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  1. Article: Hyper-CVAD-based regimens in adult patients with acute lymphoblastic leukemia.

    Jabbour, Elias J

    Clinical advances in hematology & oncology : H&O

    2022  Volume 20, Issue 9, Page(s) 547–549

    MeSH term(s) Adult ; Humans ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; Vincristine
    Chemical Substances Vincristine (5J49Q6B70F)
    Language English
    Publishing date 2022-04-04
    Publishing country United States
    Document type Interview
    ZDB-ID 2271951-9
    ISSN 1543-0790
    ISSN 1543-0790
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Inotuzumab in Older Patients with Newly Diagnosed Acute Lymphoblastic Leukemia-A Podcast.

    Jabbour, Elias J / Stelljes, Matthias

    Targeted oncology

    2024  Volume 19, Issue 2, Page(s) 135–141

    Abstract: Older patients with acute lymphoblastic leukemia (ALL) have historically had poor outcomes (5-year survival rate, 20%) with standard intensive and dose-adjusted chemotherapy regimens, due to a high incidence of adverse biologic features including high- ... ...

    Abstract Older patients with acute lymphoblastic leukemia (ALL) have historically had poor outcomes (5-year survival rate, 20%) with standard intensive and dose-adjusted chemotherapy regimens, due to a high incidence of adverse biologic features including high-risk cytogenetics, presence of TP53 mutations, and poor tolerance to intensive therapy. Thus, there is an unmet medical need in this patient population. Inotuzumab ozogamicin is a humanized antibody-drug conjugate that targets CD22-positive leukemic blasts. It is approved for the treatment of relapsed or refractory ALL and has been shown to be effective and tolerable in older patients. Several ongoing trials in older patients with newly diagnosed ALL have yielded encouraging data with inotuzumab ozogamicin in induction alone and in combination with low-intensity chemotherapy. In this podcast, the authors summarize and highlight some of the recent findings on the use of inotuzumab ozogamicin as induction therapy for older adults with newly diagnosed ALL.
    MeSH term(s) Humans ; Aged ; Inotuzumab Ozogamicin/pharmacology ; Inotuzumab Ozogamicin/therapeutic use ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; Antibodies, Monoclonal, Humanized/adverse effects
    Chemical Substances Inotuzumab Ozogamicin (P93RUU11P7) ; Antibodies, Monoclonal, Humanized
    Language English
    Publishing date 2024-03-08
    Publishing country France
    Document type Letter
    ZDB-ID 2222136-0
    ISSN 1776-260X ; 1776-2596
    ISSN (online) 1776-260X
    ISSN 1776-2596
    DOI 10.1007/s11523-023-01023-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book: Optimizing tyrosine kinase inhibitor therapy in chronic myeloid leukemia

    Jabbour, Elias / Talpaz, Moshe

    a new era

    (Clinical lymphoma & myeloma ; 8, Suppl. 3)

    2008  

    Author's details suppl. ed.: Moshe Talpaz. Contributors Elias Jabbour
    Series title Clinical lymphoma & myeloma ; 8, Suppl. 3
    Collection
    Language English
    Size S. S69 - S117 : Ill., graph. Darst.
    Publisher CIG Media Group
    Publishing place Dallas, Tex
    Publishing country United States
    Document type Book
    HBZ-ID HT015540549
    Database Catalogue ZB MED Medicine, Health

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  4. Book: Unmet needs in the management of chronic myelogenous leukemia

    Jabbour, Elias / Bixby, Dale / Akard, Luke P.

    (Clinical advances in hematology & oncology ; 10,12, Suppl. 22)

    2012  

    Author's details discussants Elias J. Jabbour ; Dale Bixby ; Luke P. Akard
    Series title Clinical advances in hematology & oncology ; 10,12, Suppl. 22
    Collection
    Language English
    Size 15 S. : Ill., graph. Darst.
    Publisher Millennium Med. Publ
    Publishing place New York, NY
    Publishing country United States
    Document type Book
    HBZ-ID HT017526668
    Database Catalogue ZB MED Medicine, Health

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  5. Article ; Online: SOHO State of the Art Updates and Next Questions, Measurable Residual Disease in Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia.

    Short, Nicholas J / Jabbour, Elias / Kantarjian, Hagop

    Clinical lymphoma, myeloma & leukemia

    2024  

    Abstract: Assessment of measurable residual disease (MRD) provides important prognostic information and can inform decision-making about appropriate consolidative therapy in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL). ... ...

    Abstract Assessment of measurable residual disease (MRD) provides important prognostic information and can inform decision-making about appropriate consolidative therapy in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL). Many contemporary treatment protocols for Ph+ ALL achieve high rates of MRD negativity, and several analyses suggest that allogeneic hematopoietic stem cell transplant in first remission can be safely deferred in most patients who achieve MRD negativity by PCR for BCR::ABL1 within 3 months. Given the close association between achievement of MRD negativity and favorable long-term outcomes in Ph+ ALL, MRD response rates may aid in the evaluation of novel regimens, particularly in the absence of randomized data or robust survival data. While most studies in Ph+ ALL have used PCR for BCR::ABL1 to measure MRD and correlate with outcomes, this assay has several limitations. PCR or next-generation sequencing-based assays for immunoglobin or T-cell receptor (IG/TR) gene rearrangements may provide a more accurate assessment of clinically significant MRD in Ph+ ALL, particularly in patients with multilineage involvement of BCR::ABL1. Herein, we discuss the prognostic and therapeutic role of MRD in Ph+ ALL. We review the available methods of MRD assessment in Ph+ ALL and discuss the advantages of MRD assays that track IG/TR rearrangements rather than BCR::ABL1.
    Language English
    Publishing date 2024-02-21
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2540992-X
    ISSN 2152-2669 ; 2152-2650
    ISSN (online) 2152-2669
    ISSN 2152-2650
    DOI 10.1016/j.clml.2024.02.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: SOHO State of the Art Updates and Next Questions | Novel Agents and the Diminishing Role of Allogeneic Stem Cell Transplant in B-Acute Lymphoblastic Leukemia.

    Jen, Wei-Ying / Jabbour, Elias / Kantarjian, Hagop M / Short, Nicholas J

    Clinical lymphoma, myeloma & leukemia

    2024  

    Abstract: Outcomes of patients with B-acute lymphoblastic leukemia (B-ALL) have improved remarkably in the past decade. This has largely been due to the development and introduction of novel immunotherapies such as blinatumomab, inotuzumab ozogamicin, chimeric ... ...

    Abstract Outcomes of patients with B-acute lymphoblastic leukemia (B-ALL) have improved remarkably in the past decade. This has largely been due to the development and introduction of novel immunotherapies such as blinatumomab, inotuzumab ozogamicin, chimeric antigen receptor T (CAR-T) cells, highly potent tyrosine kinase inhibitors, and improved risk stratification, including better understanding of high risk genomic subgroups and better methods of measurable residual disease (MRD) detection. Historically, allogeneic stem cell transplant (allo-SCT) has been the consolidative treatment of choice in first complete remission for fit adults with B-ALL. However, allo-SCT is associated with significant treatment-related mortality and morbidity. Current research is directed at the incorporation of novel immunotherapies into frontline regimens to improve depth and durability of responses and ultimately increase cure rates. In this review, we will discuss the emerging role of novel immune-based treated strategies in both the frontline and relapsed/refractory settings. We present our approach to newly diagnosed patients with B-ALL and illustrate how the incorporation of novel agents and use of high-sensitivity MRD assays can abrogate the need for allo-SCT in most patients with B-ALL.
    Language English
    Publishing date 2024-03-06
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2540992-X
    ISSN 2152-2669 ; 2152-2650
    ISSN (online) 2152-2669
    ISSN 2152-2650
    DOI 10.1016/j.clml.2024.02.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: SOHO State of the Art Updates and Next Questions | Hyper-CVAD in 2022: Lessons Learned and New Approaches.

    Rausch, Caitlin R / Kantarjian, Hagop M / Jabbour, Elias J

    Clinical lymphoma, myeloma & leukemia

    2023  Volume 23, Issue 4, Page(s) 238–243

    Abstract: Combination chemotherapy is the mainstay of treatment for acute lymphoblastic leukemia (ALL). The Hyper-CVAD regimen was developed in 1992 at MD Anderson Cancer Center and has since become a standard of care option for adult patients with ALL. Since its ... ...

    Abstract Combination chemotherapy is the mainstay of treatment for acute lymphoblastic leukemia (ALL). The Hyper-CVAD regimen was developed in 1992 at MD Anderson Cancer Center and has since become a standard of care option for adult patients with ALL. Since its conception, a number of modifications have been implemented to customize the regimen for different patient populations and safely incorporate novel therapies without compromising tolerability. We aim to review the evolution of the Hyper-CVAD regimen over the past 3 decades, focusing on clinical pearls, as well as future directions.
    MeSH term(s) Adult ; Humans ; Doxorubicin/therapeutic use ; Cyclophosphamide/therapeutic use ; Retrospective Studies ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; Dexamethasone/therapeutic use ; Vincristine/therapeutic use
    Chemical Substances Doxorubicin (80168379AG) ; Cyclophosphamide (8N3DW7272P) ; Dexamethasone (7S5I7G3JQL) ; Vincristine (5J49Q6B70F)
    Language English
    Publishing date 2023-02-01
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2540992-X
    ISSN 2152-2669 ; 2152-2650
    ISSN (online) 2152-2669
    ISSN 2152-2650
    DOI 10.1016/j.clml.2023.01.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: An Update on the Management of Advanced Phase Chronic Myeloid Leukemia.

    Short, Nicholas J / Senapati, Jayastu / Jabbour, Elias

    Current hematologic malignancy reports

    2023  Volume 18, Issue 6, Page(s) 234–242

    Abstract: Purpose of review: While most patients with chronic myeloid leukemia (CML) present in a chronic phase and are expected to have a normal life expectancy, some patients present with or progress to a more aggressive accelerated phase (AP) or blast phase ( ... ...

    Abstract Purpose of review: While most patients with chronic myeloid leukemia (CML) present in a chronic phase and are expected to have a normal life expectancy, some patients present with or progress to a more aggressive accelerated phase (AP) or blast phase (BP) of CML. Herein, we discuss the diagnostic considerations of advanced phase CML and review its contemporary management.
    Recent findings: Later-generation, more potent BCR::ABL1 tyrosine kinase inhibitors (TKIs) such as ponatinib may result in superior outcomes in patients with advanced phase CML. For CML-BP, combination approaches directed against the blast immunophenotype appear superior to TKI monotherapy. The role of allogeneic stem cell transplantation is controversial in CML-AP but has consistently been shown to improve outcomes for patients with CML-BP. Advanced phase CML, particularly CML-BP, remains a poor risk subtype of CML. However, novel combination approaches using later-generation TKIs are being explored in clinical trials and may lead to improved outcomes.
    MeSH term(s) Humans ; Protein Kinase Inhibitors/adverse effects ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/diagnosis ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Blast Crisis/drug therapy ; Hematopoietic Stem Cell Transplantation ; Fusion Proteins, bcr-abl/genetics ; Drug Resistance, Neoplasm/genetics
    Chemical Substances Protein Kinase Inhibitors ; Fusion Proteins, bcr-abl (EC 2.7.10.2)
    Language English
    Publishing date 2023-08-31
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2229765-0
    ISSN 1558-822X ; 1558-8211
    ISSN (online) 1558-822X
    ISSN 1558-8211
    DOI 10.1007/s11899-023-00709-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: A Review of the Therapeutic Role of Bosutinib in Chronic Myeloid Leukemia.

    Kantarjian, Hagop M / Jabbour, Elias J / Lipton, Jeffrey H / Castagnetti, Fausto / Brümmendorf, Tim H

    Clinical lymphoma, myeloma & leukemia

    2024  Volume 24, Issue 5, Page(s) 285–297

    Abstract: The development of the BCR::ABL1 tyrosine kinase inhibitors (TKIs) has transformed Philadelphia chromosome (Ph)-positive chronic myeloid leukemia (CML) from a fatal disease to an often-indolent illness that, when managed effectively, can restore a life ... ...

    Abstract The development of the BCR::ABL1 tyrosine kinase inhibitors (TKIs) has transformed Philadelphia chromosome (Ph)-positive chronic myeloid leukemia (CML) from a fatal disease to an often-indolent illness that, when managed effectively, can restore a life expectancy close to that of the normal population. Bosutinib is a second-generation TKI approved for adults with Ph-positive CML in chronic phase, accelerated phase, or blast phase that is resistant or intolerant to prior therapy, and for newly diagnosed Ph-positive chronic phase CML. This review details the efficacy of bosutinib for the treatment of CML in the first- and second-line settings, as well as in third- and later-line settings for high-risk patients resistant or intolerant to at least 2 TKIs. It also outlines bosutinib studies that provide evidence for dose-optimization strategies that can be used to improve efficacy and effectively manage adverse events. The studies that provide evidence for specific patient populations benefiting particularly from bosutinib dose-optimization strategies are also discussed. The well-established, long-term side-effect profile and the potential to make dose adjustments with bosutinib make it an appropriate treatment option for patients with CML. Bosutinib has demonstrated a positive impact on health-related quality of life and an important role in the long-term treatment of patients with CML.
    MeSH term(s) Humans ; Aniline Compounds/therapeutic use ; Aniline Compounds/pharmacology ; Nitriles/therapeutic use ; Nitriles/pharmacology ; Quinolines/therapeutic use ; Quinolines/pharmacology ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Protein Kinase Inhibitors/therapeutic use ; Protein Kinase Inhibitors/pharmacology ; Antineoplastic Agents/therapeutic use ; Antineoplastic Agents/pharmacology ; Treatment Outcome
    Chemical Substances bosutinib (5018V4AEZ0) ; Aniline Compounds ; Nitriles ; Quinolines ; Protein Kinase Inhibitors ; Antineoplastic Agents
    Language English
    Publishing date 2024-01-12
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2540992-X
    ISSN 2152-2669 ; 2152-2650
    ISSN (online) 2152-2669
    ISSN 2152-2650
    DOI 10.1016/j.clml.2024.01.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Intensive Versus Non-Intensive Approach to Adults with Ph+ ALL: An Intensive Approach Is Still Standard of Care.

    Short, Nicholas J / Jabbour, Elias

    Clinical lymphoma, myeloma & leukemia

    2020  Volume 20 Suppl 1, Page(s) S52–S53

    MeSH term(s) Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Humans ; Philadelphia Chromosome ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; Standard of Care ; Survival Analysis
    Language English
    Publishing date 2020-08-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2540992-X
    ISSN 2152-2669 ; 2152-2650
    ISSN (online) 2152-2669
    ISSN 2152-2650
    DOI 10.1016/S2152-2650(20)30460-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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