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  1. Article: When can tyrosine kinase inhibitors be discontinued in patients with chronic myeloid leukemia?

    Mahon, Francois-Xavier

    Clinical advances in hematology & oncology : H&O

    2019  Volume 17, Issue 2, Page(s) 101–103

    MeSH term(s) Antineoplastic Agents/administration & dosage ; Antineoplastic Agents/adverse effects ; Antineoplastic Agents/therapeutic use ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Clinical Decision-Making ; Clinical Trials as Topic ; Disease Management ; Humans ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/diagnosis ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Protein Kinase Inhibitors/administration & dosage ; Protein Kinase Inhibitors/adverse effects ; Protein Kinase Inhibitors/therapeutic use ; Retreatment ; Time Factors ; Treatment Outcome
    Chemical Substances Antineoplastic Agents ; Protein Kinase Inhibitors
    Language English
    Publishing date 2019-03-07
    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: How to interpret the EURO-SKI study and its treatment-free remission outcome. Reply to R.P. Gale and J. Chen.

    Pfirrmann, Markus / Saussele, Susanne / Mahon, François-Xavier / Richter, Johan

    Leukemia

    2024  Volume 38, Issue 2, Page(s) 460–462

    Language English
    Publishing date 2024-01-03
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 807030-1
    ISSN 1476-5551 ; 0887-6924
    ISSN (online) 1476-5551
    ISSN 0887-6924
    DOI 10.1038/s41375-023-02124-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Treatment-free remission in CML: who, how, and why?

    Mahon, Francois-Xavier

    Hematology. American Society of Hematology. Education Program

    2017  Volume 2017, Issue 1, Page(s) 102–109

    Abstract: Chronic myeloid leukemia (CML) is the best example of successful targeted therapy. Today, the overall survival of patients with CML treated by using tyrosine kinase inhibitors (TKIs) is very close to that of the healthy population. The current question ... ...

    Abstract Chronic myeloid leukemia (CML) is the best example of successful targeted therapy. Today, the overall survival of patients with CML treated by using tyrosine kinase inhibitors (TKIs) is very close to that of the healthy population. The current question is: how can we further ameliorate the clinical outcome of patients with CML? Clinical trials have shown that some patients with CML in the chronic phase who achieve sustained deep molecular responses on TKI therapy can safely suspend therapy with no evidence of relapse. The long follow-up studies and the number of eligible patients have now validated the concept of treatment-free remission (ie, the ability to maintain a molecular response after stopping therapy). It should be considered as the future criterion to evaluate the success of clinical trials, especially if we want to take into account the quality of life of patients in addition to the economic aspect. Because post-TKI discontinuation follow-ups have been increasing over time with no evidence of relapse in some patients, the next step for the coming decade will be to address the topic of CML cure.
    MeSH term(s) Disease-Free Survival ; Humans ; Leukemia, Lymphocytic, Chronic, B-Cell/metabolism ; Leukemia, Lymphocytic, Chronic, B-Cell/mortality ; Quality of Life ; Remission, Spontaneous ; Survival Rate
    Language English
    Publishing date 2017-12-06
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 1520-4383
    ISSN (online) 1520-4383
    DOI 10.1182/asheducation-2017.1.102
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Discontinuation of TKI therapy and 'functional' cure for CML.

    Mahon, François-Xavier

    Best practice & research. Clinical haematology

    2016  Volume 29, Issue 3, Page(s) 308–313

    Abstract: Stopping tyrosine kinase inhibitor (TKI) therapy after achieving a sustained deep molecular response is an emerging treatment goal for patients with chronic myeloid leukaemia in chronic phase (CML-CP). Indeed, the feasibility of stopping TKI therapy has ... ...

    Abstract Stopping tyrosine kinase inhibitor (TKI) therapy after achieving a sustained deep molecular response is an emerging treatment goal for patients with chronic myeloid leukaemia in chronic phase (CML-CP). Indeed, the feasibility of stopping TKI therapy has been confirmed in various studies. The Stop Imatinib 1 (STIM1) study has shown a consistent follow-up which allowed defining a new criterion of clinical outcome evaluation, the treatment free remission (TFR). However, announcing a definitive cure remains a challenge owing to the discovery that TKIs spare quiescent leukaemic stem cells (LSC). It is definitely known that even a patient in long-term TFR has persistent LSCs. For this reason, a "functional" cure has been defined and proposed.
    MeSH term(s) Clinical Trials as Topic ; Humans ; Imatinib Mesylate/therapeutic use ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/enzymology ; Neoplastic Stem Cells/enzymology ; Protein Kinase Inhibitors/therapeutic use
    Chemical Substances Protein Kinase Inhibitors ; Imatinib Mesylate (8A1O1M485B)
    Language English
    Publishing date 2016-10-20
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 2048027-1
    ISSN 1532-1924 ; 1521-6926
    ISSN (online) 1532-1924
    ISSN 1521-6926
    DOI 10.1016/j.beha.2016.10.014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Discontinuation of tyrosine kinase therapy in CML.

    Mahon, Francois-Xavier

    Annals of hematology

    2015  Volume 94 Suppl 2, Page(s) S187–93

    Abstract: Over the past decade, a broad array of drugs designed to selectively inhibit protein tyrosine kinases (tyrosine kinase inhibitors or TKIs) have emerged as novel therapies for cancer patients. Chronic myeloid leukemia (CML) is one of the best examples of ... ...

    Abstract Over the past decade, a broad array of drugs designed to selectively inhibit protein tyrosine kinases (tyrosine kinase inhibitors or TKIs) have emerged as novel therapies for cancer patients. Chronic myeloid leukemia (CML) is one of the best examples of successful targeted therapy with a TKI. The overall survival of CML patients who respond to treatment is close to that of the healthy population. The response in many patients is so profound that it is possible to consider stopping their treatment and with time, the number of patients in this group has increased to the point where the issue of treatment cessation has become of utmost importance. This has led to the development of a new concept in the evaluation of CML entitled treatment-free remission. It will be the criterion to evaluate the success of future clinical trials, especially if we want to improve the management of the disease to the point where we can claim to have cured CML.
    MeSH term(s) Antineoplastic Agents/adverse effects ; Antineoplastic Agents/therapeutic use ; Drug Monitoring ; Fusion Proteins, bcr-abl/antagonists & inhibitors ; Humans ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/enzymology ; Maintenance Chemotherapy/adverse effects ; Molecular Targeted Therapy/adverse effects ; Practice Guidelines as Topic ; Precision Medicine ; Protein Kinase Inhibitors/adverse effects ; Protein Kinase Inhibitors/therapeutic use ; Remission Induction
    Chemical Substances Antineoplastic Agents ; BCR-ABL1 fusion protein, human ; Protein Kinase Inhibitors ; Fusion Proteins, bcr-abl (EC 2.7.10.2)
    Language English
    Publishing date 2015-04
    Publishing country Germany
    Document type Journal Article ; Review
    ZDB-ID 1064950-5
    ISSN 1432-0584 ; 0939-5555 ; 0945-8077
    ISSN (online) 1432-0584
    ISSN 0939-5555 ; 0945-8077
    DOI 10.1007/s00277-015-2320-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Treatment-Free Remission After Second-Line Nilotinib Treatment.

    Mahon, François-Xavier / Hughes, Timothy P

    Annals of internal medicine

    2018  Volume 169, Issue 7, Page(s) 510

    MeSH term(s) Humans ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive ; Pyrimidines
    Chemical Substances Pyrimidines ; nilotinib (F41401512X)
    Language English
    Publishing date 2018-08-16
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 336-0
    ISSN 1539-3704 ; 0003-4819
    ISSN (online) 1539-3704
    ISSN 0003-4819
    DOI 10.7326/L18-0431
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: No, treatment for CML should not continue indefinitely.

    Etienne, Gabriel / Mahon, François-Xavier

    Clinical advances in hematology & oncology : H&O

    2017  Volume 15, Issue 6, Page(s) 489–494

    MeSH term(s) Antineoplastic Agents/administration & dosage ; Humans ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Protein Kinase Inhibitors/administration & dosage
    Chemical Substances Antineoplastic Agents ; Protein Kinase Inhibitors
    Language English
    Publishing date 2017-07-27
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2271951-9
    ISSN 1543-0790
    ISSN 1543-0790
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: How I manage relapse of chronic myeloid leukaemia after stopping tyrosine kinase inhibitor therapy.

    Rea, Delphine / Mahon, François-Xavier

    British journal of haematology

    2017  

    Abstract: During the last 10 years, clinical trials formally demonstrated that about 50% of patients with chronic phase (CP) chronic myeloid leukaemia (CML) who achieve and maintain deep molecular responses for a prolonged period of time during treatment with ... ...

    Abstract During the last 10 years, clinical trials formally demonstrated that about 50% of patients with chronic phase (CP) chronic myeloid leukaemia (CML) who achieve and maintain deep molecular responses for a prolonged period of time during treatment with imatinib or new generation tyrosine kinase inhibitors (TKIs) may successfully stop their anti-leukaemic therapy. Based on the accumulated knowledge from abundant clinical trial experience, TKI discontinuation is becoming an important goal to achieve and is about to enter clinical practice. This review focuses on relapse definition, laboratory tests to identify relapse and relapse management after TKI discontinuation.
    Language English
    Publishing date 2017-10-19
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 80077-6
    ISSN 1365-2141 ; 0007-1048
    ISSN (online) 1365-2141
    ISSN 0007-1048
    DOI 10.1111/bjh.14973
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Is going for cure in chronic myeloid leukemia possible and justifiable?

    Mahon, François-Xavier

    Hematology. American Society of Hematology. Education Program

    2012  Volume 2012, Page(s) 122–128

    Abstract: After more than a decade of treatment of chronic myeloid leukemia (CML) patients with the BCR-ABL tyrosine kinase inhibitor imatinib, and despite the impressive clinical results of this targeted therapeutic, many questions remain unresolved. One major ... ...

    Abstract After more than a decade of treatment of chronic myeloid leukemia (CML) patients with the BCR-ABL tyrosine kinase inhibitor imatinib, and despite the impressive clinical results of this targeted therapeutic, many questions remain unresolved. One major question is how to cure CML, and the next step for the future will be to address this key issue. CML is a good model of cancer. The fact that the majority of CML patients who respond very well but discontinue tyrosine kinase inhibitors later show evidence of molecular recurrence focuses attention on the need for further research on leukemic stem cells. The challenge now is to understand why, after stopping treatment, the leukemia recurs in some patients but not in others. If we win this battle, this progress will certainly benefit the treatment and management of other leukemias and solid tumors and will validate this new topic.
    MeSH term(s) Antineoplastic Agents/therapeutic use ; Benzamides/therapeutic use ; Clinical Trials as Topic ; Fusion Proteins, bcr-abl/antagonists & inhibitors ; Humans ; Imatinib Mesylate ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/therapy ; Models, Theoretical ; Multicenter Studies as Topic ; Neoplastic Stem Cells/cytology ; Piperazines/therapeutic use ; Protein-Tyrosine Kinases/antagonists & inhibitors ; Pyrimidines/therapeutic use ; Recurrence ; Treatment Outcome
    Chemical Substances Antineoplastic Agents ; Benzamides ; Piperazines ; Pyrimidines ; Imatinib Mesylate (8A1O1M485B) ; Protein-Tyrosine Kinases (EC 2.7.10.1) ; Fusion Proteins, bcr-abl (EC 2.7.10.2)
    Language English
    Publishing date 2012
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 1520-4383
    ISSN (online) 1520-4383
    DOI 10.1182/asheducation-2012.1.122
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Kinetics of molecular recurrence after tyrosine kinase inhibitor cessation in chronic phase chronic myelogenous leukaemia patients.

    Alcazer, Vincent / Morisset, Stéphane / Rea, Delphine / Legros, Laurence / Dulucq, Stéphanie / Hayette, Sandrine / Cayuela, Jean-Michel / Huguet, Françoise / Mahon, François-Xavier / Etienne, Gabriel / Nicolini, Franck E

    British journal of haematology

    2024  Volume 204, Issue 4, Page(s) 1536–1539

    MeSH term(s) Humans ; Tyrosine Kinase Inhibitors ; Protein Kinase Inhibitors/therapeutic use ; Imatinib Mesylate ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy
    Chemical Substances Tyrosine Kinase Inhibitors ; Protein Kinase Inhibitors ; Imatinib Mesylate (8A1O1M485B)
    Language English
    Publishing date 2024-02-07
    Publishing country England
    Document type Letter
    ZDB-ID 80077-6
    ISSN 1365-2141 ; 0007-1048
    ISSN (online) 1365-2141
    ISSN 0007-1048
    DOI 10.1111/bjh.19330
    Database MEDical Literature Analysis and Retrieval System OnLINE

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