Observational studyEuropean journal of nuclear medicine and molecular imaging2026
Impact of radium-223 on bone imaging and biochemical markers with and without bone-modifying agents in bone-metastatic castration-resistant prostate cancer: results from the kyucog-1901 study.
Observational study in European journal of nuclear medicine and molecular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
15 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundRadium-223 dichloride (Ra-223) improves survival in men with metastatic castration-resistant prostate cancer (mCRPC) and bone metastases, but its interaction with bone-modifying agents remains unclear.
methodsThe KYUCOG-1901 prospective multicenter study enrolled Japanese men with mCRPC and bone metastases treated with up to six cycles of Ra-223. Serial assessments included bone scan index (BSI), serum bone metabolic markers (BMMs; BAP, P1NP, and TRACP-5b), and bone mineral density (BMD) from baseline (BL) through one year. Clinical outcomes including radiographic progression-free survival (rPFS), time to symptomatic skeletal event and overall survival were assessed by BSI and serum BMMs.
resultsBSI remained stable throughout treatment and follow-up. High BL BSI predicted early discontinuation and shorter rPFS, and increases in BSI correlated with worse rPFS. BAP exhibited a transient decline in patients treated with and without bone-modifying agents (BMAs), while TRACP-5b declined in those receiving BMAs. Elevated BAP at BL and BMMs at end of treatment, and increases in P1NP during therapy, were associated with rPFS. Lumbar spine BMD increased modestly over 1 year in both patients treated with and without BMAs, while femoral BMD remained unchanged.
conclusionRa-223 stabilized skeletal tumor burden, transiently suppressed serum BMMs, and improved lumbar BMD in men with mCRPC. BSI and serum BMMs provided prognostic information, supporting their integration into longitudinal monitoring. These findings highlight the potential of combining Ra-223 with bone-modifying agents to optimize outcomes.
Indexed as
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.