Evaluating the association between bone pain and radiologic progression-free survival (rPFS) in patients with metastatic castration-sensitive prostate cancer (mCSPC).

94 Background: Previous studies have shown bone pain to be associated with worse survival in patients with metastatic castration-resistant prostate cancer (mCRPC). However, there are few data regarding bone pain and survival outcomes in patients with (mCSPC). In the current study, we evaluated the association between bone pain and rPFS in patients treated with mCSPC. Methods: rPFS were estimated by using the Kaplan-Meier method and the log-rank test was used for the comparison between different subgroups. Differences in baseline characteristics by bone pain status at mHSPC were evaluated with χ2 test for categorical variables. Results: Data from 205 patients were analyzed. A detail of the patient’s characteristics is shown (Table).The median rPFS for all populations was calculated as 24 mo. In univariate analysis, the median rPFS were 17 vs 29.5 mo in patients with bone pain presentations vs none-pain (p=0.001), 29 vs 20 mo in patients with ECOG PS 0 or 1≥ (p=0.09), 22 vs 14 mo in patients with DNA repair mutations absent and present(p=0.06), 27 mo vs 19 mo in patients with low volume presentation vs high volume (p=0.05), 15 vs 25 months in patients with or without liver metastases (p=0.003), 17 mo vs 27 mo in patients with hemoglobin levels <12 gr/dL or higher (p=0.002), respectively. In multivariate analysis, bone pain (HR 1.9; 95% CI 1.2-3.1; p:0.001), hemoglobin<12 gr/dL (HR 2; 95% CI 1.9 -3.1; p:0.005) were found to be an independent determinant of short rPFS. Conclusions: Bone pain is associated with short rPFS in mCSPC. The current study showed bone pain needs to be selected in the treatment choice or prognostic model in mCSPC. Baseline characteristics of patients. Variable Patients Presence of bone pain Absence of bone pain (n=104) (n=101) p value ECOG performance status, n(%), p 0 ≥1 34 (%32.7)70 (%67.3) 67 (%66.3)34 (%33.7) <0,001 Gleason score at diagnosis, n(%), p <8 ≥8 Unknown 31 (%29.8)66 (%63.5)7 (%6.7) 34 (%33.7)65 (%64.4)2 (%1.9) 0,723 Under/over 70 years old, n(%), p <70 years ≥70 years 40 (%38.5)64 (%61.5) 47 (%46.5)54 (%53.5) 0,242 High/low volume disease, n(%), p High volume Low volume 76 (%73.1)28 (%26.9) 29 (%28.7)72 (%71.3) <0,001 Metastasis at diagnosis, n(%), p Yes No 79 (%76)25 (%24) 64 (%63.4)37 (%36.6) 0,050 Metachronous metastasis, n(%), p Yes No 25 (%24)79 (%76) 36 (%35.6)65 (%64.4) 0,069 Liver metastasis at diagnosis, n(%), p Yes No 9 (%8.7)95 (%91.3) 0 (%0)101 (%100) 0,002 DNA repair mutation, n(%), p Positive Negative Unknown 10 (%9.6)38 (%36.5)56 (%53.9) 5 (%5)38 (%37.6)58 (%57.4) 0,436 Hemoglobin levels, n(%), p <12 gr/dL ≥12 gr/dL Unknown 30 (%28.8)61 (%58.7)13 (%12.5) 20 (%19.8)74 (%73.3)7 (%6.9) 0,073 PSA levels, n(%), p <17 ng/ml ≥17 ng/ml 46 (%44.2)58 (%55.8) 56 (%55.4)45 (%44.6) 0,094 First line treatment 0.08 Androgen receptor pathway inhibitor 43 (%41.3) 45 (%44.6) Only ADT 34 (%32.7) 42 (%41.6) Docetaxel

Authors

Institutions

Publication Details

Journal
Journal of Clinical Oncology
Published
2025-02-10
DOI
https://doi.org/10.1200/jco.2025.43.5_suppl.94
Primary Topic
Prostate Cancer Treatment and Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Evaluating the association between bone pain and radiologic progression-free survival (rPFS) in patients with metastatic castration-sensitive prostate cancer (mCSPC).

Volkan Tuğcu, Kamil Gökhan Şeker, Caner Kapar, Selçuk Şahin et al.
1 links
Journal of Clinical Oncology
Prostate Cancer Treatment and Research
article

Evaluating the association between bone pain and radiologic progression-free survival (rPFS) in patients with metastatic castration-sensitive prostate cancer (mCSPC).

Volkan Tuğcu, Kamil Gökhan Şeker, Caner Kapar, Selçuk Şahin, Deniz Tural
article en

Abstract

94 Background: Previous studies have shown bone pain to be associated with worse survival in patients with metastatic castration-resistant prostate cancer (mCRPC). However, there are few data regarding bone pain and survival outcomes in patients with (mCSPC). In the current study, we evaluated the association between bone pain and rPFS in patients treated with mCSPC. Methods: rPFS were estimated by using the Kaplan-Meier method and the log-rank test was used for the comparison between different subgroups. Differences in baseline characteristics by bone pain status at mHSPC were evaluated with χ2 test for categorical variables. Results: Data from 205 patients were analyzed. A detail of the patient’s characteristics is shown (Table).The median rPFS for all populations was calculated as 24 mo. In univariate analysis, the median rPFS were 17 vs 29.5 mo in patients with bone pain presentations vs none-pain (p=0.001), 29 vs 20 mo in patients with ECOG PS 0 or 1≥ (p=0.09), 22 vs 14 mo in patients with DNA repair mutations absent and present(p=0.06), 27 mo vs 19 mo in patients with low volume presentation vs high volume (p=0.05), 15 vs 25 months in patients with or without liver metastases (p=0.003), 17 mo vs 27 mo in patients with hemoglobin levels <12 gr/dL or higher (p=0.002), respectively. In multivariate analysis, bone pain (HR 1.9; 95% CI 1.2-3.1; p:0.001), hemoglobin<12 gr/dL (HR 2; 95% CI 1.9 -3.1; p:0.005) were found to be an independent determinant of short rPFS. Conclusions: Bone pain is associated with short rPFS in mCSPC. The current study showed bone pain needs to be selected in the treatment choice or prognostic model in mCSPC. Baseline characteristics of patients. Variable Patients Presence of bone pain Absence of bone pain (n=104) (n=101) p value ECOG performance status, n(%), p 0 ≥1 34 (%32.7)70 (%67.3) 67 (%66.3)34 (%33.7) <0,001 Gleason score at diagnosis, n(%), p <8 ≥8 Unknown 31 (%29.8)66 (%63.5)7 (%6.7) 34 (%33.7)65 (%64.4)2 (%1.9) 0,723 Under/over 70 years old, n(%), p <70 years ≥70 years 40 (%38.5)64 (%61.5) 47 (%46.5)54 (%53.5) 0,242 High/low volume disease, n(%), p High volume Low volume 76 (%73.1)28 (%26.9) 29 (%28.7)72 (%71.3) <0,001 Metastasis at diagnosis, n(%), p Yes No 79 (%76)25 (%24) 64 (%63.4)37 (%36.6) 0,050 Metachronous metastasis, n(%), p Yes No 25 (%24)79 (%76) 36 (%35.6)65 (%64.4) 0,069 Liver metastasis at diagnosis, n(%), p Yes No 9 (%8.7)95 (%91.3) 0 (%0)101 (%100) 0,002 DNA repair mutation, n(%), p Positive Negative Unknown 10 (%9.6)38 (%36.5)56 (%53.9) 5 (%5)38 (%37.6)58 (%57.4) 0,436 Hemoglobin levels, n(%), p <12 gr/dL ≥12 gr/dL Unknown 30 (%28.8)61 (%58.7)13 (%12.5) 20 (%19.8)74 (%73.3)7 (%6.9) 0,073 PSA levels, n(%), p <17 ng/ml ≥17 ng/ml 46 (%44.2)58 (%55.8) 56 (%55.4)45 (%44.6) 0,094 First line treatment 0.08 Androgen receptor pathway inhibitor 43 (%41.3) 45 (%44.6) Only ADT 34 (%32.7) 42 (%41.6) Docetaxel

Journal of Clinical OncologyVol. 43(5_suppl)
Koç University (TR), Bakırköy Psychiatric Hospital (TR), Istinye University (TR), Liv Hospital (TR)
Openalex Percentile: Top 95%
Prostate Cancer Treatment and Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.