Recommendations on Surveillance and Management of Biallelic Mismatch Repair Deficiency (BMMRD) Syndrome: A Consensus Statement by the US Multi-society Task Force on Colorectal Cancer

被引:6
作者
Durno, Carol [1 ]
Boland, C. Richard [2 ]
Cohen, Shlomi [3 ]
Dominitz, Jason A. [4 ,5 ]
Giardiello, Frank M. [6 ]
Johnson, David A. [7 ]
Kaltenbach, Tonya [8 ]
Levin, T. R. [9 ]
Lieberman, David [10 ]
Robertson, Douglas J. [11 ,12 ]
Rex, Douglas K. [13 ]
机构
[1] Univ Toronto, Hosp Sick Children, Zane Cohen Ctr, Mt Sinai Hosp,Div Gastroenterol Hepatol & Nutr,De, Toronto, ON, Canada
[2] Univ Calif San Diego, Dept Med Gastroenterol, San Diego, CA 92103 USA
[3] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Sackler Fac Med, Pediat Gastroenterol Unit,Dana Dwek Childrens Hos, Tel Aviv, Israel
[4] VA Puget Sound Hlth Care Syst, Seattle, WA USA
[5] Univ Washington, Sch Med, Seattle, WA USA
[6] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[7] Eastern Virginia Med Sch, Norfolk, VA 23501 USA
[8] Stanford Univ, Sch Med, Vet Affairs Palo Alto, Palo Alto, CA 94304 USA
[9] Kaiser Permanente Med Ctr, Walnut Creek, CA USA
[10] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[11] VA Med Ctr, White River Jct, VT USA
[12] Geisel Sch Med Dartmouth, Hanover, NH USA
[13] Indiana Univ Sch Med, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
colorectal cancer; Lynch syndrome; biallelic mismatch repair deficiency; BMMRD; constitutional mismatch repair deficiency; CMMRD; cancer; DNA mismatch repair; childhood cancer; EUROPEAN CONSORTIUM CARE; URINARY-TRACT CANCER; LYNCH SYNDROME; MICROSATELLITE INSTABILITY; CORPUS-CALLOSUM; PMS2; MUTATIONS; YOUNG-PATIENTS; FOLLOW-UP; HEREDITARY; GUIDELINES;
D O I
10.1097/MPG.0000000000001578
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The US Multi-Society Task Force on Colorectal Cancer, with invited experts, developed a consensus statement and recommendations to assist health care providers with appropriate management of patients with biallelic mismatch repair deficiency (BMMRD) syndrome, also called constitutional mismatch repair deficiency syndrome. This position paper outlines what is known about BMMRD, the unique genetic and clinical aspects of the disease, and reviews the current management approaches to this disorder. This article represents a starting point from which diagnostic and management decisions can undergo rigorous testing for efficacy. There is a lack of strong evidence and a requirement for further research. Nevertheless, providers need direction on how to recognize and care for BMMRD patients today. In addition to identifying areas of research, this article provides guidance for surveillance and management. The major challenge is that BMMRD is rare, limiting the ability to accumulate unbiased data and develop controlled prospective trials. The formation of effective international consortia that collaborate and share data is proposed to accelerate our understanding of this disease.
引用
收藏
页码:836 / 843
页数:8
相关论文
共 58 条
[51]   Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D) [J].
Vasen, H. F. A. ;
Ghorbanoghli, Z. ;
Bourdeaut, F. ;
Cabaret, O. ;
Caron, O. ;
Duval, A. ;
Entz-Werle, N. ;
Goldberg, Y. ;
Ilencikova, D. ;
Kratz, C. P. ;
Lavoine, N. ;
Loeffen, J. ;
Menko, F. H. ;
Muleris, M. ;
Sebille, G. ;
Colas, C. ;
Burkhardt, B. ;
Brugieres, L. ;
Wimmer, K. .
JOURNAL OF MEDICAL GENETICS, 2014, 51 (05) :283-293
[52]   Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts [J].
Vasen, Hans F. A. ;
Blanco, Ignacio ;
Aktan-Collan, Katja ;
Gopie, Jessica P. ;
Alonso, Angel ;
Aretz, Stefan ;
Bernstein, Inge ;
Bertario, Lucio ;
Burn, John ;
Capella, Gabriel ;
Colas, Chrystelle ;
Engel, Christoph ;
Frayling, Ian M. ;
Genuardi, Maurizio ;
Heinimann, Karl ;
Hes, Frederik J. ;
Hodgson, Shirley V. ;
Karagiannis, John A. ;
Lalloo, Fiona ;
Lindblom, Annika ;
Mecklin, Jukka-Pekka ;
Moller, Pal ;
Myrhoj, Torben ;
Nagengast, Fokko M. ;
Parc, Yann ;
de Leon, Maurizio Ponz ;
Renkonen-Sinisalo, Laura ;
Sampson, Julian R. ;
Stormorken, Astrid ;
Sijmons, Rolf H. ;
Tejpar, Sabine ;
Thomas, Huw J. W. ;
Rahner, Nils ;
Wijnen, Juul T. ;
Jaervinen, Heikki Juhani ;
Moeslein, Gabriela .
GUT, 2013, 62 (06) :812-823
[53]   Cancer Genome Landscapes [J].
Vogelstein, Bert ;
Papadopoulos, Nickolas ;
Velculescu, Victor E. ;
Zhou, Shibin ;
Diaz, Luis A., Jr. ;
Kinzler, Kenneth W. .
SCIENCE, 2013, 339 (6127) :1546-1558
[54]   Neurofibromatosis type 1 gene as a mutational target in a mismatch repair-deficient cell type [J].
Wang, Q ;
Montmain, G ;
Ruano, E ;
Upadhyaya, M ;
Dudley, S ;
Liskay, RM ;
Thibodeau, SN ;
Puisieux, A .
HUMAN GENETICS, 2003, 112 (02) :117-123
[55]   Homozygous PMS2 deletion causes a severe colorectal cancer and multiple adenorna phenotype without extraintestinal cancer [J].
Will, Olivia ;
Carvajal-Carmona, Luis G. ;
Gorman, Patricia ;
Howarth, Kimberley M. ;
Jones, Angela M. ;
Polanco-Echeverry, Guadalupe M. ;
Chinaleong, Jo-Anne ;
Gunther, Thomas ;
Silver, Andrew ;
Clark, Susan K. ;
Tomlinson, An .
GASTROENTEROLOGY, 2007, 132 (02) :527-530
[56]   Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg? [J].
Wimmer, Katharina ;
Etzler, Julia .
HUMAN GENETICS, 2008, 124 (02) :105-122
[57]   Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'Care for CMMRD' (C4CMMRD) [J].
Wimmer, Katharina ;
Kratz, Christian P. ;
Vasen, Hans F. A. ;
Caron, Olivier ;
Colas, Chrystelle ;
Entz-Werle, Natacha ;
Gerdes, Anne-Marie ;
Goldberg, Yael ;
Ilencikova, Denisa ;
Muleris, Martine ;
Duval, Alex ;
Lavoine, Noemie ;
Ruiz-Ponte, Clara ;
Slavc, Irene ;
Burkhardt, Brigit ;
Brugieres, Laurence .
JOURNAL OF MEDICAL GENETICS, 2014, 51 (06) :355-365
[58]   Constitutional mismatch repair-deficiency syndrome [J].
Wimmer, Katharina ;
Kratz, Christian P. .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2010, 95 (05) :699-701