Active surveillance for intermediate-risk prostate cancer in African American and non-Hispanic White men
© 2021 American Cancer Society..
BACKGROUND: The safety of active surveillance (AS) for African American men compared with non-Hispanic White (White) men with intermediate-risk prostate cancer is unclear.
METHODS: The authors identified patients with modified National Comprehensive Cancer Network favorable ("low-intermediate") and unfavorable ("high-intermediate") intermediate-risk prostate cancer diagnosed between 2001 and 2015 and initially managed with AS in the Veterans Health Administration database. They analyzed definitive treatment, disease progression, metastases, prostate cancer-specific mortality (PCSM), and all-cause mortality by using cumulative incidences and multivariable competing-risks (disease progression, metastasis, and PCSM) or Cox (all-cause mortality) regression.
RESULTS: The cohort included 1007 men (African Americans, 330 [32.8%]; Whites, 677 [67.2%]) followed for a median of 7.7 years; 773 (76.8%) had low-intermediate-risk disease, and 234 (23.2%) had high-intermediate-risk disease. The 10-year cumulative incidences of definitive treatment were not significantly different (African Americans, 83.5%; 95% confidence interval [CI], 78.5%-88.7%; Whites, 80.6%; 95% CI, 76.6%-84.4%; P = .17). Among those with low-intermediate-risk disease, there were no significant differences in the 10-year cumulative incidences of disease progression (African Americans, 46.8%; 95% CI, 40.0%-53.3%; Whites, 46.9%; 95% CI, 42.1%-51.5%; P = .91), metastasis (African Americans, 7.1%; 95% CI, 3.7%-11.8%; Whites, 10.8%; 95% CI, 7.6%-14.6%; P = .17), or PCSM (African Americans, 3.8%; 95% CI, 1.6%-7.5%; Whites, 3.8%; 95% CI, 2.0%-6.3%; P = .69). In a multivariable regression including the entire cohort, African American race was not associated with increased risks of definitive treatment, disease progression, metastasis, PCSM, or all-cause mortality (all P > .30).
CONCLUSIONS: Outcomes in the Veterans Affairs Health System were similar for African American and White men treated for low-intermediate-risk prostate cancer with AS.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2021 |
---|---|
Erschienen: |
2021 |
Enthalten in: |
Zur Gesamtaufnahme - volume:127 |
---|---|
Enthalten in: |
Cancer - 127(2021), 23 vom: 01. Dez., Seite 4403-4412 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Courtney, P Travis [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 09.03.2022 Date Revised 07.12.2022 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1002/cncr.33824 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM328917109 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM328917109 | ||
003 | DE-627 | ||
005 | 20231225203955.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2021 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1002/cncr.33824 |2 doi | |
028 | 5 | 2 | |a pubmed24n1096.xml |
035 | |a (DE-627)NLM328917109 | ||
035 | |a (NLM)34347291 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Courtney, P Travis |e verfasserin |4 aut | |
245 | 1 | 0 | |a Active surveillance for intermediate-risk prostate cancer in African American and non-Hispanic White men |
264 | 1 | |c 2021 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 09.03.2022 | ||
500 | |a Date Revised 07.12.2022 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2021 American Cancer Society. | ||
520 | |a BACKGROUND: The safety of active surveillance (AS) for African American men compared with non-Hispanic White (White) men with intermediate-risk prostate cancer is unclear | ||
520 | |a METHODS: The authors identified patients with modified National Comprehensive Cancer Network favorable ("low-intermediate") and unfavorable ("high-intermediate") intermediate-risk prostate cancer diagnosed between 2001 and 2015 and initially managed with AS in the Veterans Health Administration database. They analyzed definitive treatment, disease progression, metastases, prostate cancer-specific mortality (PCSM), and all-cause mortality by using cumulative incidences and multivariable competing-risks (disease progression, metastasis, and PCSM) or Cox (all-cause mortality) regression | ||
520 | |a RESULTS: The cohort included 1007 men (African Americans, 330 [32.8%]; Whites, 677 [67.2%]) followed for a median of 7.7 years; 773 (76.8%) had low-intermediate-risk disease, and 234 (23.2%) had high-intermediate-risk disease. The 10-year cumulative incidences of definitive treatment were not significantly different (African Americans, 83.5%; 95% confidence interval [CI], 78.5%-88.7%; Whites, 80.6%; 95% CI, 76.6%-84.4%; P = .17). Among those with low-intermediate-risk disease, there were no significant differences in the 10-year cumulative incidences of disease progression (African Americans, 46.8%; 95% CI, 40.0%-53.3%; Whites, 46.9%; 95% CI, 42.1%-51.5%; P = .91), metastasis (African Americans, 7.1%; 95% CI, 3.7%-11.8%; Whites, 10.8%; 95% CI, 7.6%-14.6%; P = .17), or PCSM (African Americans, 3.8%; 95% CI, 1.6%-7.5%; Whites, 3.8%; 95% CI, 2.0%-6.3%; P = .69). In a multivariable regression including the entire cohort, African American race was not associated with increased risks of definitive treatment, disease progression, metastasis, PCSM, or all-cause mortality (all P > .30) | ||
520 | |a CONCLUSIONS: Outcomes in the Veterans Affairs Health System were similar for African American and White men treated for low-intermediate-risk prostate cancer with AS | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a Research Support, U.S. Gov't, Non-P.H.S. | |
650 | 4 | |a African American | |
650 | 4 | |a Veterans Health Administration | |
650 | 4 | |a active surveillance | |
650 | 4 | |a clinical outcomes | |
650 | 4 | |a intermediate-risk prostate cancer | |
650 | 7 | |a Prostate-Specific Antigen |2 NLM | |
650 | 7 | |a EC 3.4.21.77 |2 NLM | |
700 | 1 | |a Deka, Rishi |e verfasserin |4 aut | |
700 | 1 | |a Kotha, Nikhil V |e verfasserin |4 aut | |
700 | 1 | |a Cherry, Daniel R |e verfasserin |4 aut | |
700 | 1 | |a Salans, Mia A |e verfasserin |4 aut | |
700 | 1 | |a Nelson, Tyler J |e verfasserin |4 aut | |
700 | 1 | |a Kumar, Abhishek |e verfasserin |4 aut | |
700 | 1 | |a Luterstein, Elaine |e verfasserin |4 aut | |
700 | 1 | |a Yip, Anthony T |e verfasserin |4 aut | |
700 | 1 | |a Nalawade, Vinit |e verfasserin |4 aut | |
700 | 1 | |a Parsons, J Kellogg |e verfasserin |4 aut | |
700 | 1 | |a Kader, A Karim |e verfasserin |4 aut | |
700 | 1 | |a Stewart, Tyler F |e verfasserin |4 aut | |
700 | 1 | |a Rose, Brent S |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Cancer |d 1948 |g 127(2021), 23 vom: 01. Dez., Seite 4403-4412 |w (DE-627)NLM000028649 |x 1097-0142 |7 nnns |
773 | 1 | 8 | |g volume:127 |g year:2021 |g number:23 |g day:01 |g month:12 |g pages:4403-4412 |
856 | 4 | 0 | |u http://dx.doi.org/10.1002/cncr.33824 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 127 |j 2021 |e 23 |b 01 |c 12 |h 4403-4412 |