Back to Search Start Over

A Case Report of Pathologically Complete Response of a Huge Lymph Node Metastasis of Colorectal Cancer After Treatment with Intratumoral Oncolytic Virus H101 and Capecitabine

Authors :
Wang Y
Wang T
Zhang Y
Source :
ImmunoTargets and Therapy, Vol Volume 13, Pp 343-348 (2024)
Publication Year :
2024
Publisher :
Dove Medical Press, 2024.

Abstract

Yaqin Wang, Tianxiao Wang, Yuewei Zhang Hepatobiliary Pancreatic Center Department, Beijing Tsinghua Changgung Hospital Affiliated to Tsinghua University, Beijing, 102218, People’s Republic of ChinaCorrespondence: Yuewei Zhang, Hepatobiliary Pancreatic Center Department, Beijing Tsinghua Changgung Hospital Affiliated to Tsinghua University, Beijing, 102218, People’s Republic of China, Email zywa01618@btch.edu.cnAbstract: Unresectable recurrent lymph node metastasis of colorectal cancer (CRC) is considered as an incurable disease clinically and has a very poor prognosis. Here, we report a male KRAS wild-type CRC case with a huge abdominal lymph node metastasis (12 cm in diameter) after CRC surgery. After three intratumoral injections of oncolytic virus (H101) combined with four cycles of low-dose oral capecitabine, the size of the metastatic lymph node shrank remarkably in response to the anticancer drug and a complete response (CR) was achieved with progression-free survival (PFS) of 19 months. The main adverse reaction was mild fever, which was relieved after physical cooling. The patient is in a general good condition now without any relapse of abdominal lymph node for over a year. On this basis, we propose that the combination therapy of oncolytic virus and capecitabine could be a promising clinical therapeutic strategy for unresectable recurrent lymph node metastasis in CRC patients.Keywords: colorectal cancer, recurrent lymph node metastasis, oncolytic virus, capecitabine

Details

Language :
English
ISSN :
22531556
Volume :
ume 13
Database :
Directory of Open Access Journals
Journal :
ImmunoTargets and Therapy
Publication Type :
Academic Journal
Accession number :
edsdoj.39b4839c9f474b20a8d20ec847132bc1
Document Type :
article