从病理学角度重新命名1级组前列腺“癌”:呼吁多学科讨论。

IF 5.1 2区 医学 Q1 PATHOLOGY
Gladell P Paner, Ming Zhou, Jeffry P Simko, Scott E Eggener, Theodorus van der Kwast
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引用次数: 1

摘要

尽管在提高低级别前列腺癌的智能筛查和保守管理方面取得了创新,但过度诊断和过度治疗仍然是一个主要的卫生保健问题。在减少对患者伤害的主要目标的驱动下,对非致死性1级(GG 1)前列腺癌进行重新标记的建议已经提出,但面临着临床医生和病理学家不同程度的支持和反对。GG - 1肿瘤表现出癌症的组织学(侵袭性)和分子特征,但矛盾的是,如果是纯粹的,就不能转移,很少延伸出前列腺,如果切除,癌症特异性生存率接近100%。大多数反对重新标记GG - 1的论点都与活检中未采样区域丢失更高级别成分的担忧有关。然而,肿瘤的良性或恶性的指定不应该基于诊断程序的缺点和抽样错误。本综述探讨了可能的解决方案,主要是在根治性前列腺切除术(RP)中重新命名GG 1的可行性,以及活检诊断的影响,病理学家和临床医生都可以接受。一种可行的方法是使用“明确的标准”将RP中的GG 1重新命名为谨慎的中性或非良性非癌症术语(例如,腺泡性肿瘤),这将阻止活检中每一个GG 1不加区分地报告为癌症,包括RP中最终不明显的微肿瘤。在活检中使用相应的不确定术语,同时评论样本不足的非无痛性癌症的可能性,可能会减少病理学家对升级的担忧。在活组织检查中去掉“癌”这个词,可以避免给病人贴上癌症标签的负面后果,包括不必要的明确治疗(过度治疗的根本原因)。重命名应保持当前分级和风险分层管理算法的现状,同时尽量减少过度治疗。然而,找到这个问题答案的最佳方法是通过关键利益相关者的多学科讨论,特别关注以患者为中心的问题及其在我们实践中的影响。GG 1重命名在过去已经被提出,尽管有持续的反对意见,如果不更全面地解决,可能会继续出现过度诊断,过度治疗和患者的痛苦持续。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Renaming Grade Group 1 Prostate "Cancer" From a Pathology Perspective: A Call for Multidisciplinary Discussion.

Despite the innovations made to enhance smarter screening and conservative management for low-grade prostate cancer, overdiagnosis, and overtreatment remains a major health care problem. Driven by the primary goal of reducing harm to the patients, relabeling of nonlethal grade group 1 (GG 1) prostate cancer has been proposed but faced varying degrees of support and objection from clinicians and pathologists. GG 1 tumor exhibits histologic (invasive) and molecular features of cancer but paradoxically, if pure, is unable to metastasize, rarely extends out of the prostate, and if resected, has a cancer-specific survival approaching 100%. Most of the arguments against relabeling GG 1 relate to concerns of missing a higher-grade component through the unsampled area at biopsy. However, the designation of tumor benignity or malignancy should not be based on the shortcomings of a diagnostic procedure and sampling errors. This review explores possible solutions, mainly the feasibility of renaming GG 1 in radical prostatectomy (RP) with ramifications in biopsy diagnosis, acceptable for both pathologists and clinicians. One workable approach is to rename GG 1 in RP with a cautious neutral or nonbenign non-cancer term (eg, acinar neoplasm) using "defined criteria" that will stop the indiscriminate reporting of every GG 1 in biopsy as carcinoma including eventual insignificant microtumors in RPs. Use of a corresponding noncommittal term at biopsy while commenting on the possibility of an undersampled nonindolent cancer, might reduce the pathologist's concerns about upgrading. Dropping the word "carcinoma" in biopsy preempts the negative consequences of labeling the patient with cancer, including unnecessary definitive therapy (the root cause of overtreatment). Renaming should retain the status quo of contemporary grading and risk stratifications for management algorithms while trying to minimize overtreatment. However, the optimal approach to find answers to this issue is through multidisciplinary discussions of key stakeholders with a specific focus on patient-centered concerns and their ramifications in our practices. GG 1 renaming has been brought up in the past and came up again despite the continued counterarguments, and if not addressed more comprehensively will likely continue to reemerge as overdiagnosis, overtreatment, and patient's sufferings persist.

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来源期刊
CiteScore
10.30
自引率
3.00%
发文量
88
审稿时长
>12 weeks
期刊介绍: Advances in Anatomic Pathology provides targeted coverage of the key developments in anatomic and surgical pathology. It covers subjects ranging from basic morphology to the most advanced molecular biology techniques. The journal selects and efficiently communicates the most important information from recent world literature and offers invaluable assistance in managing the increasing flow of information in pathology.
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