Follicular lymphoma research: an open dialogue for a collaborative roadmap.

IF 3.9 2区 医学 Q2 CELL BIOLOGY Histopathology Pub Date : 2024-10-29 DOI:10.1111/his.15344
Mélanie Collin, Guillemette Gagey, Vignesh Shanmugam, Abner Louissaint, Jessica Okosun, Clementine Sarkozy, Bertrand Nadel
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Abstract

Follicular lymphoma (FL) is the second most common type of lymphoma (20% of all non-Hodgkin lymphomas), derived from germinal centre (GC) B cells, and is characterised by its significant clinical, prognostic and biological heterogeneity, leading to complexity in management. Despite significant biological investigation and indisputable clinical progress since the advent of the immunotherapy era more than 20 years ago, much remains to be done to understand and cure this lymphoma. Today, FL is metaphorically a giant puzzle on the table with patches of sky, landscape and foliage clearly appearing. However, many of the remaining pieces are held by various stakeholders (e.g. clinicians, pathologists, researchers, drug developers) without global agreement on what the gaps are, or any clear blueprint on how to solve the puzzle of understanding the heterogeneity of this disease and create curative and tailored therapies. With the advent of new investigation and drug technologies, together with recent advances in our capacity to manage big data, the time seems ripe for a change of scale. More than ever, this will require collaboration between and within all stakeholders to overcome the current bottlenecks in the field. As for every investigator, we acknowledge that this first draft is necessarily biased, incomplete and some FL expert readers might recognise some remaining gaps not addressed. We hope they will reply to make this effort a collaborative one to assemble all the pieces in the most ideal fashion. As such, this review intends to be a first step and an interactive platform to a collaborative roadmap towards better understanding and care of FL.

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滤泡性淋巴瘤研究:为制定合作路线图而开展的公开对话。
滤泡性淋巴瘤(FL)是第二大常见类型的淋巴瘤(占所有非霍奇金淋巴瘤的20%),来源于生殖中心(GC)B细胞,其特点是临床、预后和生物学异质性显著,导致治疗的复杂性。自 20 多年前免疫疗法时代到来以来,尽管进行了大量生物学研究并取得了无可争议的临床进展,但要了解和治愈这种淋巴瘤仍有许多工作要做。如今,FL 就像摆在桌面上的一幅巨大拼图,天空、风景和树叶都清晰可见。然而,剩下的许多碎片被不同的利益相关者(如临床医生、病理学家、研究人员、药物开发人员等)所掌握,全球对其中的差距尚未达成一致意见,也没有明确的蓝图来说明如何解决这一难题,了解这种疾病的异质性,并创造出治疗性和量身定制的疗法。随着新的调查和药物技术的出现,以及我们管理大数据能力的最新进展,改变规模的时机似乎已经成熟。这将比以往任何时候都更需要所有利益相关者之间和内部的合作,以克服该领域目前存在的瓶颈。对于每一位研究人员,我们承认这篇初稿必然有失偏颇、不完整,一些 FL 专家读者可能会认识到一些尚未解决的差距。我们希望他们能给予回复,使这项工作成为一项合作,以最理想的方式汇集所有碎片。因此,这篇综述旨在成为迈向更好地理解和护理 FL 的第一步和互动平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Histopathology
Histopathology 医学-病理学
CiteScore
10.20
自引率
4.70%
发文量
239
审稿时长
1 months
期刊介绍: Histopathology is an international journal intended to be of practical value to surgical and diagnostic histopathologists, and to investigators of human disease who employ histopathological methods. Our primary purpose is to publish advances in pathology, in particular those applicable to clinical practice and contributing to the better understanding of human disease.
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