720
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Issue 13
Keywords Prostate specific antigen
Human
Urinary system disease
Cancerology
Prostate disease
Adult
Serum
Tumoral marker
Malignant tumor
Male genital diseases
Prostate cancer
Language English
License CC BY 4.0
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PublicationTitle Journal of clinical oncology
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Lippincott Williams & Wilkins
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References 29686422 - Nat Rev Clin Oncol. 2018 Jun;15(6):350-351
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Snippet To describe the natural history of nonmetastatic prostate cancer and rising prostate-specific antigen (PSA) despite androgen deprivation therapy. The 201...
Purpose To describe the natural history of nonmetastatic prostate cancer and rising prostate-specific antigen (PSA) despite androgen deprivation therapy....
PURPOSETo describe the natural history of nonmetastatic prostate cancer and rising prostate-specific antigen (PSA) despite androgen deprivation...
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SubjectTerms Aged
Androgen Antagonists - therapeutic use
Biological and medical sciences
Biomarkers, Tumor - analysis
Bone Neoplasms - prevention & control
Bone Neoplasms - secondary
Diphosphonates - therapeutic use
Disease Progression
Double-Blind Method
Follow-Up Studies
Humans
Imidazoles - therapeutic use
Male
Medical sciences
Nephrology. Urinary tract diseases
Placebos
Predictive Value of Tests
Prognosis
Prostate-Specific Antigen - analysis
Prostatic Neoplasms - drug therapy
Prostatic Neoplasms - pathology
Survival Analysis
Tumors
Tumors of the urinary system
Urinary tract. Prostate gland
Zoledronic Acid
Title Natural History of Rising Serum Prostate-Specific Antigen in Men With Castrate Nonmetastatic Prostate Cancer
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