Quantification of Gleason Pattern 4 Metrics Identifies Pathologic Progression in Patients With Grade Group 2 Prostate Cancer on Active Surveillance

IF 2.3 3区 医学 Q3 ONCOLOGY
Marlon Perera , Melissa Assel , Sunny Nalavenkata , Sari Khaleel , Nicole Benfante , Sigrid V. Carlsson , Victor E. Reuter , Vincent P. Laudone , Peter T. Scardino , Karim A. Touijer , James A. Eastham , Andrew J. Vickers , Samson W. Fine , Behfar Ehdaie
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引用次数: 0

Abstract

Background

During active surveillance (AS) for Grade Group (GG) 2 prostate cancer, pathologic progression to GG3 on surveillance biopsy is a trigger for intervention. However, this ratio of GP3:GP4, may be obscured by increases of relatively indolent disease. We aimed to explore changes in GP4 quantity during AS and propose alternative definitions for progression based on GP4 changes.

Design, Setting, and Participants

We assessed patients enrolled on AS between November 2014 and March 2020 with GG2 disease on diagnostic biopsy and subsequent surveillance biopsy approximately 1 year later. Outcome measures included change in overall %GP4 and total length GP4 (mm).

Results and Limitations

61 patients met the inclusion criteria, the median change in total length of GP4 and %GP4 was -0.12 mm (IQR −0.31, 0.09) and −2.5% (IQR −8.6, 0.0), respectively. Excluding the 35 patients with no evidence of GP4 on surveillance biopsy, median change in total GP4 length and %GP4 was 0.19 mm (IQR −0.04, 0.67) and 1.2% (IQR −1.6, 6.6), respectively. Three patients progressed to GG3 disease on surveillance biopsy, one of whom had only a small increase in %GP4. Conversely, an additional 2 patients who did not meet the criterion for GG3 had a large increase (> 1 mm) in total GP4 length.

Conclusions

Presence of GG3 disease on surveillance biopsy as a trigger for treatment in men on AS is of questionable use alone; we suggest including other measures that do not depend on a ratio, such as an increase in total GP4 length.

对格里森模式 4 指标的量化可识别接受主动监测的 2 级前列腺癌患者的病理进展情况
背景在对2级前列腺癌(GG)进行主动监测(AS)期间,监测活检的病理进展为GG3时,就需要进行干预。然而,GP3:GP4的这一比例可能会被相对缓和疾病的增加所掩盖。我们旨在探索AS期间GP4数量的变化,并根据GP4的变化提出进展的替代定义。设计、设置和参与者我们评估了2014年11月至2020年3月期间入组AS的患者,这些患者在诊断性活检中患有GG2疾病,并在大约1年后进行了后续的监测性活检。结果测量指标包括总体GP4%和GP4总长度(毫米)的变化。结果和局限性61例患者符合纳入标准,GP4总长度和GP4%的中位变化分别为-0.12毫米(IQR -0.31,0.09)和-2.5%(IQR -8.6,0.0)。剔除监测活检未发现 GP4 的 35 例患者,GP4 总长度和 GP4 百分比的中位变化分别为 0.19 毫米(IQR -0.04,0.67)和 1.2%(IQR -1.6,6.6)。三名患者在监测活检时发展为 GG3 病变,其中一人的 GP4 百分比仅略有增加。结论在监测活检中出现 GG3 病变作为男性 AS 患者治疗的触发因素,仅此一项的作用值得怀疑;我们建议纳入其他不依赖于比值的指标,如 GP4 总长度的增加。
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来源期刊
Clinical genitourinary cancer
Clinical genitourinary cancer 医学-泌尿学与肾脏学
CiteScore
5.20
自引率
6.20%
发文量
201
审稿时长
54 days
期刊介绍: Clinical Genitourinary Cancer is a peer-reviewed journal that publishes original articles describing various aspects of clinical and translational research in genitourinary cancers. Clinical Genitourinary Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of genitourinary cancers. The main emphasis is on recent scientific developments in all areas related to genitourinary malignancies. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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