TY - JOUR
T1 - Clinical practice guidance for next-generation sequencing in cancer diagnosis and treatment (edition 2.1)
AU - Japanese Society of Medical Oncology
AU - Japan Society of Clinical Oncology
AU - Japanese Cancer Association
AU - Naito, Yoichi
AU - Aburatani, Hiroyuki
AU - Amano, Toraji
AU - Baba, Eishi
AU - Furukawa, Toru
AU - Hayashida, Tetsu
AU - Hiyama, Eiso
AU - Ikeda, Sadakatsu
AU - Kanai, Masashi
AU - Kato, Motohiro
AU - Kinoshita, Ichiro
AU - Kiyota, Naomi
AU - Kohno, Takashi
AU - Kohsaka, Shinji
AU - Komine, Keigo
AU - Matsumura, Itaru
AU - Miura, Yuji
AU - Nakamura, Yoshiaki
AU - Natsume, Atsushi
AU - Nishio, Kazuto
AU - Oda, Katsutoshi
AU - Oda, Naoyuki
AU - Okita, Natsuko
AU - Oseto, Kumiko
AU - Sunami, Kuniko
AU - Takahashi, Hideaki
AU - Takeda, Masayuki
AU - Tashiro, Shimon
AU - Toyooka, Shinichi
AU - Ueno, Hideki
AU - Yachida, Shinichi
AU - Yoshino, Takayuki
AU - Tsuchihara, Katsuya
N1 - Funding Information:
Yoichi Naito received honoraria from Eisai Co., Ltd., Chugai Pharmaceutical Co., Ltd., Novartis Pharma K.K., and Pfizer Japan Inc., and research funding from AstraZeneca K.K., Eli Lilly Japan K.K., Pfizer Japan Inc., Roche (Ignyta Inc.). Hiroyuki Aburatani received research funding from Chugai Pharmaceutical Co., Ltd., BrightPath Biotherapeutics Co., Ltd., Hitachi Ltd., Fujitsu Ltd., Kyowa Kirin Co., Ltd., and Kowa Co., Ltd.. Eishi Baba received honoraria from Taiho Pharmaceutical Co., Ltd., Chugai Pharmaceutical Co., Ltd., and Eli Lilly Japan K.K., research funding from Mediscience Planning Inc. and MSD K.K., and scholarship donations from Taiho Pharmaceutical Co., Ltd., Chugai Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Merck Biopharma Co., Ltd, Takeda Pharmaceutical Co., Ltd., and Ono Pharmaceutical Co., Ltd. Toru Furukawa received research funding from Tokyo Central Pathology Laboratory Co., Ltd. and Annai Yakkyoku Co., Ltd. Tetsu Hayashida received honoraria from Eisai Co., Ltd., AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., and Novartis Pharma K.K., research funding from Novartis Pharma K.K., Denka Co., Ltd., and Shionogi Co., Ltd., and scholarship donations from Taiho Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd., and Eisai Co., Ltd. Sadakatsu Ikeda received research funding from ACT Genomics Co., Ltd. Masashi Kanai received stock ownership from Therabiopharma Inc. and honoraria from Chugai Pharmaceutical Co., Ltd. Motohiro Kato received research funding from Daiichi Sankyo Co., Ltd. Naomi Kiyota received honoraria from Ono Pharmaceutical Co., Ltd., Bristol-Meyers Squibb K.K., Eisai Co., Ltd., and Bayer Yakuhin Ltd., and research funding from Ono Pharmaceutical Co., Ltd., and Chugai Pharmaceutical Co., Ltd. Takashi Kohno received research funding from Sysmex Corp. Shinji Kohsaka received research funding from AstraZeneca K.K., Nippon Boehringer Ingelheim Co., Ltd., Daiichi Sankyo Co., Ltd. Itaru Matsumura received honoraria from Novartis Pharma K.K., Bristol-Meyers Squibb K.K., Pfizer Japan Inc., Daiichi Sankyo Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Astellas Pharma Inc., Amgen Astellas BioPharma Inc., and research funding from Ono Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., Chugai Pharmaceutical Co., Ltd., Nippon Shinyaku Co., Ltd., Kyowa Kirin Co., Ltd., Sumitomo Dainippon Pharma Co., Ltd., Shionogi Co., Ltd., AbbVie G.K., Asahi Kasei Corp., Eisai Co., Ltd., and Otsuka Pharmaceutical Co., Ltd. Yuji Miura received honoraria from Ono Pharmaceutical Co., Ltd., Bristol-Meyers Squibb K.K., MSD K.K., Chugai Pharmaceutical Co., Ltd., AstraZeneca K.K., and Takeda Pharmaceutical Co., Ltd., and scholarship donations from Taiho Pharmaceutical Co., Ltd., Chugai Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd., Astellas Pharma Inc., Ono Pharmaceutical Co., Ltd., Shionogi Co., Ltd., and Eisai Co., Ltd.. Atsushi Natsume has an employment/leadership position/advisory role of NGK Spark Plug Co., Ltd., and received honoraria from Daiichi Sankyo Co., Ltd., Chugai Pharmaceutical Co., Ltd., Merck Biopharma Co., Ltd, Nippon Kayaku Co., Ltd., and Eisai Co., Ltd. Kazuto Nishio received honoraria from Sumitomo Bakelite Co., Ltd., Daiichi Sankyo Co., Ltd., Nippon Boehringer Ingelheim Co., Ltd., AstraZeneca K.K., Eisai Co., Ltd., and Chugai Pharmaceutical Co., Ltd., fees for promotional materials from Eisai Co., Ltd., and research funding from Korea Otsuka Pharmaceutical Co., Ltd., Life Technologies Japan Ltd., Nippon Boehringer Ingelheim Co., Ltd., Ignyta Inc., and Eli Lilly Japan K.K. Katsutoshi Oda received honoraria from AstraZeneca K.K., and Chugai Pharmaceutical Co Ltd., and research funding from AstraZeneca K.K., and Daiichi Sankyo Co. Ltd. Kumiko Oseto has an employment/leadership position/advisory role of Konica Minolta Precision Medicine Japan, Inc. Shinichi Toyooka received honoraria from Astellas Pharma Inc., Taiho Pharmaceutical Co. Ltd., and Eisai Co., Ltd., and research funding from Mitsui E&S Holding Co. Ltd., Eufofins Clinical Genetics Co., Ltd., Daiichi Sankyo Co. Ltd., Yamada Bee Company, Inc., and SBI Life Insurance Co. Ltd. Takayuki Yoshino received honoraria from Taiho Pharmaceutical Co., Ltd., Chugai Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Sanofi K.K., Takeda Pharmaceutical Co., Ltd., and Merck Biopharma Co., Ltd, and research funding from MSD K.K., Ono Pharmaceutical Co., Ltd., GlaxoSmithKline K.K., Sanofi K.K., Daiichi Sankyo Co., Ltd., Sumitomo Dainippon Pharma Co., Ltd., Chugai Pharmaceutical Co., Ltd., and Parexel International Inc. Other authors have no conflict of interest.
Funding Information:
This work was supported by the Japanese Society of Medical Oncology (JSMO), the Japan Society of Clinical Oncology (JSCO), and the Japanese Cancer Association (JCA). The JSMO and JSCO, and JCA Guideline Committee members reviewed the guidance. This project was supported by Health Labour Sciences Special Research Grant (19EA1001).
Publisher Copyright:
© 2020, The Author(s).
PY - 2021/2
Y1 - 2021/2
N2 - Background: To promote precision oncology in clinical practice, the Japanese Society of Medical Oncology, the Japanese Society of Clinical Oncology, and the Japanese Cancer Association, jointly published “Clinical practice guidance for next-generation sequencing in cancer diagnosis and treatment” in 2017. Since new information on cancer genomic medicine has emerged since the 1st edition of the guidance was released, including reimbursement for NGS-based multiplex gene panel tests in 2019, the guidance revision was made. Methods: A working group was organized with 33 researchers from cancer genomic medicine designated core hospitals and other academic institutions. For an impartial evaluation of the draft version, eight committee members from each society conducted an external evaluation. Public comments were also made on the draft. The finalized Japanese version was published on the websites of the three societies in March 2020. Results: The revised edition consists of two parts: an explanation of the cancer genomic profiling test (General Discussion) and clinical questions (CQs) that are of concern in clinical practice. Particularly, patient selection should be based on the expectation that the patient's post-test general condition and organ function will be able to tolerate drug therapy, and the optimal timing of test should be considered in consideration of subsequent treatment plans, not limited to treatment lines. Conclusion: We expect that the revised version will be used by healthcare professionals and will also need to be continually reviewed in line with future developments in cancer genome medicine.
AB - Background: To promote precision oncology in clinical practice, the Japanese Society of Medical Oncology, the Japanese Society of Clinical Oncology, and the Japanese Cancer Association, jointly published “Clinical practice guidance for next-generation sequencing in cancer diagnosis and treatment” in 2017. Since new information on cancer genomic medicine has emerged since the 1st edition of the guidance was released, including reimbursement for NGS-based multiplex gene panel tests in 2019, the guidance revision was made. Methods: A working group was organized with 33 researchers from cancer genomic medicine designated core hospitals and other academic institutions. For an impartial evaluation of the draft version, eight committee members from each society conducted an external evaluation. Public comments were also made on the draft. The finalized Japanese version was published on the websites of the three societies in March 2020. Results: The revised edition consists of two parts: an explanation of the cancer genomic profiling test (General Discussion) and clinical questions (CQs) that are of concern in clinical practice. Particularly, patient selection should be based on the expectation that the patient's post-test general condition and organ function will be able to tolerate drug therapy, and the optimal timing of test should be considered in consideration of subsequent treatment plans, not limited to treatment lines. Conclusion: We expect that the revised version will be used by healthcare professionals and will also need to be continually reviewed in line with future developments in cancer genome medicine.
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U2 - 10.1007/s10147-020-01831-6
DO - 10.1007/s10147-020-01831-6
M3 - Article
C2 - 33249514
AN - SCOPUS:85096825185
SN - 1341-9625
VL - 26
SP - 233
EP - 283
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 2
ER -