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               <dc:title>Long-term efficacy of first-line ibrutinib treatment for chronic lymphocytic leukaemia in patients with TP53 aberrations : a pooled analysis from four clinical trials</dc:title>
               <dc:creator>Allan, John N.</dc:creator>
               <dc:creator>Shanafelt, Tait</dc:creator>
               <dc:creator>Wiestner, Adrian</dc:creator>
               <dc:creator>Moreno, Carol</dc:creator>
               <dc:creator>O'Brien, Susan M.</dc:creator>
               <dc:creator>Li, Jianling</dc:creator>
               <dc:creator>Krigsfeld, Gabriel</dc:creator>
               <dc:creator>Dean, James P.</dc:creator>
               <dc:creator>Ahn, Inhye E.</dc:creator>
               <dc:creator>Universitat Autònoma de Barcelona</dc:creator>
               <dc:subject>Chronic lymphocytic leukaemia</dc:subject>
               <dc:subject>Del(17p)</dc:subject>
               <dc:subject>First-line</dc:subject>
               <dc:subject>Ibrutinib</dc:subject>
               <dc:subject>TP53 mutation</dc:subject>
               <dc:description>TP53 aberrations [del(17p) or TP53 mutation] predict poor survival with chemoimmunotherapy in patients with chronic lymphocytic leukaemia (CLL). We evaluated long-term efficacy and safety of first-line ibrutinib-based therapy in patients with CLL bearing TP53 aberrations in a pooled analysis across four studies: PCYC-1122e, RESONATE-2 (PCYC-1115/16), iLLUMINATE (PCYC-1130) and ECOG-ACRIN E1912. The pooled analysis included 89 patients with TP53 aberrations receiving first-line treatment with single-agent ibrutinib (n = 45) or ibrutinib in combination with an anti-CD20 antibody (n = 44). All 89 patients had del(17p) (53% of 89 patients) and/or TP53 mutation (91% of 58 patients with TP53 sequencing results available). With a median follow-up of 49·8 months (range, 0·1-95·9), median progression-free survival was not reached. Progression-free survival rate and overall survival rate estimates at four years were 79% and 88%, respectively. Overall response rate was 93%, including complete response in 39% of patients. No new safety signals were identified in this analysis. Forty-six percent of patients remained on ibrutinib treatment at last follow-up. With median follow-up of four years (up to eight years), results from this large, pooled, multi-study data set suggest promising long-term outcomes of first-line ibrutinib-based therapy in patients with TP53 aberrations. Registered at ClinicalTrials.gov (NCT01500733, NCT01722487, NCT02264574 and NCT02048813).</dc:description>
               <dc:date>2024-11-04T06:25:35Z</dc:date>
               <dc:date>2024-11-04T06:25:35Z</dc:date>
               <dc:date>2021</dc:date>
               <dc:type>Article</dc:type>
               <dc:identifier>http://hdl.handle.net/2072/470447</dc:identifier>
               <dc:relation>British Journal of Haematology ; Vol. 196 (december 2021), p. 947-953</dc:relation>
               <dc:rights>open access</dc:rights>
               <dc:rights>Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades.</dc:rights>
               <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
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