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

被引:46
作者
Janssen, Boris V. [1 ,2 ]
Tutucu, Faik [1 ,3 ,4 ]
van Roessel, Stijn [2 ]
Adsay, Volkan [3 ,4 ]
Basturk, Olca [5 ]
Campbell, Fiona [6 ]
Doglioni, Claudio [7 ]
Esposito, Irene [8 ,9 ]
Feakins, Roger [10 ]
Fukushima, Noriyoshi [11 ]
Gill, Anthony J. [12 ,13 ]
Hruban, Ralph H. [14 ]
Kaplan, Jeffrey [15 ]
Koerkamp, Bas Groot [16 ]
Hong, Seung-Mo [17 ]
Krasinskas, Alyssa [18 ]
Luchini, Claudio [19 ]
Offerhaus, Johan [20 ]
Sarasqueta, Arantza Farina [1 ]
Shi, Chanjuan [21 ]
Singhi, Aatur [22 ]
Stoop, Thomas F. [2 ,23 ]
Soer, Eline C. [1 ]
Thompson, Elizabeth [14 ]
van Tienhoven, Geertjan [24 ]
Velthuysen, Marie-Louise F. [25 ]
Wilmink, Johanna W. [26 ]
Besselink, Marc G. [2 ]
Brosens, Lodewijk A. A. [20 ,27 ]
Wang, Huamin [28 ]
Verbeke, Caroline S. [29 ]
Verheij, Joanne [1 ]
机构
[1] Univ Amsterdam, Dept Pathol, Amsterdam UMC, Canc Ctr Amsterdam, Amsterdam, Netherlands
[2] Univ Amsterdam, Dept Surg, Amsterdam UMC, Canc Ctr Amsterdam, Amsterdam, Netherlands
[3] Koc Univ, Dept Pathol, Istanbul, Turkey
[4] KUTTAM Res Ctr, Istanbul, Turkey
[5] Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10021 USA
[6] Royal Liverpool Univ Hosp, Dept Pathol, Liverpool, Merseyside, England
[7] IRCCS San Raffaele Sci Inst, Dept Pathol, Milan, Italy
[8] Heinrich Heine Univ, Inst Pathol, Dusseldorf, Germany
[9] Univ Hosp Duesseldorf, Dusseldorf, Germany
[10] Royal Free London NHS Trust, Dept Pathol, London, England
[11] Jichi Med Univ Hosp, Dept Pathol, Shimotsuke, Tochigi, Japan
[12] Royal North Shore Hosp, Kolling Inst Med Res, Canc Diag & Pathol Grp, Sydney, NSW, Australia
[13] Univ Sydney, Sydney, NSW, Australia
[14] Johns Hopkins Univ, Sch Med, Dept Pathol, Sol Goldman Pancreat Canc Res Ctr, Baltimore, MD 21205 USA
[15] Univ Colorado Hosp, Dept Pathol, Denver, CO USA
[16] Erasmus MC, Dept Surg, Rotterdam, Netherlands
[17] Asan Med Ctr, Dept Pathol, Seoul, South Korea
[18] Emory Univ, Dept Pathol, Atlanta, GA 30322 USA
[19] Univ & Hosp Trust Verona, Dept Diagnost & Publ Hlth, Verona, Italy
[20] Univ Med Ctr Utrecht, Dept Pathol, Utrecht, Netherlands
[21] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[22] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA USA
[23] Univ Colorado, Dept Surg, Div Surg Oncol, Anschutz Med Campus, Aurora, CO USA
[24] Univ Amsterdam, Dept Radiat Oncol, Amsterdam UMC, Canc Ctr Amsterdam, Amsterdam, Netherlands
[25] Erasmus MC, Dept Pathol, Rotterdam, Netherlands
[26] Univ Amsterdam, Dept Med Oncol, Amsterdam UMC, Canc Ctr Amsterdam, Amsterdam, Netherlands
[27] Radboud UMC, Dept Pathol, Nijmegen, Netherlands
[28] Univ Texas MD Anderson Canc Ctr, Dept Anat Pathol, Houston, TX 77030 USA
[29] Univ Oslo, Inst Clin Med, Dept Pathol, Oslo, Norway
关键词
PREOPERATIVE CHEMORADIATION; DUCTAL ADENOCARCINOMA; RESIDUAL CARCINOMA; CHEMORADIOTHERAPY; SURVIVAL; CHALLENGES; ESOPHAGEAL; SURGERY; EXTENT;
D O I
10.1038/s41379-020-00683-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
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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页码:4 / 12
页数:9
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