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Prognostic Association between Common Laboratory Tests and Overall Survival in Elderly Men with De Novo Metastatic Castration Sensitive Prostate Cancer: A Population-Based Study in Canada Wallis, Christopher J. D.; Shayegan, Bobby; Morgan, Scott C.; Hamilton, Robert J.; Cagiannos, Ilias; Basappa, Naveen S.; Ferrario, Cristiano; Gotto, Geoffrey T.; Fernandes, Ricardo; Roy, Soumyajit; Noonan, Krista; Niazi, Tamim; Hotte, Sebastien J.; Saad, Fred; Hew, Huong; Chan, Katherine F. Y.; Park-Wyllie, Laura; Malone, Shawn
Abstract
De novo cases of metastatic prostate cancer (mCSPC) are associated with poorer prognosis. To assist in clinical decision-making, we aimed to determine the prognostic utility of commonly available laboratory-based markers with overall survival (OS). In a retrospective population-based study, a cohort of 3556 men aged ≥66 years diagnosed with de novo mCSPC between 2014 and 2019 was identified in Ontario (Canada) administrative database. OS was assessed by using the Kaplan–Meier method. Multivariate Cox regression analysis was performed to evaluate the association between laboratory markers and OS adjusting for patient and disease characteristics. Laboratory markers that were assessed include neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), albumin, hemoglobin, serum testosterone and PSA kinetics. Among the 3556 older men with de novo mCSPC, their median age was 77 years (IQR: 71–83). The median survival was 18 months (IQR: 10–31). In multivariate analysis, a statistically significant association with OS was observed with all the markers (NLR, PLR, albumin, hemoglobin, PSA decrease, reaching PSA nadir and a 50% PSA decline), except for testosterone levels. Our findings support the use of markers of systemic inflammation (NLR, PLR and albumin), hemoglobin and PSA metrics as prognostic indicators for OS in de novo mCSPC.
Item Metadata
| Title |
Prognostic Association between Common Laboratory Tests and Overall Survival in Elderly Men with De Novo Metastatic Castration Sensitive Prostate Cancer: A Population-Based Study in Canada
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| Creator |
Wallis, Christopher J. D.; Shayegan, Bobby; Morgan, Scott C.; Hamilton, Robert J.; Cagiannos, Ilias; Basappa, Naveen S.; Ferrario, Cristiano; Gotto, Geoffrey T.; Fernandes, Ricardo; Roy, Soumyajit; Noonan, Krista; Niazi, Tamim; Hotte, Sebastien J.; Saad, Fred; Hew, Huong; Chan, Katherine F. Y.; Park-Wyllie, Laura; Malone, Shawn
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| Contributor | |
| Publisher |
Multidisciplinary Digital Publishing Institute
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| Date Issued |
2021-06-07
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| Description |
De novo cases of metastatic prostate cancer (mCSPC) are associated with poorer prognosis. To assist in clinical decision-making, we aimed to determine the prognostic utility of commonly available laboratory-based markers with overall survival (OS). In a retrospective population-based study, a cohort of 3556 men aged ≥66 years diagnosed with de novo mCSPC between 2014 and 2019 was identified in Ontario (Canada) administrative database. OS was assessed by using the Kaplan–Meier method. Multivariate Cox regression analysis was performed to evaluate the association between laboratory markers and OS adjusting for patient and disease characteristics. Laboratory markers that were assessed include neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), albumin, hemoglobin, serum testosterone and PSA kinetics. Among the 3556 older men with de novo mCSPC, their median age was 77 years (IQR: 71–83). The median survival was 18 months (IQR: 10–31). In multivariate analysis, a statistically significant association with OS was observed with all the markers (NLR, PLR, albumin, hemoglobin, PSA decrease, reaching PSA nadir and a 50% PSA decline), except for testosterone levels. Our findings support the use of markers of systemic inflammation (NLR, PLR and albumin), hemoglobin and PSA metrics as prognostic indicators for OS in de novo mCSPC.
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| Subject | |
| Genre | |
| Type | |
| Language |
eng
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| Date Available |
2021-06-17
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| Provider |
Vancouver : University of British Columbia Library
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| Rights |
CC BY 4.0
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| DOI |
10.14288/1.0398447
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| URI | |
| Affiliation | |
| Citation |
Cancers 13 (11): 2844 (2021)
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| Publisher DOI |
10.3390/cancers13112844
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| Peer Review Status |
Reviewed
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| Scholarly Level |
Faculty; Researcher
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| Rights URI | |
| Aggregated Source Repository |
DSpace
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Item Citations and Data
Rights
CC BY 4.0