Literature DB >> 21564078

Attainment of complete/very good partial response following rituximab-based therapy is an important determinant to progression-free survival, and is impacted by polymorphisms in FCGR3A in Waldenstrom macroglobulinaemia.

Steven P Treon1, Guang Yang, Christine Hanzis, Leukothea Ioakimidis, Sigitas J Verselis, Edward A Fox, Lian Xu, Zachary R Hunter, Hsiuyi Tseng, Robert J Manning, Christopher J Patterson, Patricia Sheehy, Barry Turnbull.   

Abstract

The incorporation of rituximab into various regimens has improved depth of response in Waldenstrom macroglobulinaemia (WM), though the impact of achieving better responses remains to be determined. We examined response depth on progression-free survival (PFS) in 159 rituximab-naïve WM patients who received rituximab-based therapy. The median follow-up was 33·5 months, and categorical responses were as follows: complete response (CR, 8·8%); very good partial response (VGPR, 13·2%); partial response (50%); minor response (18·9%); Non-Responders (8·8%). Sequencing for polymorphic variants of FCGR2A, FCGR2B, and FCGR3A was performed, and impact on response depth determined. Achievement of better categorical responses was incrementally associated with improved PFS (P < 0·0001). No separation was observed between CR and VGPR, and attainment of at least a VGPR was associated with improved time-to-progression. Neither age, serum IgM, haematocrit, platelet count, serum β(2) microglobulin, WM International Prognostic Scoring System score, and treatment group predicted for CR/VGPR. Polymorphisms at FCGR3A-48 and -158 were associated with improved categorical responses, particularly attainment of CR/VGPR (P ≤ 0·03). The attainment of CR/VGPR was associated with significantly longer PFS in rituximab-naïve WM patients undergoing rituximab-based therapy, and was predicted by polymorphisms in FCGR3A.
© 2011 Blackwell Publishing Ltd.

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Year:  2011        PMID: 21564078     DOI: 10.1111/j.1365-2141.2011.08726.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  16 in total

1.  Onsets of progression and second treatment determine survival of patients with symptomatic Waldenström macroglobulinemia.

Authors:  Stephanie Guidez; Julien Labreuche; Elodie Drumez; Loic Ysebaert; Jana Bakala; Caroline Delette; Bénédicte Hivert; Caroline Protin; Hervé Declercq; Mélanie Verlay; Jean Pierre Marolleau; Alain Duhamel; Pierre Morel
Journal:  Blood Adv       Date:  2018-11-27

2.  Carfilzomib: a new opportunity for WM patients.

Authors:  Enrica Morra
Journal:  Blood       Date:  2014-07-24       Impact factor: 22.113

3.  Disease control should be the goal of therapy for WM patients.

Authors:  Efstathios Kastritis; Meletios A Dimopoulos
Journal:  Blood Adv       Date:  2017-11-28

4.  What should be the goal of therapy for Waldenström macroglobulinemia patients? Complete response should be the goal of therapy.

Authors:  Steven P Treon; Jorge J Castillo
Journal:  Blood Adv       Date:  2017-11-28

Review 5.  Genetic factors and pathogenesis of Waldenström's macroglobulinemia.

Authors:  Jorge Monge; Esteban Braggio; Stephen M Ansell
Journal:  Curr Oncol Rep       Date:  2013-10       Impact factor: 5.075

6.  A randomized phase 3 trial of zanubrutinib vs ibrutinib in symptomatic Waldenström macroglobulinemia: the ASPEN study.

Authors:  Constantine S Tam; Stephen Opat; Shirley D'Sa; Wojciech Jurczak; Hui-Peng Lee; Gavin Cull; Roger G Owen; Paula Marlton; Björn E Wahlin; Ramón Garcia Sanz; Helen McCarthy; Stephen Mulligan; Alessandra Tedeschi; Jorge J Castillo; Jaroslaw Czyz; Carlos Fernández de Larrea; David Belada; Edward Libby; Jeffrey V Matous; Marina Motta; Tanya Siddiqi; Monica Tani; Marek Trneny; Monique C Minnema; Christian Buske; Veronique Leblond; Judith Trotman; Wai Y Chan; Jingjing Schneider; Sunhee Ro; Aileen Cohen; Jane Huang; Meletios Dimopoulos
Journal:  Blood       Date:  2020-10-29       Impact factor: 22.113

7.  MYD88 L265P in Waldenström macroglobulinemia, immunoglobulin M monoclonal gammopathy, and other B-cell lymphoproliferative disorders using conventional and quantitative allele-specific polymerase chain reaction.

Authors:  Lian Xu; Zachary R Hunter; Guang Yang; Yangsheng Zhou; Yang Cao; Xia Liu; Enrica Morra; Alessandra Trojani; Antonino Greco; Luca Arcaini; Marzia Varettoni; Maria Varettoni; Jennifer R Brown; Yu-Tzu Tai; Kenneth C Anderson; Nikhil C Munshi; Christopher J Patterson; Robert J Manning; Christina K Tripsas; Neal I Lindeman; Steven P Treon
Journal:  Blood       Date:  2013-01-15       Impact factor: 22.113

8.  Zanubrutinib for the treatment of patients with Waldenström macroglobulinemia: 3 years of follow-up.

Authors:  Judith Trotman; Stephen Opat; David Gottlieb; David Simpson; Paula Marlton; Gavin Cull; Javier Munoz; Alessandra Tedeschi; Andrew W Roberts; John F Seymour; Siminder Kaur Atwal; Yiling Yu; William Novotny; Eric Holmgren; Ziwen Tan; James D Hilger; Jane Huang; Constantine S Tam
Journal:  Blood       Date:  2020-10-29       Impact factor: 22.113

9.  Zanubrutinib for the treatment of MYD88 wild-type Waldenström macroglobulinemia: a substudy of the phase 3 ASPEN trial.

Authors:  Meletios Dimopoulos; Ramon Garcia Sanz; Hui-Peng Lee; Marek Trneny; Marzia Varettoni; Stephen Opat; Shirley D'Sa; Roger G Owen; Gavin Cull; Stephen Mulligan; Jaroslaw Czyz; Jorge J Castillo; Marina Motta; Tanya Siddiqi; Mercedes Gironella Mesa; Miquel Granell Gorrochategui; Dipti Talaulikar; Pier Luigi Zinzani; Elham Askari; Sebastian Grosicki; Albert Oriol; Simon Rule; Janusz Kloczko; Alessandra Tedeschi; Christian Buske; Veronique Leblond; Judith Trotman; Wai Y Chan; Jan Michel; Jingjing Schneider; Ziwen Tan; Aileen Cohen; Jane Huang; Constantine S Tam
Journal:  Blood Adv       Date:  2020-12-08

10.  Partial response or better at six months is prognostic of superior progression-free survival in Waldenström macroglobulinaemia patients treated with ibrutinib.

Authors:  Jorge J Castillo; Jithma P Abeykoon; Joshua N Gustine; Saurabh Zanwar; Kirsten Mein; Catherine A Flynn; Maria G Demos; Maria L Guerrera; Amanda Kofides; Xia Liu; Manit Munshi; Nickolas Tsakmaklis; Rebecca King; Guang Yang; Zachary R Hunter; Ranjana H Advani; Maria Lia Palomba; Stephen M Ansell; Morie A Gertz; Prashant Kapoor; Steven P Treon
Journal:  Br J Haematol       Date:  2020-11-18       Impact factor: 6.998

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