Histopathological atlas of desmoplastic reaction characterization in colorectal cancer

Author:

Ueno Hideki1,Kajiwara Yoshiki1,Ajioka Yoich2,Sugai Tamotsu3,Sekine Shigeki4,Ishiguro Megumi5,Takashima Atsuo6,Kanemitsu Yukihide7

Affiliation:

1. Department of Surgery, National Defense Medical College, Saitama, Japan

2. Division of Molecular and Diagnostic Pathology, Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan

3. Department of Molecular Diagnostic Pathology, School of Medicine, Iwate Medical University, Iwate, Japan

4. Division of Pathology and Clinical Laboratories, National Cancer Center Hospital, Tokyo, Japan

5. Department of Translational Oncology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan

6. Gastrointestinal Medical Oncology Division, National Cancer Center Hospital, Tokyo, Japan

7. Department of Colorectal Surgery, National Cancer Center Hospital, Tokyo, Japan

Abstract

Abstract Emergent scientific evidence indicates the central role of cancer-associated fibroblasts in determining whether the microenvironment of cancer works as friend or foe of the host; however, there is no unified histological evaluation framework of fibrotic stroma in colorectal cancers. Myxoid stroma and keloid-like collagen are site-specific histopathological features generated by cancer-associated fibroblasts, which appear exclusively in the tumor front during desmoplastic reaction. On the basis of these two stromal components, desmoplastic reaction is categorized into three patterns—immature, intermediate and mature—using hematoxylin and eosin staining. In January 2020, a prospective randomized clinical trial, JCOG1805, to elucidate the value of adjuvant chemotherapy in stage II colorectal cancer patients with pathological risk factors of recurrence was launched in Japan, in which intermediate/immature desmoplastic reaction is one of the four risk factors selected as inclusion criteria. This paper covers the diagnostic criteria for the desmoplastic reaction classification being used in the JCOG1805 study.

Funder

Japan Agency for Medical Research and Development

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology,General Medicine

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