TY - JOUR
T1 - First postoperative PSA is associated with outcomes in patients with node positive prostate cancer
T2 - Results from the SEARCH database
AU - McDonald, Michelle L.
AU - Howard, Lauren E.
AU - Aronson, William J.
AU - Terris, Martha K.
AU - Cooperberg, Matthew R.
AU - Amling, Christopher L.
AU - Freedland, Stephen J.
AU - Kane, Christopher J.
N1 - Funding Information:
Dr. William Aronson is partially supported by the NIH/NCI Grant P50CA09231 and Dr. Freedland is supported by NIH K24 CA160653
PY - 2018/5
Y1 - 2018/5
N2 - Objective: To analyze factors associated with metastases, prostate cancer-specific mortality, and all-cause mortality in pN1 patients. Materials and methods: We analyzed 3,642 radical prostatectomy patients within the Shared Equal Access Regional Cancer Hospital (SEARCH) database. Pathologic Gleason grade, number of lymph nodes (LN) removed, and first postoperative prostate-specific antigen (PSA) (<0.2 ng/ml or ≥0.2 ng/ml) were among covariates assessed. Cox regression was used to analyze the association between characteristics and survival outcomes. Kaplan-Meier was used to estimate survival in pN1 patients stratified by first postoperative PSA. Results: Of 3,642 patients, 124 (3.4%) had pN1. There were 71 (60%) patients with 1 positive LN, 32 (27%) with 2 positive LNs, and 15 (13%) with ≥3. Among men with pN1, first postoperative PSA was<0.2 ng/ml in 46 patients (51%) and ≥0.2 ng/ml in 44 patients (49%). Univariable Cox regression determined pathological Gleason grade (P = 0.021), seminal vesicle invasion (P = 0.010), and first postoperative PSA ≥0.2 ng/ml (P = 0.005) were associated with metastases. First postoperative PSA ≥0.2 ng/ml was associated with metastasis on multivariable analysis (P = 0.046). Log-rank analysis revealed a more favorable metastases-free survival in patients with a first postoperative PSA<0.2 ng/ml (P = 0.001). Estimated 5-year metastases-free survival rate was 99% for patients with a first postoperative PSA<0.2 ng/ml and 87% for ≥0.2 ng/ml. Conclusions: pN1 patients with a first postoperative PSA ≥0.2 ng/ml were more likely to develop metastases. First postoperative PSA may be useful in identifying pN1 patients who harbor distant disease and aid in secondary treatment decisions.
AB - Objective: To analyze factors associated with metastases, prostate cancer-specific mortality, and all-cause mortality in pN1 patients. Materials and methods: We analyzed 3,642 radical prostatectomy patients within the Shared Equal Access Regional Cancer Hospital (SEARCH) database. Pathologic Gleason grade, number of lymph nodes (LN) removed, and first postoperative prostate-specific antigen (PSA) (<0.2 ng/ml or ≥0.2 ng/ml) were among covariates assessed. Cox regression was used to analyze the association between characteristics and survival outcomes. Kaplan-Meier was used to estimate survival in pN1 patients stratified by first postoperative PSA. Results: Of 3,642 patients, 124 (3.4%) had pN1. There were 71 (60%) patients with 1 positive LN, 32 (27%) with 2 positive LNs, and 15 (13%) with ≥3. Among men with pN1, first postoperative PSA was<0.2 ng/ml in 46 patients (51%) and ≥0.2 ng/ml in 44 patients (49%). Univariable Cox regression determined pathological Gleason grade (P = 0.021), seminal vesicle invasion (P = 0.010), and first postoperative PSA ≥0.2 ng/ml (P = 0.005) were associated with metastases. First postoperative PSA ≥0.2 ng/ml was associated with metastasis on multivariable analysis (P = 0.046). Log-rank analysis revealed a more favorable metastases-free survival in patients with a first postoperative PSA<0.2 ng/ml (P = 0.001). Estimated 5-year metastases-free survival rate was 99% for patients with a first postoperative PSA<0.2 ng/ml and 87% for ≥0.2 ng/ml. Conclusions: pN1 patients with a first postoperative PSA ≥0.2 ng/ml were more likely to develop metastases. First postoperative PSA may be useful in identifying pN1 patients who harbor distant disease and aid in secondary treatment decisions.
KW - Lymph node
KW - Metastases
KW - PSA
KW - Prostate neoplasms
KW - Prostatectomy
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U2 - 10.1016/j.urolonc.2018.01.005
DO - 10.1016/j.urolonc.2018.01.005
M3 - Article
C2 - 29429895
AN - SCOPUS:85041647250
SN - 1078-1439
VL - 36
SP - 239.e17-239.e25
JO - Urologic Oncology: Seminars and Original Investigations
JF - Urologic Oncology: Seminars and Original Investigations
IS - 5
ER -