Japanese Society of Medical Oncology clinical guidelines: Molecular testing for colorectal cancer treatment, 5th edition

Author:

Bando Hideaki1ORCID,Yamaguchi Kyoko2,Mitani Seiichiro3,Sawada Kentaro4,Mishima Saori1ORCID,Komine Keigo5,Okugawa Yoshinaga6,Hosoda Waki7ORCID,Ebi Hiromichi89ORCID

Affiliation:

1. Department of Gastroenterology and Gastrointestinal Oncology National Cancer Center Hospital East Chiba Japan

2. Department of Hematology, Oncology, and Cardiovascular Medicine Kyushu University Hospital Fukuoka Japan

3. Department of Medical Oncology Kindai University Faculty of Medicine Osaka‐Sayama Japan

4. Department of Clinical Oncology Kushiro Rosai Hospital Kushiro Japan

5. Department of Medical Oncology Tohoku University Hospital Sendai Japan

6. Department of Genomic Medicine Mie University Faculty of Medicine Tsu Japan

7. Department of Molecular Diagnostics Aichi Cancer Center Nagoya Japan

8. Division of Molecular Therapeutics Aichi Cancer Center Research Institute Nagoya Japan

9. Division of Advanced Cancer Therapeutics Nagoya University Graduate School of Medicine Nagoya Japan

Abstract

AbstractMolecular testing to determine optimal therapies is essential for managing patients with colorectal cancer (CRC). In October 2022, the Japanese Society of Medical Oncology published the 5th edition of the Molecular Testing Guideline for Colorectal Cancer Treatment. In this guideline, in patients with unresectable CRC, RAS/BRAF V600E mutational and mismatch repair tests are strongly recommended prior to first‐line chemotherapy to select optimal first‐ and second‐line therapies. In addition, HER2 testing is strongly recommended because the pertuzumab plus trastuzumab combination is insured after fluoropyrimidine, oxaliplatin, and irinotecan in Japan. Circulating tumor DNA (ctDNA)‐based RAS testing is also strongly recommended to assess the indications for the readministration of anti‐EGFR antibodies. Both tissue‐ and ctDNA‐based comprehensive genomic profiling tests are strongly recommended to assess the indications for targeted molecular drugs, although they are currently insured in patients with disease progression after receiving standard chemotherapy (or in whom disease progression is expected in the near future). Mutational and mismatch repair testing is strongly recommended for patients with resectable CRC, and RAS/BRAF V600E mutation testing is recommended to estimate the risk of recurrence. Mutational and mismatch repair and BRAF testing are also strongly recommended for screening for Lynch syndrome. Circulating tumor DNA‐based minimal residual disease (MRD) testing is strongly recommended for estimating the risk of recurrence based on clinical evidence, although MRD testing was not approved in Japan at the time of the publication of this guideline.

Funder

Japanese Society of Medical Oncology

Publisher

Wiley

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