Amsterdam International Consensus Meeting: tumor response scoring in the pathology assessment of resected pancreatic cancer after neoadjuvant therapy

医学 新辅助治疗 胰腺癌 辅助治疗 癌症 采样(信号处理) 组织病理学 肿瘤科 病理 医学物理学 内科学 乳腺癌 计算机科学 计算机视觉 滤波器(信号处理)
作者
Boris V. Janssen,Faik Tutucu,Stijn van Roessel,Volkan Adsay,Olca Baştürk,Fiona Campbell,Claudio Doglioni,Iréne Esposito,Roger Feakins,Noriyoshi Fukushima,Anthony J. Gill,Ralph H. Hruban,Jeffrey Kaplan,Bas Groot Koerkamp,Seung‐Mo Hong,Alyssa M. Krasinskas,Claudio Luchini,Johan Offerhaus,Arantza Fariña Sarasqueta,Chanjuan Shi
出处
期刊:Modern Pathology [Elsevier BV]
卷期号:34 (1): 4-12 被引量:50
标识
DOI:10.1038/s41379-020-00683-9
摘要

Histopathologically scoring the response of pancreatic ductal adenocarcinoma (PDAC) to neoadjuvant treatment can guide the selection of adjuvant therapy and improve prognostic stratification. However, several tumor response scoring (TRS) systems exist, and consensus is lacking as to which system represents best practice. An international consensus meeting on TRS took place in November 2019 in Amsterdam, The Netherlands. Here, we provide an overview of the outcomes and consensus statements that originated from this meeting. Consensus (≥80% agreement) was reached on a total of seven statements: (1) TRS is important because it provides information about the effect of neoadjuvant treatment that is not provided by other histopathology-based descriptors. (2) TRS for resected PDAC following neoadjuvant therapy should assess residual (viable) tumor burden instead of tumor regression. (3) The CAP scoring system is considered the most adequate scoring system to date because it is based on the presence and amount of residual cancer cells instead of tumor regression. (4) The defining criteria of the categories in the CAP scoring system should be improved by replacing subjective terms including "minimal" or "extensive" with objective criteria to evaluate the extent of viable tumor. (5) The improved, consensus-based system should be validated retrospectively and prospectively. (6) Prospective studies should determine the extent of tissue sampling that is required to ensure adequate assessment of the residual cancer burden, taking into account the heterogeneity of tumor response. (7) In future scientific publications, the extent of tissue sampling should be described in detail in the "Materials and methods" section.
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