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    Advances in Hematology

    Subject:
    Hematology
    Publisher:
    Hindawi — Wiley
    ISSN:
    1687-9104
    Scimago Journal Rank:
    34

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    journal article
    LitStream Collection
    Utility of Bruton’s Tyrosine Kinase Inhibitors in Light Chain Amyloidosis Caused by Lymphoplasmacytic Lymphoma (Waldenström’s Macroglobulinemia)

    Bou Zerdan, Maroun;Valent, Jason;Diacovo, Maria Julia;Theil, Karl;Chaulagain, Chakra P.

    2022 Advances in Hematology

    doi: 10.1155/2022/1182384pmid: 35096069

    Of the variety of immunoglobulin related amyloidosis (AL), immunoglobulin M (IgM) related AL represents only 6 to 10&#x0025; of affected patients, and the majority of these cases are associated with underlying non-Hodgkin&#x2019;s Lymphoma including Waldenstr&#xf6;m&#x2019;s macroglobulinemia (WM). Ibrutinib, acalabrutinib, and zanubrutinib are Bruton tyrosine kinase (BTK) inhibitors approved for certain indolent B cell non-Hodgkin&#x2019;s lymphoma (NHL). BTK is a nonreceptor kinase involved in B-cell survival, proliferation, and interaction with the microenvironment. We retrospectively evaluated the tolerability and effectiveness of BTK inhibitors ibrutinib and acalabrutinib therapy in (<i>n</i>&#x2009;&#x3d;&#x2009;4) patients with IgM-related AL amyloidosis with underlying WM. Treatment was well tolerated with both hematologic and organ response in patients with AL amyloidosis in the setting of WM. Atrial fibrillation led to the discontinuation of ibrutinib in one patient, and acalabrutinib caused significant thumb hematoma needing dose reduction in another patient. All patients evaluated had the MYD88 mutation. This may explain the good response to BTK inhibitors therapy in our series. BTK inhibitors should be further investigated in larger prospective studies for treatment of AL amyloidosis in patients with lymphoplasmacytic lymphoma/WM.
    journal article
    Open Access Collection
    Ibrutinib plus Obinutuzumab as Frontline Therapy for Chronic Lymphocytic Leukemia Is Associated with a Lower Rate of Infusion-Related Reactions and with Sustained Remissions after Ibrutinib Discontinuation: A Single-Arm, Open-Label, Phase 1b/2 Clinical Trial NCT0231576

    Castro, Januario E.;Lengerke-Diaz, Paula A.;Velez Lujan, Juliana;Choi, Michael Y.;Moreno-Cortes, Eider F.;Forero, Jose V.;Garcia-Robledo, Juan Esteban;Jacobs, Chaja;McCarthy, Colin;Heinen, Alaina;Amaya-Chanaga, Carlos I.;Kipps, Thomas J.

    2022 Advances in Hematology

    doi: 10.1155/2022/4450824pmid: 35103064

    journal article
    LitStream Collection
    Anaemia Prevalence More Than Doubles in an Academic Year in a Cohort of Tertiary Students: A Repeated-Measure Study in Cape Coast, Ghana

    Amoaning, Regina Elorm;Amoako, Ernestina Siaw;Kyiire, Grace Arezie;Owusu, Dennis Dela;Bruce, Happy;Simpong, David Larbi;Adu, Patrick

    2022 Advances in Hematology

    doi: 10.1155/2022/4005208pmid: 35103063

    <i>Background</i>. The stress of academic life may predispose young adults to poor dietary habits, which could potentially precipitate nutritional deficiencies, such as iron deficiency. This study evaluated factors predictive of optimal iron stores as well as changes in haematological parameters over the course of an academic year in a cohort of tertiary students. <i>Materials and Methods</i>. The repeated-measure cohort study recruited 117 undergraduate students from September 2018 to May 2019. Venous blood samples were drawn for full blood count estimation, qualitative glucose-6-phosphate dehydrogenase (G6PD) status, haemoglobin variants, and blood group determination during the first 2 weeks of semester 1. However, anthropometric parameters as well as full blood counts were determined for each participant during the first week and last week of semesters 1 and 2. Additionally, semistructured questionnaires were used to capture sociodemographic data. Also, serum ferritin was estimated for each participant using enzyme-linked immunosorbent assay. <i>Results</i>. Overall, 23.1% and 15.5% of participants inherited G6PD defect (G6PDd) or haemoglobin variants, respectively. However, group O (68/117; 58.1%) was the predominant ABO blood group and an overwhelming 90.6% (106/117) inherited Rh D antigen. The prevalence of anaemia increased from 20% at the beginning of the first semester to 45.1% at the latter part of the second semester. G6PDd participants had significantly higher median serum ferritin than G6PD normal participants (<svg xmlns:xlink="http://www.w3.org/1999/xlink" xmlns="http://www.w3.org/2000/svg" style="vertical-align:-3.42943pt" id="M1" height="10.2124pt" version="1.1" viewBox="-0.0498162 -6.78297 7.83752 10.2124" width="7.83752pt"><g transform="matrix(.013,0,0,-0.013,0,0)"><path id="g113-113" d="M570 304C570 398 525 448 414 448C385 448 343 445 312 434L329 511L321 518C297 504 262 482 244 460L233 411C195 397 159 381 128 358L135 332C160 347 189 360 224 373L111 -147C97 -210 84 -218 17 -231L13 -257L254 -247L259 -218L233 -216C183 -212 177 -202 189 -142L218 -1C238 -10 266 -12 283 -12C351 3 429 48 483 105C543 168 570 242 570 304ZM482 289C482 161 380 33 304 33C278 33 248 51 233 69L303 396C326 400 352 403 369 403C428 403 482 380 482 289Z"/></g></svg> = 0.003). Also, a significantly higher proportion of females were iron depleted (25% vs. 2.3%) or iron deficient (14.3% vs. 9.3%) compared to males. Moreover, being male, G6PD deficient, or 21–25 years was associated with increased odds of participants having optimal serum ferritin levels. <i>Conclusion</i>. The progression of anaemia prevalence from mild to severe public health problem over the course of one academic year should urgently be addressed.
    journal article
    LitStream Collection
    Safety and Efficacy of Subcutaneous Rituximab in Previously Untreated Patients with CD20+ Diffuse Large B-Cell Lymphoma or Follicular Lymphoma: Results from an Italian Phase IIIb Study

    Petrini, Mario;Gaidano, Gianluca;Mengarelli, Andrea;Consoli, Ugo;Santoro, Armando;Liberati, Anna Maria;Ladetto, Marco;Fraticelli, Vincenzo;Guarini, Attilio;Mannina, Donato;Ferrando, Paola;Corradini, Paolo;Musto, Pellegrino;Stelitano, Caterina;Marino, Dario;Camera, Andrea;Murineddu, Marco;Battistini, Roberta;Caparrotti, Giuseppe;

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    Ibrutinib-based therapies are costly and require continuous administration. We hypothesized combining BTK inhibition with anti-CD20 monoclonal antibodies would yield deep remissions allowing discontinuation. We enrolled 32 therapy-na&#xef;ve CLL patients to receive ibrutinib plus obinutuzumab, followed by single-agent ibrutinib. Patients could discontinue ibrutinib after 36 months with sustained complete response (CR). We evaluated treatment safety, efficacy, and outcomes after ibrutinib discontinuation. The overall response rate was 100&#x0025;, 28&#x0025; achieved a CR, and 12.5&#x0025; achieved bone marrow undetectable minimal residual disease. At a three-year median follow-up, 91&#x0025; remain in remission with 100&#x0025; overall survival. Five patients in sustained CR stopped ibrutinib and have not progressed. Eight non-CR patients discontinued for other reasons, with only two progressing. The treatment was safe, with a lower IRR rate. All patients responded to treatment with longer time-to-progression after discontinuation of ibrutinib. Our data support the evaluation of ibrutinib discontinuation strategies in more extensive clinical trials (<a target="_blank" href="https://Clinicaltrials.gov">https://Clinicaltrials.gov</a> Identifier <a target="_blank" href="https://clinicaltrials.gov/ct2/show/NCT02315768">https://clinicaltrials.gov/ct2/show/NCT02315768</a>).
    Turrini, Mauro;
    Arcaini, Luca;
    Santini, Simone;
    Cerqueti, Manuela;
    Ferreri, Andres J. M.;
    Cantore, Nicola;
    Inzoli, Alessandro;
    Cardinale, Giovanni;
    Ronci, Benedetto;
    La Nasa, Giorgio;
    Massimi, Stefano;
    Gaglione, Gianfranco;
    Barbiero, Valentina;
    Martelli, Maurizio
    2022 Advances in Hematology

    doi: 10.1155/2022/5581772pmid: 35126524

    Subcutaneous (SC) rituximab may be beneficial in terms of convenience and tolerability, with potentially fewer and less severe administration-related reactions (ARRs) compared to the intravenous (IV) form. This report presents the results of a phase IIIb study conducted in Italy. The study included adult patients with CD20&#x2b; DLBCL or FL having received at least one full dose of IV RTX 375&#x2009;mg/m<sup>2</sup> during induction or maintenance. Patients on induction received &#x2265;4 cycles of RTX SC 1400&#x2009;mg plus standard chemotherapy and FL patients on maintenance received &#x2265;6 cycles of RTX SC. Overall, 159 patients (73 DLBCL, 86 FL) were enrolled: 103 (54 DLBCL, 49 FL) completed induction and 42 patients with FL completed 12 maintenance cycles. ARRs were reported in 10 patients (6.3&#x0025;), 3 (4.2&#x0025;) with DLBCL and 7 (8.1&#x0025;) with FL, all of mild severity, and resolved without dose delay/discontinuation. Treatment-emergent adverse events (TEAEs) and serious adverse events occurred in 41 (25.9&#x0025;) and 14 patients (8.9&#x0025;), respectively. Two patients with DLBCL had fatal events: <i>Klebsiella</i> infection (related to rituximab) and septic shock (related to chemotherapy). Neutropenia (14 patients, 8.9&#x0025;) was the most common treatment-related TEAE. Two patients with DLBCL (2.8&#x0025;) and 6 with FL (7.0&#x0025;) discontinued rituximab due to TEAEs. 65.2&#x0025; and 69.7&#x0025; of patients with DLBCL and 67.9&#x0025; and 73.6&#x0025; of patients with FL had complete response (CR) and CR unconfirmed, respectively. The median time to events (EFS, PFS, and OS) was not estimable due to the low rate of events. At a median follow-up of 29.5 and 47.8 months in patients with DLBCL and FL, respectively, EFS, PFS, and OS were 70.8&#x0025;, 70.8&#x0025;, and 80.6&#x0025; in patients with DLBCL and 77.9&#x0025;, 77.9&#x0025;, and 95.3&#x0025; in patients with FL, respectively. The switch from IV to SC rituximab in patients with DLBCL and FL was associated with low risk of ARRs and satisfactory response in both groups. This trial was registered with <a target="_blank" href="https://clinicaltrials.gov/ct2/show/NCT01987505">NCT01987505</a>.