Literature DB >> 26890983

Calreticulin variant stratified driver mutational status and prognosis in essential thrombocythemia.

Yoseph C Elala1,2, Terra L Lasho1,2, Naseema Gangat1,2, Christy Finke1,2, Daniela Barraco1,2, Mahnur Haider1,2, Ahmed K Abou Hussein1,2, Curtis A Hanson3,4, Rhett P Ketterling4,5, Animesh Pardanani1,2, Ayalew Tefferi1,2.   

Abstract

About 85% of patients with essential thrombocythemia (ET) harbor one of three driver mutations: JAK2, calreticulin (CALR), and MPL; the remaining ( ∼15%) are wild type for all three mutations and are referred to as being "triple negative." Furthermore, CALR mutations in ET are structurally classified as type 1/type 1-like or type 2/type 2-like variants. The objective of the current study was to examine the impact of CALR mutation variant stratified driver mutational status on overall (OS), myelofibrosis-free (MFFS), thrombosis-free, and leukemia-free survival (LFS) in ET; 495 patients (median age 58 years; 61% females) with ET were fully annotated for the their driver mutational status: 321 (65%) harbored JAK2, 109 (22%) CALR, and 12 (2%) MPL mutations and 11% were triple-negative. Among the 109 CALR-mutated cases, 52% were classified as type 1/type 1-like and 48% as type 2/type 2-like. In univariate analysis, triple-negative patients displayed the best and MPL mutated the worst OS (P = 0.007); however, the difference in OS was no longer apparent on multivariable analysis that included age and sex as covariates (P = 0.5). LFS was also similar among the different mutational groups (P = 0.6) whereas MFFS was significantly shorter in MPL-mutated patients on both univariate and multivariable analyses (age-adjusted P = 0.02; HR 7.9, 95% CI 2.0-31.5). Also in multivariable analysis that included thrombosis history, age, and cardiovascular risk factors, the presence of JAK2 or MPL mutations was independently associated with higher risk of thrombosis (P = 0.02; HR 1.9, 95% CI 1.1-3.4). In conclusion, driver mutational status in ET does not appear to influence overall or LFS, even after CALR variant stratification. However, the presence of MPL mutations might be associated with a higher risk of fibrotic transformation and the presence of JAK2/MPL mutations with higher risk of thrombosis.
© 2016 Wiley Periodicals, Inc.

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Year:  2016        PMID: 26890983     DOI: 10.1002/ajh.24338

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  19 in total

1.  2016 WHO Clinical Molecular and Pathological Criteria for Classification and Staging of Myeloproliferative Neoplasms (MPN) Caused by MPN Driver Mutations in the JAK2, MPL and CALR Genes in the Context of New 2016 WHO Classification: Prognostic and Therapeutic Implications.

Authors:  Jan Jacques Michiels; Mihaela Tevet; Adrian Trifa; Emilia Niculescu-Mizil; Anca Lupu; Ana Maria Vladareanu; Horia Bumbea; Anca Ilea; Camelia Dobrea; Daniela Georgescu; Oana Patrinoiu; Mihaela Popescu; Meilin Murat; Cornel Dragan; Felicia Mihai; Sabina Zurac; Silvana Angelescu; Anamaria Iova; Alina Popa; Rodica Gogulescu; Violeta Popov
Journal:  Maedica (Bucur)       Date:  2016-03

Review 2.  Mutations in MPNs: prognostic implications, window to biology, and impact on treatment decisions.

Authors:  Jamile M Shammo; Brady L Stein
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

3.  Driver mutations' effect in secondary myelofibrosis: an international multicenter study based on 781 patients.

Authors:  F Passamonti; B Mora; T Giorgino; P Guglielmelli; M Cazzola; M Maffioli; A Rambaldi; M Caramella; R Komrokji; J Gotlib; J J Kiladjian; F Cervantes; T Devos; F Palandri; V De Stefano; M Ruggeri; R Silver; G Benevolo; F Albano; D Caramazza; E Rumi; M Merli; D Pietra; R Casalone; T Barbui; L Pieri; A M Vannucchi
Journal:  Leukemia       Date:  2016-11-25       Impact factor: 11.528

4.  Mutant calreticulin in myeloproliferative neoplasms.

Authors:  Joan How; Gabriela S Hobbs; Ann Mullally
Journal:  Blood       Date:  2019-12-19       Impact factor: 22.113

Review 5.  SOHO State-of-the-Art Update and Next Questions: MPN.

Authors:  Prithviraj Bose; Jason Gotlib; Claire N Harrison; Srdan Verstovsek
Journal:  Clin Lymphoma Myeloma Leuk       Date:  2018-01

6.  JAK2, CALR, MPL and ASXL1 mutational status correlates with distinct histological features in Philadelphia chromosome-negative myeloproliferative neoplasms.

Authors:  Waihay J Wong; Robert P Hasserjian; Geraldine S Pinkus; Lawrence J Breyfogle; Ann Mullally; Olga Pozdnyakova
Journal:  Haematologica       Date:  2017-11-16       Impact factor: 9.941

7.  Rare type 1-like and type 2-like calreticulin mutants induce similar myeloproliferative neoplasms as prevalent type 1 and 2 mutants in mice.

Authors:  Katte Rao Toppaldoddi; Maira da Costa Cacemiro; Olivier Bluteau; Barbara Panneau-Schmaltz; Amélie Pioch; Delphine Muller; Jean-Luc Villeval; Hana Raslova; Stefan N Constantinescu; Isabelle Plo; William Vainchenker; Caroline Marty
Journal:  Oncogene       Date:  2018-10-19       Impact factor: 9.867

8.  Acute splenic infarction presenting as an unusual manifestation of essential thrombocythaemia with normal platelet count.

Authors:  Katsuyuki Yoshida; Ibuki Kurihara; Takahiko Fukuchi; Hitoshi Sugawara
Journal:  BMJ Case Rep       Date:  2019-07-03

Review 9.  Post-ET and Post-PV Myelofibrosis: Updates on a Distinct Prognosis from Primary Myelofibrosis.

Authors:  Francesco Passamonti; Barbara Mora; Daniela Barraco; Margherita Maffioli
Journal:  Curr Hematol Malig Rep       Date:  2018-06       Impact factor: 3.952

10.  Calreticulin-mutant proteins induce megakaryocytic signaling to transform hematopoietic cells and undergo accelerated degradation and Golgi-mediated secretion.

Authors:  Lijuan Han; Claudia Schubert; Johanna Köhler; Mirle Schemionek; Susanne Isfort; Tim H Brümmendorf; Steffen Koschmieder; Nicolas Chatain
Journal:  J Hematol Oncol       Date:  2016-05-13       Impact factor: 17.388

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