TY - JOUR
T1 - Japan society of clinical oncology/Japanese society of medical oncology-led clinical recommendations on the diagnosis and use of tropomyosin receptor kinase inhibitors in adult and pediatric patients with neurotrophic receptor tyrosine kinase fusion-positive advanced solid tumors, cooperated by the Japanese society of pediatric hematology/oncology
AU - Naito, Yoichi
AU - Mishima, Saori
AU - Akagi, Kiwamu
AU - Igarashi, Ataru
AU - Ikeda, Masafumi
AU - Okano, Susumu
AU - Kato, Shunsuke
AU - Takano, Tadao
AU - Tsuchihara, Katsuya
AU - Terashima, Keita
AU - Nishihara, Hiroshi
AU - Nishiyama, Hiroyki
AU - Hiyama, Eiso
AU - Hirasawa, Akira
AU - Hosoi, Hajime
AU - Maeda, Osamu
AU - Yatabe, Yasushi
AU - Okamoto, Wataru
AU - Ono, Shigeru
AU - Kajiyama, Hiroaki
AU - Nagashima, Fumio
AU - Hatanaka, Yutaka
AU - Miyachi, Mitsuru
AU - Kodera, Yasuhiro
AU - Yoshino, Takayuki
AU - Taniguchi, Hiroya
N1 - Funding Information:
This guideline was led by Japan Society of Clinical Oncology (JSCO)/Japanese Society of Medical Oncology (JSMO) collaboration, cooperated by The Japanese Society of Pediatric Hematology/Oncology (JSPHO). The authors would like to thank Prof. Y. Kitagawa, the president of JSCO, Mr. S. Akimoto, and Mr. Y. Yamamoto as the JSCO secretariat for their on-site assistance. The authors would like to thank Prof. Y. Ishioka, the president of JSMO, Mr. D. Kawashima, and Ms. H. Nishizawa as the secretariat of JSMO for their on-site assistance. The authors would like to thank Prof. H. Hosoi, the president of JSPHO for support. The authors would like to thank BIC (www.bic.co.jp) for the English language review.
Funding Information:
This guideline was supported by following funds: JSCO and JSMO Funds, including the Ministry of Health, Labour, and Welfare General Research Enterprise for Promoting Cancer Measures”Improvement in the quality of systems for providing medical treatment through the creation of guidelines for diagnosing rare forms of cancer” (Research Representative—Yasuhiro Kodera, (H29 -measures against cancers- public-013). Acknowledgements
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/3/1
Y1 - 2020/3/1
N2 - Background: The development of novel antitumor agents and accompanying biomarkers has improved survival across several tumor types. Previously, we published provisional clinical opinion for the diagnosis and use of immunotherapy in patients with deficient DNA mismatch repair tumors. Recently, efficacy of tropomyosin receptor kinase inhibitors against neurotrophic receptor tyrosine kinase (NTRK) fusion gene-positive advanced solid tumors have been established as the second tumor-agnostic treatment, making it necessary to develop the guideline prioritized for these patients. Methods: Clinical questions regarding medical care were formulated for patients with NTRK-positive advanced solid tumors. Relevant publications were searched by PubMed and Cochrane Database. Critical publications and conference reports were added manually. Systematic reviews were performed for each clinical question for the purpose of developing clinical recommendations. The committee members identified by Japan Society of Clinical Oncology (JSCO) and Japanese Society of Medical Oncology (JSMO) voted to determine the level of each recommendation considering the strength of evidence, expected risks and benefits to patients, and other related factors. Thereafter, a peer review by experts nominated from JSCO, JSMO, and Japanese Society of Pediatric Hematology/Oncology, and the public comments among all Societies’ members was done. Results: The current guideline describes 3 clinical questions and 15 recommendations for whom, when, and how NTRK fusion should be tested, and what is recommended for patients with NTRK fusion-positive advanced solid tumors. Conclusion: In the NTRK guideline, the committee proposed 15 recommendations for performing NTRK testing properly to select patients who are likely to benefit from tropomyosin receptor kinase inhibitors.
AB - Background: The development of novel antitumor agents and accompanying biomarkers has improved survival across several tumor types. Previously, we published provisional clinical opinion for the diagnosis and use of immunotherapy in patients with deficient DNA mismatch repair tumors. Recently, efficacy of tropomyosin receptor kinase inhibitors against neurotrophic receptor tyrosine kinase (NTRK) fusion gene-positive advanced solid tumors have been established as the second tumor-agnostic treatment, making it necessary to develop the guideline prioritized for these patients. Methods: Clinical questions regarding medical care were formulated for patients with NTRK-positive advanced solid tumors. Relevant publications were searched by PubMed and Cochrane Database. Critical publications and conference reports were added manually. Systematic reviews were performed for each clinical question for the purpose of developing clinical recommendations. The committee members identified by Japan Society of Clinical Oncology (JSCO) and Japanese Society of Medical Oncology (JSMO) voted to determine the level of each recommendation considering the strength of evidence, expected risks and benefits to patients, and other related factors. Thereafter, a peer review by experts nominated from JSCO, JSMO, and Japanese Society of Pediatric Hematology/Oncology, and the public comments among all Societies’ members was done. Results: The current guideline describes 3 clinical questions and 15 recommendations for whom, when, and how NTRK fusion should be tested, and what is recommended for patients with NTRK fusion-positive advanced solid tumors. Conclusion: In the NTRK guideline, the committee proposed 15 recommendations for performing NTRK testing properly to select patients who are likely to benefit from tropomyosin receptor kinase inhibitors.
KW - Advanced solid tumor
KW - Clinical practice guideline
KW - Neurotrophic receptor tyrosine kinase (NTRK) fusion
KW - Tropomyosin receptor kinase (TRK) inhibitor
KW - Tumor-agnostic treatment
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U2 - 10.1007/s10147-019-01610-y
DO - 10.1007/s10147-019-01610-y
M3 - Article
C2 - 31974683
AN - SCOPUS:85078331217
SN - 1341-9625
VL - 25
SP - 403
EP - 417
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 3
ER -