TY - JOUR
T1 - Results of a worldwide survey on the currently used histopathological diagnostic criteria for invasive lobular breast cancer
AU - De Schepper, Maxim
AU - Vincent-Salomon, Anne
AU - Christgen, Matthias
AU - Van Baelen, Karen
AU - Richard, François
AU - Tsuda, Hitoshi
AU - Kurozumi, Sasagu
AU - Brito, Maria Jose
AU - Cserni, Gabor
AU - Schnitt, Stuart
AU - Larsimont, Denis
AU - Kulka, Janina
AU - Fernandez, Pedro Luis
AU - Rodríguez-Martínez, Paula
AU - Olivar, Ana Aula
AU - Melendez, Cristina
AU - Van Bockstal, Mieke
AU - Kovacs, Aniko
AU - Varga, Zsuzsanna
AU - Wesseling, Jelle
AU - Bhargava, Rohit
AU - Boström, Pia
AU - Franchet, Camille
AU - Zambuko, Blessing
AU - Matute, Gustavo
AU - Mueller, Sophie
AU - Berghian, Anca
AU - Rakha, Emad
AU - van Diest, Paul J.
AU - Oesterreich, Steffi
AU - Derksen, Patrick W.B.
AU - Floris, Giuseppe
AU - Desmedt, Christine
N1 - Funding Information:
The authors wish to thank all the pathologists who consented of being acknowledged: Gabriela Acosta Haab, Georges Aftimos, Wiebke Antonopoulos, Laurent Arnould, Leart Berdica, Laia Bernet Vegué, Rohit Bhargava, Peter Bult, Benjamin Calhoun, Marie-Pierre Chenard, Cecile Colpaert, Alicia Cordoba, Franceska Dedeurwaerdere, James Degaetano, Raphaëlle Duprez, Gelareh Farshid, Pedro L. Fernandez, Bolorerdene Gantumur, Nina Helidon, Akira I. Hida, Naoko Honma, Rie Horii, Endre Kalman, Naoki Kanomata, Ayaka Katayama, Yuka Katsurada, Tomonori Kawasaki, Anikó Kovács, Glen Kristiansen, Hajime Kuroda, Masafumi Kurosumi, Konrad Kurowski, Inta Liepniece-Karele, Patricia Lopez Correa, Robert Lukande, Gaetan Macgrogan, Aurélie Maran-Gonzalez, Takuya Moriya, Anupma Nayak, Yasuyo Ohi, Tomo Osako, Tetsunari Oyama, Alberto Ravarino, Peter Regitnig, Elisabeth Russ, Takashi Sakatani, Sandra Sarancone, Anne-Marie Schelfhout, Marcia Silveira- Graudenz, Luz F. Sua Villegas, Miklos Torok, Joost Van Gorp, Zsuzsanna Varga, Andras Vörös, Willem Vreuks, Clive Wells, Pieter Westenend, Suzanne Wilhelmus, Rin Yamaguchi.
Funding Information:
H.T.: recipient of scholarship donation from Chugai, Takeda, and Eli Lily and of research grant from Roche Diagnostics. S.K.: has received honoraria from Daiichi Sankyo co. ltd, Taiho Pharmaceutical co. ltd, Eli Lilly and Company, MSD K.K., AstraZeneca K.K., Chugai Pharmaceutical, Ltd., Dinow Inc., and Novartis Japan.A. Kovacs: received honoraria from Pfizer and R.J.W.: receives funding from KWF Dutch Cancer Society, Cancer Research UK, Antoni van Leeuwenhoek Investment Fund, ZonMw Health Care Innovation funding from the Dutch government. G.F.: recipient of a post-doctoral fellowship sponsored by the KOOR from University Hospitals Leuven. P.D.: received funding from Pfizer, ZonMw Health Care Innovation from the Dutch government, University Utrecht.
Funding Information:
This publication is partly based upon work from COST action LOBSTERPOT (CA19138), supported by COST (European Cooperation in Science and Technology). KVB and MDS are funded by the KU Leuven Fund Nadine de Beauffort.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Invasive lobular carcinoma (ILC) represents the second most common subtype of breast cancer (BC), accounting for up to 15% of all invasive BC. Loss of cell adhesion due to functional inactivation of E-cadherin is the hallmark of ILC. Although the current world health organization (WHO) classification for diagnosing ILC requires the recognition of the dispersed or linear non-cohesive growth pattern, it is not mandatory to demonstrate E-cadherin loss by immunohistochemistry (IHC). Recent results of central pathology review of two large randomized clinical trials have demonstrated relative overdiagnosis of ILC, as only ~60% of the locally diagnosed ILCs were confirmed by central pathology. To understand the possible underlying reasons of this discrepancy, we undertook a worldwide survey on the current practice of diagnosing BC as ILC. A survey was drafted by a panel of pathologists and researchers from the European lobular breast cancer consortium (ELBCC) using the online tool SurveyMonkey®. Various parameters such as indications for IHC staining, IHC clones, and IHC staining procedures were questioned. Finally, systematic reporting of non-classical ILC variants were also interrogated. This survey was sent out to pathologists worldwide and circulated from December 14, 2020 until July, 1 2021. The results demonstrate that approximately half of the institutions use E-cadherin expression loss by IHC as an ancillary test to diagnose ILC and that there is a great variability in immunostaining protocols. This might cause different staining results and discordant interpretations. As ILC-specific therapeutic and diagnostic avenues are currently explored in the context of clinical trials, it is of importance to improve standardization of histopathologic diagnosis of ILC diagnosis.
AB - Invasive lobular carcinoma (ILC) represents the second most common subtype of breast cancer (BC), accounting for up to 15% of all invasive BC. Loss of cell adhesion due to functional inactivation of E-cadherin is the hallmark of ILC. Although the current world health organization (WHO) classification for diagnosing ILC requires the recognition of the dispersed or linear non-cohesive growth pattern, it is not mandatory to demonstrate E-cadherin loss by immunohistochemistry (IHC). Recent results of central pathology review of two large randomized clinical trials have demonstrated relative overdiagnosis of ILC, as only ~60% of the locally diagnosed ILCs were confirmed by central pathology. To understand the possible underlying reasons of this discrepancy, we undertook a worldwide survey on the current practice of diagnosing BC as ILC. A survey was drafted by a panel of pathologists and researchers from the European lobular breast cancer consortium (ELBCC) using the online tool SurveyMonkey®. Various parameters such as indications for IHC staining, IHC clones, and IHC staining procedures were questioned. Finally, systematic reporting of non-classical ILC variants were also interrogated. This survey was sent out to pathologists worldwide and circulated from December 14, 2020 until July, 1 2021. The results demonstrate that approximately half of the institutions use E-cadherin expression loss by IHC as an ancillary test to diagnose ILC and that there is a great variability in immunostaining protocols. This might cause different staining results and discordant interpretations. As ILC-specific therapeutic and diagnostic avenues are currently explored in the context of clinical trials, it is of importance to improve standardization of histopathologic diagnosis of ILC diagnosis.
UR - http://www.scopus.com/inward/record.url?scp=85135478390&partnerID=8YFLogxK
U2 - 10.1038/s41379-022-01135-2
DO - 10.1038/s41379-022-01135-2
M3 - Article
C2 - 35922548
AN - SCOPUS:85135478390
SN - 0893-3952
VL - 35
SP - 1812
EP - 1820
JO - Modern Pathology
JF - Modern Pathology
IS - 12
ER -