Ghulam J. Mufti
University of Cambridge
691 Papers
5.2K Citations
Ghulam J. Mufti is an academic researcher from University of Cambridge. The author has contributed to research in topics: Transplantation & Myelodysplastic syndromes. The author has an hindex of 88, co-authored 687 publications. Previous affiliations of Ghulam J. Mufti include Anthony Nolan & Stanford University.
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Papers
Myelodysplastic syndromes: a scoring system with prognostic significance
TL;DR: 141 patients with MDS were classified according to the FAB criteria and followed up for a period of 4–192 months, separating patients with RA, RAS, RAEB into good and bad prognostic groups.
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A randomized phase 3 study of lenalidomide versus placebo in RBC transfusion-dependent patients with Low-/Intermediate-1-risk myelodysplastic syndromes with del5q
Pierre Fenaux,Aristoteles Giagounidis,Dominik Selleslag,Odile Beyne-Rauzy,Ghulam J. Mufti,Moshe Mittelman,Petra Muus,Peter A. W. te Boekhorst,Guillermo Sanz,Consuelo del Cañizo,Agnes Guerci-Bresler,Lennart Nilsson,Uwe Platzbecker,Michael Lübbert,Bruno Quesnel,Mario Cazzola,Arnold Ganser,David G. Bowen,Brigitte Schlegelberger,Carlo Aul,Robert Knight,John Francis,Tommy Fu,Eva Hellström-Lindberg +23 more
TL;DR: Lenalidomide is beneficial and has an acceptable safety profile in transfusion-dependent patients with Low-/Intermediate-1-risk del5q myelodysplastic syndrome and the safety profile was consistent with previous reports.
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TP53 Mutations in Low-Risk Myelodysplastic Syndromes With del(5q) Predict Disease Progression
Martin Jädersten,Leonie Saft,Alexander E. Smith,Austin G. Kulasekararaj,Sabine Pomplun,Gudrun Göhring,Anette Hedlund,Robert Hast,Brigitte Schlegelberger,Anna Porwit,Eva Hellström-Lindberg,Ghulam J. Mufti +11 more
TL;DR: It is demonstrated that TP53 mutated populations may occur at an early disease stage in almost a fifth of low-risk MDS patients with del(5q) and could indicate a previously unrecognized heterogeneity of the disease which may significantly affect clinical decision making.
474
Luspatercept in Patients with Lower-Risk Myelodysplastic Syndromes
Pierre Fenaux,Pierre Fenaux,Uwe Platzbecker,Ghulam J. Mufti,Guillermo Garcia-Manero,Rena Buckstein,Valeria Santini,María Díez-Campelo,Carlo Finelli,Mario Cazzola,Osman Ilhan,Mikkael A. Sekeres,Jose F Falantes,Beatriz Arrizabalaga,Flavia Salvi,Valentina Giai,Paresh Vyas,David T. Bowen,Dominik Selleslag,Amy E. DeZern,Joseph G. Jurcic,Ulrich Germing,Katharina Goetze,Bruno Quesnel,Odile Beyne-Rauzy,Thomas Cluzeau,Maria-Teresa Voso,Dominiek Mazure,Edo Vellenga,Peter L. Greenberg,Eva Hellström-Lindberg,Amer M. Zeidan,Lionel Ades,Lionel Ades,Amit Verma,Michael R. Savona,Abderrahmane Laadem,Aziz Benzohra,Jennie Zhang,Anita Rampersad,Diana Ronai Dunshee,Peter G. Linde,Matthew L. Sherman,Rami S. Komrokji,Alan F. List +44 more
TL;DR: Luspatercept reduced the severity of anemia in patients with lower-risk myelodysplastic syndromes with ring sideroblasts who had been receiving regular red-cell transfusions and who had disease that was refractory to or unlikely to respond to erythropoiesis-stimulating agents or who had discontinued such agents owing to an adverse event.
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The role of apoptosis, proliferation, and the Bcl-2–related proteins in the myelodysplastic syndromes and acute myeloid leukemia secondary to MDS
Jane Parker,Ghulam J. Mufti,Feyrooz Rasool,Aleksandar Mijovic,Stephen Devereux,Antonio Pagliuca +5 more
TL;DR: It is indicated that MDS progression arises through multiple hits that alter levels of CD34(+) cell apoptosis and proliferation and is inversely correlated with both International Prognostic Scoring System score and cytogenetic risk group; highest levels observed in patients with low score and/or good risk cytogenetics.
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