Outcome of Mismatch Repair-Deficient Metastatic Colorectal Cancer: The Mayo Clinic Experience

被引:34
|
作者
Jin, Zhaohui [1 ]
Sanhueza, Cristobal T. [1 ]
Johnson, Benny [1 ]
Nagorney, David M. [2 ]
Larson, David W. [2 ]
Mara, Kristin C. [3 ]
Harmsen, William C. [3 ]
Smyrk, Thomas C. [4 ]
Grothey, Axel [1 ]
Hubbard, Joleen M. [1 ]
机构
[1] Mayo Clin & Mayo Fdn, Dept Med Oncol, 200 First St SW, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Surg, 200 1st St SW, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Stat, 200 1st St SW, Rochester, MN 55905 USA
[4] Mayo Clin & Mayo Fdn, Dept Pathol, Rochester, MN 55905 USA
来源
ONCOLOGIST | 2018年 / 23卷 / 09期
关键词
High microsatellite instability; Metastatic colorectal cancer; Metastasectomy; Microsatellite-stable; MICROSATELLITE-INSTABILITY; COLON-CANCER; LYNCH-SYNDROME; BRAF MUTATION; FAMILIAL PREDISPOSITION; INTERNATIONAL CRITERIA; INSTITUTE WORKSHOP; ADJUVANT THERAPY; RECTAL-CANCER; PROGNOSIS;
D O I
10.1634/theoncologist.2017-0289
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Deficiencies in the DNA mismatch repair system cause errors during DNA replication, which in turn give rise to microsatellite instability (MSI). The impact of MSI on survival in metastatic colorectal cancer (mCRC) is unclear. This cohort study aims to investigate the prognostic and predictive value of MSI in mCRC prior to the immune therapy era. Materials and Methods. A total of 75 MSI-high (MSI-H) mCRC patients (pts) and 75 matched (age, gender, disease sidedness, metachronous/synchronous) microsatellite-stable (MSS) mCRC pts were identified from 1,268 mCRC pts who had MSI/mismatch repair test results at Mayo Clinic Rochester between January 1992 and July 2016. A retrospective review was conducted by using data from electronic medical records. Statistical analyses utilized the Kaplan-Meier method, log-rank test, and Cox proportional hazards models. Results. The MSS group was well matched to the MSI-H group based on age, gender, location, and chronicity of metastatic disease. MSI-H mCRC pts had earlier disease recurrence (median time from initial diagnosis to metastatic disease diagnosis, MSI-H group 12.9 vs. MSS group 20.9 months, p=.034). Median overall survival (OS) was 28.1 and 37.4 months for MSI-H and MSS pts, respectively (p=.99). In total, 94.7% of MSI-H pts and 98.7% of MSS pts had fluoropyrimidine-based chemotherapy for metastatic disease, and there was no difference in OS between these two groups (32.3 vs. 37.4 months, p=.91). Forty-three MSI-H and thirty-nine MSS pts had metastasectomy and/or ablation of metastases (p=.51) with longer median OS compared with pts without metastasectomy (MSI-H: 82.0 vs. 13.9, p < .001; MSS: 69.9 vs. 19.7, p<.001). Age <65 years, BRAF wild type, and metastasectomy were associated with better OS in univariate analysis. Only metastasectomy remained statistically significant in multivariate analysis (p<.001). Conclusion. In mCRC, patients with MSI-H tumors have similar, but numerically shorter, median overall survival compared with those with MSS tumors. In both groups, metastasectomy and ablation of metastatic disease should be considered to optimize OS.
引用
收藏
页码:1083 / 1091
页数:9
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