scholarly journals Postibrutinib outcomes in patients with mantle cell lymphoma

Blood ◽  
2016 ◽  
Vol 127 (12) ◽  
pp. 1559-1563 ◽  
Author(s):  
Peter Martin ◽  
Kami Maddocks ◽  
John P. Leonard ◽  
Jia Ruan ◽  
Andre Goy ◽  
...  

Key Points Patients with mantle cell lymphoma who progressed during treatment with ibrutinib have a poor outcome. There are no therapies that appear to be uniquely successful in the postibrutinib setting. The postibrutinib setting is an unmet need.

Blood ◽  
2015 ◽  
Vol 125 (17) ◽  
pp. 2669-2677 ◽  
Author(s):  
Simon Husby ◽  
Ulrik Ralfkiaer ◽  
Christian Garde ◽  
Roza Zandi ◽  
Sara Ek ◽  
...  

Key Points miR-18b overexpression identified patients with poor prognosis in 2 large prospective homogenously treated MCL cohorts. miR-18b overexpression adds prognostic information to the MIPI-B prognosticator.


Blood ◽  
2014 ◽  
Vol 123 (11) ◽  
pp. 1665-1673 ◽  
Author(s):  
Julie E. Chang ◽  
Hailun Li ◽  
Mitchell R. Smith ◽  
Randy D. Gascoyne ◽  
Elisabeth M. Paietta ◽  
...  

Key Points VcR-CVAD produced high overall and CR rates in previously untreated MCL patients. No substantial difference in 3-year PFS or OS was observed in patients receiving ASCT compared with patients receiving maintenance rituximab.


Blood ◽  
2015 ◽  
Vol 126 (5) ◽  
pp. 604-611 ◽  
Author(s):  
Marie-Hélène Delfau-Larue ◽  
Wolfram Klapper ◽  
Françoise Berger ◽  
Fabrice Jardin ◽  
Josette Briere ◽  
...  

Key Points CDKN2A and TP53 deletions remain of bad prognostic value in younger MCL patients treated according to the current standard of care. CDKN2A and TP53 deletions have independent deleterious effects and should be considered for treatment decisions in addition to MIPI and Ki-67 index.


Blood ◽  
2017 ◽  
Vol 130 (17) ◽  
pp. 1903-1910 ◽  
Author(s):  
Christian W. Eskelund ◽  
Christina Dahl ◽  
Jakob W. Hansen ◽  
Maj Westman ◽  
Arne Kolstad ◽  
...  

Key Points The intensified standard-of-care regimens for younger patients with MCL do not overcome the deleterious effects of TP53 mutations. MCLs with TP53 mutations should be considered for alternative frontline treatment.


2019 ◽  
Vol 3 (20) ◽  
pp. 3132-3135 ◽  
Author(s):  
Manali Kamdar ◽  
Hongli Li ◽  
Robert W. Chen ◽  
Lisa M. Rimsza ◽  
Michael L. Leblanc ◽  
...  

Key Points Five-year follow-up of S1106 demonstrates similar efficacy, MRD negativity, and 5-year survival with RH or RB, but RH was more toxic than RB. RB showed excellent efficacy and survival and less toxicity compared with a cytarabine-based regimen in transplant-eligible MCL patients.


Blood ◽  
2016 ◽  
Vol 128 (21) ◽  
pp. 2517-2526 ◽  
Author(s):  
Caron Jacobson ◽  
Nadja Kopp ◽  
Jacob V. Layer ◽  
Robert A. Redd ◽  
Sebastian Tschuri ◽  
...  

Key Points Inhibition of HSP90 targets multiple dependences in mantle cell lymphoma. Clinically available HSP90 inhibitors overcome ibrutinib resistance in vitro and in vivo.


Blood ◽  
2017 ◽  
Vol 130 (6) ◽  
pp. 763-776 ◽  
Author(s):  
Han Zhang ◽  
Zheng Chen ◽  
Roberto N. Miranda ◽  
L. Jeffrey Medeiros ◽  
Nami McCarty

Key Points Downregulation of BACH2 increases MCL proliferation, dispersal, and drug resistance. Distinct crosstalk between BACH2 and HIF-1α under different physiological conditions modifies MCL properties.


Blood ◽  
2015 ◽  
Vol 126 (13) ◽  
pp. 1565-1574 ◽  
Author(s):  
Baohua Sun ◽  
Bhavin Shah ◽  
Warren Fiskus ◽  
Jun Qi ◽  
Kimal Rajapakshe ◽  
...  

Key Points BA reduces MYC, CDK4/6, nuclear RelA, and BTK expression and is synergistically lethal with ibrutinib in MCL cells. Cotreatment with BA and inhibitor of BCL2, CDK4/6, or histone deacetylases is synergistically lethal against ibrutinib-resistant MCL cells.


Blood ◽  
2014 ◽  
Vol 124 (14) ◽  
pp. 2235-2247 ◽  
Author(s):  
Jara Palomero ◽  
Maria Carmela Vegliante ◽  
Marta Leonor Rodríguez ◽  
Álvaro Eguileor ◽  
Giancarlo Castellano ◽  
...  

Key Points SOX11 mediates regulation of angiogenesis via the PDGFA signaling pathway in MCL. SOX11-dependent increased angiogenesis contributes to a more aggressive MCL phenotype.


Blood ◽  
2014 ◽  
Vol 123 (6) ◽  
pp. 884-893 ◽  
Author(s):  
Samuel G. Katz ◽  
James L. LaBelle ◽  
Hailong Meng ◽  
Regina P. Valeriano ◽  
Jill K. Fisher ◽  
...  

Key Points Immune stimulation of cyclin D1 transgenic mice bearing Bim-deficient B cells induces an MCL phenotype. The induced lymphoma of EμCycD1CD19CREBimfl/fl mice highlights the collaborative roles of Bim deletion and cyclin D1 expression in MCL.


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