Retrospective multicenter study for assessment of association between imaging change and outcome after treatment of regorafenib: KSCC1603.

Authors

null

Taito Esaki

Department of Gastrointestinal and Medical Oncology, National Kyushu Cancer Center, Fukuoka, Japan

Taito Esaki , Masahiro Kawahira , Tetsuya Kusumoto , Satoshi Yuki , Kazuteru Hatanaka , Yoshimitsu Kobayashi , Akihiro Nishie , Satoshi Kawanami , Akitaka Makiyama , Hiroshi Saeki , Mototsugu Shimokawa , Eiji Oki , Yoshihiko Maehara

Organizations

Department of Gastrointestinal and Medical Oncology, National Kyushu Cancer Center, Fukuoka, Japan, Shizuoka General Hospital Cancer Center, Shizuoka, Japan, Department of Gastroenterological Surgery and Clinical Research Institute Cancer Research Division, National Kyushu Medical Center, Fukuoka, Japan, Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan, Hakodate Municipal Hospital, Hakodate, Japan, Hokkaido University Hospital, Sapporo, Japan, Department of Clinical Radiology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan, Department of Hematology/Oncology, Japan Community Health Care Organization Kyushu Hospital, Kitakyushu, Japan, Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan, Clinical Research Institute, National Kyushu Cancer Center, Fukuoka, Japan, Department of Surgery and Science, Kyushu University, Fukuoka, Japan, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan

Research Funding

Pharmaceutical/Biotech Company

Background: Molecular-targeted drugs are known to have angiogenesis-inhibiting properties, and thus can inhibit angiogenesis inside the tumor tissue to cause necrosis, even if the tumor diameter is unchanged. We retrospectively investigated relationship between imaging change associated with regorafenib (REGO) treatment and the treatment outcome in Japanese mCRC. Methods: Eligibility included ECOG-PS 0 or 1, treated with REGO with lung or liver metastasis, started dose with 120 or 160mg/day of regorafenib and duration of treatment (DOT) must be 35 days or more (excluding interruption). Patients (Pts) were performed baseline CT within 28 days before and first CT assessment were between eight and 12 weeks after start of regorafenib. The main objective of this analysis is to investigate the correlation between the imaging change and outcome. As imaging change, onset or increase of Cavitation of lung lesion (CLL), morphologic response of liver lesion (MRL), Change of liver metastasis density (CLD) were evaluated. In all cases, independent two radiologists are evaluating radiological change after regorafenib treatment. Results: We finally screened 671 cases and 231 cases were eligible. The pts background was male/female 147/84, median age 64.0 (range: 32-83), median DOT of REGO 86 days (range: 35-818). The pts with lung metastasis were 153, and with liver metastasis were 166. CLL were positive in 69 (40.0%) pts. The median progression free survival (PFS) of the pts with/without CLL were 3.2/2.4 months (HR 0.794; 95% CI 0.584-1.080). Median overall survival (OS) of the pts with/without CLL were 10.5/9.0 months (HR 1.058; 95% CI 0.751-1.489). Median OS of pts with/without CLL in female were 11.4/7.9 months (HR 0.630; 95% CI 0.352-1.127). The MRL and CLD of liver metastasis were analyzed in 147 / 91 pt. Median OS of pts with/without MRL were 9.9/8.2 months (HR 1.015; 95% CI 0.581-1.774) and Median OS with/ without CLD were 11.6/7.0 months (HR 0.604; 95% CI 0.353-1.031). Conclusions: Cavitation of lung metastasis may predict PFS of the pts but not OS. Change of Liver metastasis density were predictor of favorable outcome to regorafenib. (UMIN000023329).

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2019 Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Cancers of the Colon, Rectum, and Anus

Track

Cancers of the Colon, Rectum, and Anus

Sub Track

Prevention, Diagnosis, and Screening

Citation

J Clin Oncol 37, 2019 (suppl 4; abstr 509)

DOI

10.1200/JCO.2019.37.4_suppl.509

Abstract #

509

Poster Bd #

D12

Abstract Disclosures

Similar Abstracts

First Author: Xiang Gao

Abstract

2022 ASCO Annual Meeting

Automated detection and segmentation of small cell lung cancer liver metastases on CT.

First Author: Usamah Chaudhary

First Author: Jude Khatib