ArticleEuropean journal of nuclear medicine and molecular imaging2026
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Article 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. Cited by 1 paper, 1 of them a synthesis that pooled it.
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
1 citing paper in PubMed, 1 synthesis or guideline pooled it.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeThis study evaluates the prognostic value of early response assessment using the Response Evaluation Criteria in PSMA imaging (RECIP 1.0) applied to 24-hour post-therapy SPECT/CT at the second cycle of lutetium-177 (
methodsThis analysis included 136 metastatic castration-resistant prostate cancer (mCRPC) patients treated with ≥ 2 cycles of [
resultsAfter a median follow-up of 23 months, median PSA-PFS was 6.4 months and median OS was 16.6 months. Regarding imaging parameters, increase in SUVmean (HR = 1.02, p < 0.001), TTV increase ≥ 20% (HR = 3.5, p < 0.001) and appearance of new lesions (NL) (HR = 2.6, p < 0.001) were significantly associated with shorter PSA-PFS, while only TTV increase ≥ 20% (HR = 1.8, p = 0.023) and NLs (HR = 2.3, p = 0.0016) were associated with OS. The combination of both categories using RECIP 1.0 demonstrated that RECIP-PD patients (n = 16/136) had significantly reduced median PSA-PFS (HR = 3.6, p < 0.001) and OS (HR = 3.1, p < 0.001) compared to RECIP-non-PD. The most consistent prognostic accuracy was achieved using RECIP 1.0 (Harrell's C-index: PSA-PFS = 0.80, OS = 0.78).
conclusionOur study demonstrates that quantitative RECIP 1.0 applied on C2 [
Indexed as
Identifiers
41207904What OpenQuestion 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 OpenQuestion graph.