Microsatellite instability and its associations with the clinicopathologic characteristics of diffuse large B‐cell lymphoma

Abstract Microsatellite instability (MSI) has been investigated as a prognostic and predictive factor for chemotherapy in colorectal cancer and has recently been demonstrated to be predictive of the PD‐1/PD‐L1 checkpoint blockade response in various solid tumors. However, MSI status in diffuse large...

Full description

Bibliographic Details
Main Authors: Tian Tian, Jiwei Li, Tian Xue, Baohua Yu, Xiaoqiu Li, Xiaoyan Zhou
Format: Article
Language:English
Published: Wiley 2020-04-01
Series:Cancer Medicine
Subjects:
MSI
Online Access:https://doi.org/10.1002/cam4.2870
id doaj-a7953b5a55ed4d9a998219034e01dcd3
record_format Article
spelling doaj-a7953b5a55ed4d9a998219034e01dcd32020-11-25T02:29:03ZengWileyCancer Medicine2045-76342020-04-01972330234210.1002/cam4.2870Microsatellite instability and its associations with the clinicopathologic characteristics of diffuse large B‐cell lymphomaTian Tian0Jiwei Li1Tian Xue2Baohua Yu3Xiaoqiu Li4Xiaoyan Zhou5Department of Pathology Fudan University Shanghai Cancer Center Shanghai ChinaDepartment of Pathology Fudan University Shanghai Cancer Center Shanghai ChinaDepartment of Pathology Fudan University Shanghai Cancer Center Shanghai ChinaDepartment of Pathology Fudan University Shanghai Cancer Center Shanghai ChinaDepartment of Pathology Fudan University Shanghai Cancer Center Shanghai ChinaDepartment of Pathology Fudan University Shanghai Cancer Center Shanghai ChinaAbstract Microsatellite instability (MSI) has been investigated as a prognostic and predictive factor for chemotherapy in colorectal cancer and has recently been demonstrated to be predictive of the PD‐1/PD‐L1 checkpoint blockade response in various solid tumors. However, MSI status in diffuse large B‐cell lymphomas (DLBCLs) has not been thoroughly explored. This study investigated MSI status in DLBCLs and analyzed the associations between MSI and clinicopathologic characteristics and clinical outcomes. Ninety‐two cases of primary DLBCLs treated with R‐CHOP/CHOP chemotherapy between 2009 and 2017 were collected. MSI detection was performed by the Promega MSI Analysis System. The protein expression of MLH1, MSH2, MSH6, and PMS2 was detected by immunohistochemistry. The associations of MSI‐H and MSI‐L with progression‐free survival (PFS) and overall survival (OS) were assessed by COX models and Kaplan–Meier curves. The correlations of complete response (CR) after R‐CHOP/CHOP chemotherapy with MSI‐H and MSI‐L were examined by univariate and multivariate logistic regression analyses, respectively. 3 of 92 cases (3.2%) were high MSI (MSI‐H), and 9 cases (9/92, 9.8%) exhibited low MSI (MSI‐L). One case with MSI‐H showed negative expression of MSH2 and MSH6. Univariate analysis indicated that MSI‐L was correlated with poor response to R‐CHOP/CHOP chemotherapy in DLBCLs (OR, 0.178; 95% CI, 0.041‐0.776; P = .022). Multivariate analysis showed that MSI‐L was an independent predictive factor for non‐CR to R‐CHOP/CHOP chemotherapy (OR, 0.144; 95% CI, 0.027‐0.761; P = .023). Kaplan‐Meier curves showed that there was a trend that MSI‐H patients had favorable PFS (P = .36) and OS (P = .48), which did not have statistical significance and MSI‐L was not significantly correlated with PFS (P = .24) and OS (P = .52).Our study indicated that there existed MSI‐H and MSI‐L in DLBCLs. MSI‐L could be an independent predictive factor for the chemotherapy response in DLBCLs.https://doi.org/10.1002/cam4.2870chemotherapy responsecomplete responseDLBCLsMSI
collection DOAJ
language English
format Article
sources DOAJ
author Tian Tian
Jiwei Li
Tian Xue
Baohua Yu
Xiaoqiu Li
Xiaoyan Zhou
spellingShingle Tian Tian
Jiwei Li
Tian Xue
Baohua Yu
Xiaoqiu Li
Xiaoyan Zhou
Microsatellite instability and its associations with the clinicopathologic characteristics of diffuse large B‐cell lymphoma
Cancer Medicine
chemotherapy response
complete response
DLBCLs
MSI
author_facet Tian Tian
Jiwei Li
Tian Xue
Baohua Yu
Xiaoqiu Li
Xiaoyan Zhou
author_sort Tian Tian
title Microsatellite instability and its associations with the clinicopathologic characteristics of diffuse large B‐cell lymphoma
title_short Microsatellite instability and its associations with the clinicopathologic characteristics of diffuse large B‐cell lymphoma
title_full Microsatellite instability and its associations with the clinicopathologic characteristics of diffuse large B‐cell lymphoma
title_fullStr Microsatellite instability and its associations with the clinicopathologic characteristics of diffuse large B‐cell lymphoma
title_full_unstemmed Microsatellite instability and its associations with the clinicopathologic characteristics of diffuse large B‐cell lymphoma
title_sort microsatellite instability and its associations with the clinicopathologic characteristics of diffuse large b‐cell lymphoma
publisher Wiley
series Cancer Medicine
issn 2045-7634
publishDate 2020-04-01
description Abstract Microsatellite instability (MSI) has been investigated as a prognostic and predictive factor for chemotherapy in colorectal cancer and has recently been demonstrated to be predictive of the PD‐1/PD‐L1 checkpoint blockade response in various solid tumors. However, MSI status in diffuse large B‐cell lymphomas (DLBCLs) has not been thoroughly explored. This study investigated MSI status in DLBCLs and analyzed the associations between MSI and clinicopathologic characteristics and clinical outcomes. Ninety‐two cases of primary DLBCLs treated with R‐CHOP/CHOP chemotherapy between 2009 and 2017 were collected. MSI detection was performed by the Promega MSI Analysis System. The protein expression of MLH1, MSH2, MSH6, and PMS2 was detected by immunohistochemistry. The associations of MSI‐H and MSI‐L with progression‐free survival (PFS) and overall survival (OS) were assessed by COX models and Kaplan–Meier curves. The correlations of complete response (CR) after R‐CHOP/CHOP chemotherapy with MSI‐H and MSI‐L were examined by univariate and multivariate logistic regression analyses, respectively. 3 of 92 cases (3.2%) were high MSI (MSI‐H), and 9 cases (9/92, 9.8%) exhibited low MSI (MSI‐L). One case with MSI‐H showed negative expression of MSH2 and MSH6. Univariate analysis indicated that MSI‐L was correlated with poor response to R‐CHOP/CHOP chemotherapy in DLBCLs (OR, 0.178; 95% CI, 0.041‐0.776; P = .022). Multivariate analysis showed that MSI‐L was an independent predictive factor for non‐CR to R‐CHOP/CHOP chemotherapy (OR, 0.144; 95% CI, 0.027‐0.761; P = .023). Kaplan‐Meier curves showed that there was a trend that MSI‐H patients had favorable PFS (P = .36) and OS (P = .48), which did not have statistical significance and MSI‐L was not significantly correlated with PFS (P = .24) and OS (P = .52).Our study indicated that there existed MSI‐H and MSI‐L in DLBCLs. MSI‐L could be an independent predictive factor for the chemotherapy response in DLBCLs.
topic chemotherapy response
complete response
DLBCLs
MSI
url https://doi.org/10.1002/cam4.2870
work_keys_str_mv AT tiantian microsatelliteinstabilityanditsassociationswiththeclinicopathologiccharacteristicsofdiffuselargebcelllymphoma
AT jiweili microsatelliteinstabilityanditsassociationswiththeclinicopathologiccharacteristicsofdiffuselargebcelllymphoma
AT tianxue microsatelliteinstabilityanditsassociationswiththeclinicopathologiccharacteristicsofdiffuselargebcelllymphoma
AT baohuayu microsatelliteinstabilityanditsassociationswiththeclinicopathologiccharacteristicsofdiffuselargebcelllymphoma
AT xiaoqiuli microsatelliteinstabilityanditsassociationswiththeclinicopathologiccharacteristicsofdiffuselargebcelllymphoma
AT xiaoyanzhou microsatelliteinstabilityanditsassociationswiththeclinicopathologiccharacteristicsofdiffuselargebcelllymphoma
_version_ 1724834717751050240