MYD88 mutation status does not impact overall survival in Waldenstrom macroglobulinemia

被引：63

作者：

Abeykoon, Jithma P. ^{[1
]}

Paludo, Jonas ^{[1
,2
]}

King, Rebecca L. ^{[3
]}

Ansell, Stephen M. ^{[1
,2
]}

Gertz, Morie A. ^{[1
,2
]}

LaPlant, Betsy R. ^{[4
]}

Halvorson, Alese E. ^{[4
]}

Gonsalves, Wilson I. ^{[1
,2
]}

Dingli, David ^{[1
,2
]}

Fang, Hong ^{[3
]}

Rajkumar, S. Vincent ^{[1
,2
]}

Lacy, Martha Q. ^{[1
,2
]}

He, Rong ^{[3
]}

Kourelis, Taxiarchis ^{[1
]}

Reeder, Craig B. ^{[5
]}

Novak, Anne J. ^{[2
]}

McPhail, Ellen D. ^{[3
]}

Viswanatha, David S. ^{[3
]}

Witzig, Thomas E. ^{[1
,2
]}

Go, Ronald S. ^{[1
,2
]}

Habermann, Thomas M. ^{[1
,2
]}

Buadi, Francis K. ^{[1
,2
]}

Dispenzieri, Angela ^{[1
,2
]}

Leung, Nelson ^{[1
,2
]}

Lin, Yi ^{[1
,2
]}

Thompson, Carrie A. ^{[1
,2
]}

Hayman, Suzanne R. ^{[1
,2
]}

Kyle, Robert A. ^{[1
,2
]}

Kumar, Shaji K. ^{[1
,2
]}

Kapoor, Prashant ^{[1
,2
]}

机构：

[1] Mayo Clin, Dept Internal Med, Rochester, MN USA

[2] Mayo Clin, Div Hematol, Rochester, MN USA

[3] Mayo Clin, Div Hematopathol, Rochester, MN USA

[4] Mayo Clin, Div Biomed Stat, Rochester, MN USA

[5] Mayo Clin, Div Hematol, Scottsdale, AZ USA

来源：

AMERICAN JOURNAL OF HEMATOLOGY | 2018年 / 93卷 / 02期

关键词：

L265P SOMATIC MUTATION; IGM MONOCLONAL GAMMOPATHY; B-CELL LYMPHOMA; THERAPY; CXCR4; PROGRESSION; RITUXIMAB; CYCLOPHOSPHAMIDE; TRANSFORMATION; RESISTANCE;

D O I：

10.1002/ajh.24955

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Waldenstrom macroglobulinemia (WM) is an immunoglobulin M-associated lymphoma, with majority of cases demonstrating MYD88 locus alteration, most commonly, MYD88(L265P). Owing to low prevalence of the wild-type (WT) MYD88 genotype in WM, clinically relevant data in this patient population are sparse, with one study showing nearly a 10-fold increased risk of mortality in this subgroup compared to patients with MYD88(L265P) mutation. We studied a large cohort of patients with MYD88(L265P) and MYD88(WT) WM, evaluated at Mayo Clinic, Rochester, between 1995 and 2016, to specifically assess the impact of these genotypes on clinical course. Of 557 patients, MYD88(L265P) mutation status, as determined by allele-specific polymerase chain reaction, was known in 219, and 174 (79%) of those exhibited MYD88(L265P), 157 of 174 patients had active disease. Of 45 (21%) patients with MYD88(WT) genotype, 44 had active disease. The estimated median follow-up was 7.0 years; median overall survival was 10.2 years (95% CI: 8.4-16.5) for MYD88(L265P) versus 13.9 years (95% CI: 6.4-29.3) for the MYD88(WT) (P = 0.86). The time-to-next therapy from frontline treatment and the presenting features were similar in the two patient populations. For patients with smoldering WM at diagnosis, the median time-to-progression to active disease was 2.8 years (95% CI: 2.2-3.8) in the MYD88(L265P) cohort and 1.9 years (95% CI: 0.7-3.1) in the MYD88(WT) cohort (P = 0.21). The frequency of transformation to high-grade lymphoma, or the development of therapy-elated myelodysplastic syndrome was higher in the MYD88(WT) cohort (16% versus 4% in the MYD88(L265P), P = 0.009). In conclusion, MYD88(L265P) mutation does not appear to be a determinant of outcome, and its presence may not be a disease-defining feature in WM. Our findings warrant external validation, preferably through prospective studies.

引用

页码：187 / 194

页数：8

共 45 条

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