Safety and efficacy of azacitidine in the treatment of elderly patients with myelodysplastic syndrome
被引:14
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作者:
Ritchie, Ellen K.
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机构:
Cornell Univ, New York Presbyterian Hosp, Weill Med Coll, New York, NY 10065 USA
Cornell Univ, Leukemia Program, Weill Med Coll, New York, NY 10065 USACornell Univ, New York Presbyterian Hosp, Weill Med Coll, New York, NY 10065 USA
Ritchie, Ellen K.
[1
,2
]
机构:
[1] Cornell Univ, New York Presbyterian Hosp, Weill Med Coll, New York, NY 10065 USA
[2] Cornell Univ, Leukemia Program, Weill Med Coll, New York, NY 10065 USA
The goals of treating older patients with myelodysplastic syndrome (MDS) are different than for younger patients. Few elderly patients are able to pursue an allogeneic stem cell transplant for potential cure of the disease. The focus for the treatment of older patients with MDS is therefore not curative, but rather alleviation of symptoms, improvement in quality of life, maintenance or improvement of functional status, and continued independent living. Prolongation of survival is only important if functional status and quality of life can be maintained, and there is greater risk of losing these outcomes in elderly patients. Azacitidine is an important drug for the treatment of older patients with MDS. Data from the AZA-001 trial has shown a survival benefit for patients with high-risk disease treated with azacitidine. Importantly, treatment has also been shown to improve quality of life for MDS patients. Subset analysis of the data has shown that the drug can be used safely in even the oldest patients with MDS and is superior to treatment with other established regimens, such as low-dose cytarabine. Given the delay between the initiation of treatment and the clinical response, patients may need aggressive supportive care with antiemetics, prophylactic antibiotics, and transfusions to maintain them through therapy. Azacitidine provides a better quality of response when it is used beyond the first response, so ongoing treatment is generally recommended in responding patients. A new oral preparation of the drug is in development that will make the treatment more feasible and comfortable for elderly patients.
机构:
China Med Univ Hosp, Dept Internal Med, Div Hematol & Oncol, Taichung 404, TaiwanChina Med Univ Hosp, Dept Internal Med, Div Hematol & Oncol, Taichung 404, Taiwan
Lin, Che-Hung
Yeh, Su-Peng
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China Med Univ Hosp, Dept Internal Med, Div Hematol & Oncol, Taichung 404, Taiwan
China Med Univ Hosp, Dept Med Res, Stem Cell Res Lab, Taichung 404, Taiwan
China Med Univ, Taichung 404, TaiwanChina Med Univ Hosp, Dept Internal Med, Div Hematol & Oncol, Taichung 404, Taiwan
Yeh, Su-Peng
Lin, Tze-Yi
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China Med Univ Hosp, Dept Internal Med, Div Hematol & Oncol, Taichung 404, TaiwanChina Med Univ Hosp, Dept Internal Med, Div Hematol & Oncol, Taichung 404, Taiwan
机构:
Univ Paris 13, Hop Avicenne, AP HP, Serv Hematol Clin, F-93009 Bobigny, FranceUniv Paris 13, Hop Avicenne, AP HP, Serv Hematol Clin, F-93009 Bobigny, France
Ades, Lionel
Itzykson, Raphael
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Univ Paris 13, Hop Avicenne, AP HP, Serv Hematol Clin, F-93009 Bobigny, FranceUniv Paris 13, Hop Avicenne, AP HP, Serv Hematol Clin, F-93009 Bobigny, France
机构:
US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Kaminskas, E
Farrell, A
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Farrell, A
Abraham, S
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Abraham, S
Baird, A
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Baird, A
Hsieh, LS
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Hsieh, LS
Lee, SL
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Lee, SL
Leighton, JK
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Leighton, JK
Patel, H
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Patel, H
Rahman, A
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Rahman, A
Sridhara, R
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Sridhara, R
Wang, YC
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA
Wang, YC
Pazdur, R
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US FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USAUS FDA, Ctr Drug Evaluat & Res, Div Oncol Drug Prod, Rockville, MD 20857 USA