Alfred Honoré, Karsten Gravdal, Patrick Juliebø-Jones, Lars Anders Rokne Reisæter, Christian Beisland, Christian Arvei Moen
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引用次数: 0
Abstract
Objective
Transrectal (TR) prostate biopsy is being increasingly abandoned in favour of a transperineal (TP) approach as well as a targeted biopsy only of the index lesion(s). It remains underreported how these changes could impact concordance at final pathology. We aimed to evaluate the impact of transitioning from standard transrectal (sTR) to cognitive targeted transperineal (cog-tTP) biopsy on final pathology including concordance and upgrading.
Material and methods
Analysis of consecutive patients undergoing prostate biopsy and prostatectomy (RP) between January 2018 and May 2022 at a tertiary centre in Western Norway.
Results
There were 210 and 239 patients in the sTR and cog-tTP groups, respectively. The mean [IQR] number of biopsies decreased from 12 [4–12] to 3 [3–4] (p < 0.001). The overall rate of concordance between biopsy and final pathology was 64% in both groups (Table 3, Figure 1). 24% Twenty-four per cent (cog-tTP) versus 19% (sTR) had grade group (GG) upgrading, while 12% versus 17% were downgraded (p = 0.2). Regarding positive surgical margins (PSMs) that were >3 mm in extension, there were only 3.3% and 2.1% in the sTR and cog-tTP groups, respectively (p = 0.4). For surgical outcomes associated with RP, no differences in terms of postoperative complications between the groups were found (cog-tTP:10% vs. sTR:6%, p = 0.10).
Conclusion
Transitioning from sTR biopsy to targeted cog-tTP biopsy does not compromise concordance at final pathology nor does it increase the risk of tumour upgrading.
目的:经直肠(TR)前列腺活检越来越多地被放弃,转而采用经会阴(TP)方法以及仅针对指数病变的靶向活检。这些改变如何影响最终病理的一致性仍未被充分报道。我们旨在评估从标准经直肠活检(sTR)过渡到认知靶向经会阴活检(cog-tTP)对最终病理的影响,包括一致性和升级。材料和方法:分析2018年1月至2022年5月在挪威西部三级中心连续接受前列腺活检和前列腺切除术(RP)的患者。结果:sTR组210例,cog-tTP组239例。平均[IQR]活检次数由12例[4-12]降至3例[3-4](p p = 0.2)。阳性手术切缘(psm)扩展为bbb30 mm, sTR组和cog-tTP组分别只有3.3%和2.1% (p = 0.4)。对于RP相关的手术结果,两组之间的术后并发症没有差异(cog-tTP:10% vs. sTR:6%, p = 0.10)。结论:从sTR活检过渡到靶向cog-tTP活检不会损害最终病理的一致性,也不会增加肿瘤升级的风险。