Mismatch Repair and Microsatellite Instability Testing for Immune Checkpoint Inhibitor Therapy Guideline From the College of American Pathologists in Collaboration With the Association for Molecular Pathology and Fight Colorectal Cancer

被引:84
作者
Bartley, Angela N. [1 ]
Mills, Anne M. [2 ]
Konnick, Eric [3 ]
Overman, Michael [4 ]
Ventura, Christina B. [5 ]
Souter, Lesley
Colasacco, Carol [5 ]
Stadler, Zsofia K. [6 ]
Kerr, Sarah [7 ]
Howitt, Brooke E. [8 ]
Hampel, Heather [9 ]
Adams, Sarah F. [10 ]
Johnson, Wenora [11 ]
Magi-Galluzzi, Cristina [12 ]
Sepulveda, Antonia R. [13 ]
Broaddus, Russell R. [14 ,15 ]
机构
[1] St Joseph Mercy Hosp, Dept Pathol, Ann Arbor, MI USA
[2] Univ Virginia, Dept Pathol, Charlottesville, VA USA
[3] Univ Washington, Dept Lab Med & Pathol, Seattle, WA USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX USA
[5] Coll Amer Pathologists, Surveys, Northfield, IL USA
[6] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY USA
[7] Hosp Pathol Associates, Minneapolis, MN USA
[8] Stanford Univ, Dept Pathol, Stanford, CA USA
[9] Ohio State Univ, Dept Internal Med, Columbus, OH USA
[10] Univ New Mexico, Dept Obstet & Gynecol, Albuquerque, NM USA
[11] Fight Colorectal Canc, Springfield, MO USA
[12] Univ Alabama, Dept Pathol, Birmingham, England
[13] George Washington Univ, Dept Pathol, Washington, DC USA
[14] Univ N Carolina, Dept Pathol & Lab Med, Sch Med, Chapel Hill, NC USA
[15] Univ N Carolina, Sch Med, Dept Pathol & Lab Med, 308 Brinkhous Bullitt Bldg CB 7525, Chapel Hill, NC 27599 USA
关键词
TUMOR MUTATIONAL BURDEN; LYNCH-SYNDROME; ENDOMETRIAL CANCER; PROTEIN EXPRESSION; IMMUNOHISTOCHEMISTRY; METHYLATION; DEFICIENCY; IDENTIFICATION; HYPERMETHYLATION; IRINOTECAN;
D O I
10.5858/arpa.2021-0632-CP
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Context.-The US Food and Drug Administration (FDA) approved immune checkpoint inhibitor therapy for pa-tients with advanced solid tumors that have DNA mismatch repair defects or high levels of microsatellite instability; however, the FDA provided no guidance on which specific clinical assays should be used to determine mismatch repair status.Objective.-To develop an evidence-based guideline to identify the optimal clinical laboratory test to identify defects in DNA mismatch repair in patients with solid tumor malignancies who are being considered for immune checkpoint inhibitor therapy.Design.-The College of American Pathologists con-vened an expert panel to perform a systematic review of the literature and develop recommendations. Using the National Academy of Medicine-endorsed Grading of Recommendations Assessment, Development and Evalua-tion approach, the recommendations were derived from available evidence, strength of that evidence, open comment feedback, and expert panel consensus. Mismatch repair immunohistochemistry, microsatellite instability derived from both polymerase chain reaction and next -generation sequencing, and tumor mutation burden derived from large panel next-generation sequencing were within scope.Results.-Six recommendations and 3 good practice statements were developed. More evidence and evidence of higher quality were identified for colorectal cancer and other cancers of the gastrointestinal (GI) tract than for cancers arising outside the GI tract.Conclusions.-An optimal assay depends on cancer type. For most cancer types outside of the GI tract and the endometrium, there was insufficient published evidence to recommend a specific clinical assay. Absent published evidence, immunohistochemistry is an acceptable ap-proach readily available in most clinical laboratories.
引用
收藏
页码:1194 / 1210
页数:17
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