keyword
https://read.qxmd.com/read/34398511/safety-of-administration-of-bnt162b2-mrna-pfizer-biontech-covid-19-vaccine-in-youths-and-young-adults-with-a-history-of-acute-lymphoblastic-leukemia-and-allergy-to-peg-asparaginase
#21
JOURNAL ARTICLE
Catherine Mark, Sumit Gupta, Angela Punnett, Julia Upton, Julia Orkin, Adelle Atkinson, Lindsay Clarke, Alice Heisey, Christine McGovern, Sarah Alexander
Vaccinationis a critical tool in the prevention of COVID-19 infection for individuals and for communities. The mRNA vaccines contain polyethylene glycol (PEG) as a stabilizer. Currently, in North America, only the BNT162b2 (Pfizer-BioNTech) mRNA vaccine is approved for individuals aged 12-17. Most patients treated with contemporary regimens for acute lymphoblastic leukemia receive PEG-asparaginase (PEG-ASNase) and 10%-30% will develop allergic reactions. Optimizing access and safety for vaccine administration for these patients is critical...
November 2021: Pediatric Blood & Cancer
https://read.qxmd.com/read/34397119/lower-incidence-of-clinical-allergy-with-peg-asparaginase-upfront-versus-the-sequential-use-of-native-e-coli-asparaginase-followed-by-peg-asp-in-pediatric-patients-with-acute-lymphoblastic-leukemia
#22
JOURNAL ARTICLE
Montserrat Mesegué, Anna Alonso-Saladrigues, Sara Pérez-Jaume, Ariadna Comes-Escoda, José Luís Dapena, Anna Faura, Nuria Conde, Albert Català, Anna Ruiz-Llobet, Edgar Zapico-Muñiz, Mireia Camós, Susana Rives
Asparaginase (ASP) is an essential component for the acute lymphoblastic leukemia (ALL) treatment, but toxicities, such as allergy, frequently limit its use. Although the potentially lower PEG-ASP formulation immunogenicity, few studies with conflicting results have compared the allergy incidence between Escherichia coli-ASP and PEG-ASP in the same protocol. We aimed at comparing the allergy incidence in children receiving native E. coli-ASP versus PEG-ASP within the same clinical protocol (Spanish Society of Pediatric Hematology and Oncology ALL-SEHOP-PETHEMA 2013)...
August 16, 2021: Hematological Oncology
https://read.qxmd.com/read/34228505/efficacy-and-toxicity-of-pegaspargase-and-calaspargase-pegol-in-childhood-acute-lymphoblastic-leukemia-results-of-dfci-11-001
#23
RANDOMIZED CONTROLLED TRIAL
Lynda M Vrooman, Traci M Blonquist, Kristen E Stevenson, Jeffrey G Supko, Sarah K Hunt, Sarah M Cronholm, Victoria Koch, Samantha Kay-Green, Uma H Athale, Luis A Clavell, Peter D Cole, Marian H Harris, Kara M Kelly, Caroline Laverdiere, Jean-Marie Leclerc, Bruno Michon, Andrew E Place, Marshall A Schorin, Jennifer J G Welch, Donna S Neuberg, Stephen E Sallan, Lewis B Silverman
PURPOSE: Dana-Farber Cancer Institute Acute Lymphoblastic Leukemia (ALL) Consortium Protocol 11-001 assessed efficacy and toxicity of calaspargase pegol (calaspargase), a novel pegylated asparaginase formulation with longer half-life, compared with the standard formulation pegaspargase. METHODS: Patients age 1 to ≤ 21 years with newly diagnosed ALL or lymphoblastic lymphoma were randomly assigned to intravenous pegaspargase or calaspargase, 2,500 IU/m2 /dose. Patients received one induction dose...
November 1, 2021: Journal of Clinical Oncology
https://read.qxmd.com/read/33285386/role-of-phopr-in-the-response-to-stress-of-mycobacterium-bovis
#24
JOURNAL ARTICLE
Elizabeth A García, Federico C Blanco, Laura I Klepp, Adriana Pazos, Michael R McNeil, Mary Jackson, Fabiana Bigi
PhoP is part of the two-component PhoPR system that regulates the expression of virulence genes of Mycobacteria. The goal of this work was to elucidate the role of PhoP in the mechanism that Mycobacterium bovis, the causative agent of bovine tuberculosis, displays upon stress. An analysis of gene expression and acidic growth curves indicated that M. bovis neutralized the external acidic environment by inducing and secreting ammonia. We found that PhoP is essential for ammonia production/secretion and its role in this process seems to be the induction of asparaginase and urease expression...
November 21, 2020: Comparative Immunology, Microbiology and Infectious Diseases
https://read.qxmd.com/read/33217039/two-tagging-single-nucleotide-polymorphisms-to-capture-hla-drb1-07-01-dqa1-02-01-dqb1-02-02-haplotype-associated-with-asparaginase-hypersensitivity
#25
JOURNAL ARTICLE
Nóra Kutszegi, András Gézsi, Ágnes F Semsei, Judit Müller, Réka Simon, Erika Rozália Kovács, Katalin Hegedüs, Gábor T Kovács, Csaba Szalai, Dániel J Erdélyi
AIMS: Asparaginase (ASP) hypersensitivity is a well-known challenge in the treatment of lymphoblastic malignancies. In terms of cost considerations, the cheap native Escherichia coli ASP, the most immunogenic form of this medication, is used in the first line in middle-income countries. Previously, the role of the HLA-DRB1*07:01-DQA1*02:01-DQB1*02:02 haplotype had been established to associate with E. coli ASP hypersensitivity. We investigated a possible cost-effective genetic testing method to identify patients harbouring the risk HLA haplotype in order to pave the way for safer ASP treatment...
November 20, 2020: British Journal of Clinical Pharmacology
https://read.qxmd.com/read/32057100/prospective-real-time-monitoring-of-pegylated-escherichia-coli-and-erwinia-asparaginase-therapy-in-childhood-acute-lymphoblastic-leukaemia-and-non-hodgkin-lymphoma-in-belgium
#26
JOURNAL ARTICLE
Veerle Mondelaers, Alina Ferster, Anne Uyttebroeck, Bénédicte Brichard, Jutte van der Werff Ten Bosch, Koenraad Norga, Nadine Francotte, Caroline Piette, Katrien Vandemeulebroecke, Charlotte Verbeke, Susanne Schmidt, Yves Benoit, Tim Lammens, Barbara De Moerloose
Asparaginase (ASNase) is an important anti-leukaemic drug in the treatment of childhood acute lymphoblastic leukaemia (ALL) and non-Hodgkin lymphoma (NHL). A substantial proportion of patients develop hypersensitivity reactions with anti-ASNase neutralising antibodies, resulting in allergic reactions or silent inactivation (SI), and characterised by inactivation and rapid clearance of ASNase. We report results of a prospective, real-time therapeutic drug monitoring of pegylated Escherichia coli (PEG-)ASNase and Erwinia ASNase in children treated for ALL and NHL in Belgium...
July 2020: British Journal of Haematology
https://read.qxmd.com/read/31801703/asparaginase-an-old-drug-with-new-questions
#27
REVIEW
Daiane Keller Cecconello, Mariana Rodrigues de Magalhães, Isabel Cristina Ribas Werlang, Maria Lucia de Martino Lee, Mariana Bohns Michalowski, Liane Esteves Daudt
The long-term outcome of acute lymphoblastic leukemia has improved dramatically due to the development of more effective treatment strategies. L-asparaginase (ASNase) is one of the main drugs used and causes death of leukemic cells by systematically depleting the non-essential amino acid asparagine. Three main types of ASNase have been used so far: native ASNase derived from Escherichia coli, an enzyme isolated from Erwinia chrysanthemi and a pegylated form of the native E. coli ASNase, the ASNase PEG. Hypersensitivity reactions are the main complication related to this drug...
July 2020: Hematology, Transfusion and Cell Therapy
https://read.qxmd.com/read/31764026/study-of-l-asparaginase-vincristine-and-dexamethasone-combined-with-intensity-modulated-radiation-therapy-in-early-stage-nasal-nk-t-cell-lymphoma
#28
JOURNAL ARTICLE
Yunfei Hu, Mengxiang Chen, Yang Song, Xiaomei Liu, Feng Gou, Jing Zhang, Yunhong Huang
OBJECTIVES: Natural killer/T-cell lymphoma (NKTCL) is aggressive, and carries a poor prognosis worldwide. This retrospective study aimed to evaluate the clinical efficacy and safety of the LVD regimen (L-asparaginase, vincristine, and dexamethasone) combined with intensity-modulated radiation therapy (IMRT) for the treatment of early-stage nasal NKTCL in a Chinese population. METHODS: The clinical data were collected from patients treated between March 2010 and January 2017...
November 18, 2019: American Journal of Clinical Oncology
https://read.qxmd.com/read/31188727/antibodies-predict-pegaspargase-allergic-reactions-and-failure-of-rechallenge
#29
JOURNAL ARTICLE
Yiwei Liu, Colton A Smith, John C Panetta, Wenjian Yang, Lauren E Thompson, Jacob P Counts, Alejandro R Molinelli, Deqing Pei, Nancy M Kornegay, Kristine R Crews, Hope Swanson, Cheng Cheng, Seth E Karol, William E Evans, Hiroto Inaba, Ching-Hon Pui, Sima Jeha, Mary V Relling
PURPOSE: Pegaspargase (PEG-ASP) has largely replaced native Escherichia coli asparaginase (L-ASP) in the treatment of acute lymphoblastic leukemia because of its longer half-life and lower immunogenicity. Risk factors for allergic reactions to PEG-ASP remain unclear. Here, we identify risk factors for reactions in a front-line acute lymphoblastic leukemia trial and assess the usefulness of serum antibodies for diagnosing allergy and predicting rechallenge outcome. PATIENTS AND METHODS: PEG-ASP was administered to 598 patients in St Jude's Total XVI study...
August 10, 2019: Journal of Clinical Oncology
https://read.qxmd.com/read/31099289/a-single-center-multidisciplinary-approach-to-managing-the-global-erwinia-asparaginase-shortage
#30
JOURNAL ARTICLE
Bernard L Marini, Julia Brown, Lydia Benitez, Emily Walling, Raymond J Hutchinson, Rajen Mody, Rama Jasty Rao, Lynn Slagle, Lauren Bishop, Kristen Pettit, Dale L Bixby, Patrick W Burke, Anthony J Perissinotti
The availability of Erwinia Asparaginase has been limited across the world due to manufacturing shortages or for some countries due to the high acquisition cost, putting patients at risk for inferior outcomes. This manuscript provides guidance on how to manage hypersensitivity reactions and utilize therapeutic drug monitoring (TDM) to conserve and limit Erwinia use. The clinical and financial impact of a multidisciplinary committee are also discussed. Faced with a global Erwinia shortage, a multidisciplinary asparaginase allergy committee was created to review all hypersensitivity reactions to asparaginase therapy, staff education was performed on the management of asparaginase hypersensitivity reactions, an institution-wide premedication policy was mandated, and standardized guidelines were created for TDM...
December 2019: Leukemia & Lymphoma
https://read.qxmd.com/read/30826572/dynamic-changes-in-specific-anti-l-asparaginase-antibodies-generation-during-acute-lymphoblastic-leukemia-treatment
#31
JOURNAL ARTICLE
Justyna Walenciak, Krystyna Wyka, Szymon Janczar, Wojciech Młynarski, Beata Zalewska-Szewczyk
BACKGROUND: L-asparaginase (L-asp) remains one of the key components of acute lymphoblastic leukemia therapy. Immune reactions to the drug are associated with its diminished activity. The aim of the study was to determine the level of IgM, IgG and IgE-class anti-L-asp antibodies during the induction and reinduction phases of acute lymphoblastic leukemia therapy and their influence on L-asp activity. METHODS: The study group comprised 65 patients treated for acute lymphoblastic leukemia in one pediatric oncology center...
April 2019: Pharmacological Reports: PR
https://read.qxmd.com/read/30450575/genetic-predisposition-to-peg-asparaginase-hypersensitivity-in-children-treated-according-to-nopho-all2008
#32
MULTICENTER STUDY
Sofie G Højfeldt, Benjamin O Wolthers, Morten Tulstrup, Jonas Abrahamsson, Ramneek Gupta, Arja Harila-Saari, Mats Heyman, Louise T Henriksen, Òlafur G Jónsson, Päivi M Lähteenmäki, Bendik Lund, Kaie Pruunsild, Goda Vaitkeviciene, Kjeld Schmiegelow, Birgitte K Albertsen
Asparaginase is essential in childhood acute lymphoblastic leukaemia (ALL) treatment, however hypersensitivity reactions to pegylated asparaginase (PEG-asparaginase) hampers anti-neoplastic efficacy. Patients with PEG-asparaginase hypersensitivity have been shown to possess zero asparaginase enzyme activity. Using this measurement to define the phenotype, we investigated genetic predisposition to PEG-asparaginase hypersensitivity in a genome-wide association study (GWAS). From July 2008 to March 2016, 1494 children were treated on the Nordic Society of Paediatric Haematology and Oncology ALL2008 protocol...
February 2019: British Journal of Haematology
https://read.qxmd.com/read/29727043/efficacy-and-safety-of-recombinant-e-coli-asparaginase-in-children-with-previously-untreated-acute-lymphoblastic-leukemia-a-randomized-multicenter-study-of-the-dutch-childhood-oncology-group
#33
RANDOMIZED CONTROLLED TRIAL
Inge M van der Sluis, Hester de Groot-Kruseman, Maroeska Te Loo, Wim J E Tissing, Cor van den Bos, Gertjan J L Kaspers, Marc Bierings, Wouter J W Kollen, Thorsten König, Uwe Pichlmeier, Hans-Jürgen Kühnel, Rob Pieters
BACKGROUND: The efficacy and safety of recombinant Escherichia coli-asparaginase (rASNase) was compared to native E.coli asparaginase (Asparaginase medac). METHODS: One hundred and ninety-nine children with newly diagnosed acute lymphoblastic leukemia were randomized to receive one of both agents at a dose of 5,000 U/m² during induction (eight doses) and 10,000 U/m² during the postinduction phase (only high-risk patients; standard- and medium-risk patients received pegaspargase)...
August 2018: Pediatric Blood & Cancer
https://read.qxmd.com/read/29387211/a-retrospective-comparison-of-escherichia-coli-and-polyethylene-glycol-conjugated-asparaginase-for-the-treatment-of-adolescents-and-adults-with-newly-diagnosed-acute-lymphoblastic-leukemia
#34
JOURNAL ARTICLE
Jiabao Liang, Pengcheng Shi, Xutao Guo, Jie Li, Lingli He, Yan Wang, Qi Wei, Fen Huang, Zhiping Fan, Bing Xu
Data from clinical trials suggest that polyethylene glycol-conjugated asparaginase (PEG asparaginase) should be recommended as a replacement for Escherichia coli ( E. coli ) asparaginase in the treatment of pediatric acute lymphoblastic leukemia (ALL) due to its prolonged effect, similar safety profile and convenience. The present study investigated the efficacy and safety of PEG asparaginase in adolescents and adults with newly diagnosed ALL. The clinical data of 122 patients, ≥14 years old with de novo ALL, who received either PEG asparaginase or E...
January 2018: Oncology Letters
https://read.qxmd.com/read/28766887/a-cost-analysis-of-individualized-asparaginase-treatment-in-pediatric-acute-lymphoblastic-leukemia
#35
JOURNAL ARTICLE
Robin Q H Kloos, Carin A Uyl-de Groot, Raphaële R L van Litsenburg, Gertjan J L Kaspers, Rob Pieters, Inge M van der Sluis
BACKGROUND: Therapeutic drug monitoring (TDM) of asparaginase is necessary to respond to variability in asparaginase activity levels, detect silent inactivation, and distinguish between real allergies and allergic-like reactions with and without asparaginase neutralization, respectively. In this study, the costs of an individualized and fixed asparaginase dosing schedule were compared. PROCEDURE: Patients, treated according to the Dutch Childhood Oncology Group ALL-11 protocol (individualized PEGasparaginase treatment, starting dose: 1,500 IU/m2 ) or ALL-10 protocol (native Escherichia coli asparaginase followed by 2,500 IU/m2 PEGasparaginase), were included...
December 2017: Pediatric Blood & Cancer
https://read.qxmd.com/read/28751566/prolonged-versus-standard-native-e-coli-asparaginase-therapy-in-childhood-acute-lymphoblastic-leukemia-and-non-hodgkin-lymphoma-final-results-of-the-eortc-clg-randomized-phase-iii-trial-58951
#36
RANDOMIZED CONTROLLED TRIAL
Veerle Mondelaers, Stefan Suciu, Barbara De Moerloose, Alina Ferster, Françoise Mazingue, Geneviève Plat, Karima Yakouben, Anne Uyttebroeck, Patrick Lutz, Vitor Costa, Nicolas Sirvent, Emmanuel Plouvier, Martine Munzer, Maryline Poirée, Odile Minckes, Frédéric Millot, Dominique Plantaz, Philip Maes, Claire Hoyoux, Hélène Cavé, Pierre Rohrlich, Yves Bertrand, Yves Benoit
Asparaginase is an essential component of combination chemotherapy for childhood acute lymphoblastic leukemia and non-Hodgkin lymphoma. The value of asparaginase was further addressed in a group of non-very high-risk patients by comparing prolonged (long-asparaginase) versus standard (short-asparaginase) native E. coli asparaginase treatment in a randomized part of the phase III 58951 trial of the European Organization for Research and Treatment of Cancer Children's Leukemia Group. The main endpoint was disease-free survival...
October 2017: Haematologica
https://read.qxmd.com/read/28574850/whole-exome-sequencing-identified-genetic-risk-factors-for-asparaginase-related-complications-in-childhood-all-patients
#37
JOURNAL ARTICLE
Rachid Abaji, Vincent Gagné, Chang Jiang Xu, Jean-François Spinella, Francesco Ceppi, Caroline Laverdière, Jean-Marie Leclerc, Stephen E Sallan, Donna Neuberg, Jeffery L Kutok, Lewis B Silverman, Daniel Sinnett, Maja Krajinovic
Allergy, pancreatitis and thrombosis are common side-effects of childhood acute lymphoblastic leukemia (ALL) treatment that are associated with the use of asparaginase (ASNase), a key component in most ALL treatment protocols. Starting with predicted functional germline variants obtained through whole-exome sequencing (WES) data of the Quebec childhood ALL cohort we performed exome-wide association studies with ASNase-related toxicities. A subset of top-ranking variants was further confirmed by genotyping (N=302) followed by validation in an independent replication group (N=282); except for thrombosis which was not available for that dataset...
July 4, 2017: Oncotarget
https://read.qxmd.com/read/28440015/hypertriglyceridemia-during-asparaginase-treatment-in-children-with-acute-lymphoblastic-leukemia-correlates-with-antithrombin-activity-in-adolescents
#38
MULTICENTER STUDY
Lisa Persson, Arja Harila-Saari, Ida Hed Myrberg, Mats Heyman, Anna Nilsson, Susanna Ranta
BACKGROUND: Asparaginase (ASP) is a cornerstone in the treatment of acute lymphoblastic leukemia (ALL). It is also known for its ability to cause side effects, such as allergy and pancreatitis, as well as lipid and coagulation disturbances. The most important laboratory abnormalities are hypertriglyceridemia (HTG) and low antithrombin (AT). HTG is usually considered to be transient and benign in children with ALL, whereas low AT activity predisposes to thrombosis. Studies on the incidence and significance of HTG in children with ALL are scarce, and their findings have not always been congruent...
October 2017: Pediatric Blood & Cancer
https://read.qxmd.com/read/28244643/plasma-asparaginase-activity-asparagine-concentration-and-toxicity-after-administration-of-erwinia-asparaginase-in-children-and-young-adults-with-acute-lymphoblastic-leukemia-phase-i-ii-clinical-trial-in-japan
#39
MULTICENTER STUDY
Chitose Ogawa, Fumi Taguchi, Hiroaki Goto, Katsuyoshi Koh, Daisuke Tomizawa, Akira Ohara, Atsushi Manabe
BACKGROUND: A phase I/II study of Erwinia asparaginase in Japanese children and young adults with acute lymphoblastic leukemia (ALL) was performed to investigate its activity and toxicity. PROCEDURE: Eligible patients were in remission and had developed allergy to Escherichia coli asparaginase. Erwina asparaginase was intramuscularly administrated on days 2, 5, 7, 9, 11, and 13. To measure the plasma l-asparagine concentration (PAC), amino acids were derivatized with N(α) -(5-fluoro-2,4-dinitrophenyl)-l-leucinamide...
September 2017: Pediatric Blood & Cancer
https://read.qxmd.com/read/28096535/genetics-of-ancestry-specific-risk-for-relapse-in-acute-lymphoblastic-leukemia
#40
RANDOMIZED CONTROLLED TRIAL
S E Karol, E Larsen, C Cheng, X Cao, W Yang, L B Ramsey, C A Fernandez, J R McCorkle, S W Paugh, R J Autry, E Lopez-Lopez, B Diouf, S Jeha, C-H Pui, E A Raetz, N J Winick, W L Carroll, S P Hunger, M L Loh, M Devidas, W E Evans, J J Yang, M V Relling
The causes of individual relapses in children with acute lymphoblastic leukemia (ALL) remain incompletely understood. We evaluated the contribution of germline genetic factors to relapse in 2225 children treated on Children's Oncology Group trial AALL0232. We identified 302 germline single-nucleotide polymorphisms (SNPs) associated with relapse after adjusting for treatment and ancestry and 715 additional SNPs associated with relapse in an ancestry-specific manner. We tested for replication of these relapse-associated SNPs in external data sets of antileukemic drug pharmacokinetics and pharmacodynamics and an independent clinical cohort...
June 2017: Leukemia
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