Treatment of blastic phase chronic myeloid leukemia with mitoxantrone, cytosine arabinoside and high dose methylprednisolone

Autor: Mehmet H. Koseoglu, Hulki Meltem Sönmez, Ekrem Muftuoglu, Gurhan Kadikoylu, Süleyman Demir, Orhan Ayyildiz, Zahit Bolaman
Rok vydání: 2002
Předmět:
Male
drug megadose
age distribution
diarrhea
leukemia remission
rash
Gastroenterology
etoposide
hydroxyurea
granulocyte colony stimulating factor
cause of death
flushing
cytarabine
dose response
Streptococcus infection
neurotoxicity
Antineoplastic Combined Chemotherapy Protocols
conjunctivitis
Blastic phase
fever
clinical article
liver dysfunction
adult
Remission Induction
article
Cytarabine
prednisolone
Combination chemotherapy
clinical trial
Hematology
Middle Aged
alpha interferon
female
Treatment Outcome
carboplatin
Vomiting
mucosa inflammation
Female
medicine.symptom
Chronic myelogenous leukemia
medicine.drug
blast cell crisis
Adult
medicine.medical_specialty
azacitidine
Leukemia
Myeloid
Chronic

Nausea
cladribine
Blastic Phase
vincristine
Methylprednisolone
mitoxantrone
bone marrow hypoplasia
meprednisone
chronic myeloid leukemia
Internal medicine
Leukemia
Myelogenous
Chronic
BCR-ABL Positive

medicine
pneumonia
Humans
controlled study
human
bacteremia
survival time
lung toxicity
Mitoxantrone
controlled clinical trial
business.industry
5 aza 2' deoxycytidine
leukopenia
fludarabine
Philadelphia 1 chromosome
medicine.disease
Survival Analysis
Surgery
Regimen
febrile neutropenia
imatinib
High dose methylprednisolone
validation process
Blastic phase chronic myelogenous leukemia
nausea and vomiting
prognosis
business
Blast Crisis
drug tolerability
Zdroj: Haematologia. 32(1)
ISSN: 0017-6559
Popis: Fourteen patients with blastic phase chronic myelogenous leukemia received combination chemotherapy with mitoxantrone 5 mg/m2 intravenously daily for 3 days, cytosine arabinoside 100 mg/m2 intravenously over 2 hours bid for 7 days and high dose methylprednisolone 1000 mg/day intravenously for 5 days. The patients' mean age was 52 +/- 10 (range 34-64) and Philadelphia chromosome was positive in all. Five patients (35%) achieved complete remission and four patients (28%) had a partial remission. Overall remission rate was 64%. The mean survival was 11.1 +/- 8.6 months (median 13) for all patients, 19.4 +/- 4.0 months (median 19) for those achieving a complete remission, 12.50 +/- 5.7 months (median 14) for patients with partial remission and 1.8 +/- 1.8 months (median 2) for the unresponsive patients. Two of 5 unresponsive patients died early after the second course of remission induction. The treatment regimen was generally well tolerated. Marrow hypoplasia was observed in 9 (64%) patients and 7 (50%) had febrile episodes. Non-myelosupressive toxicity of the regimen was acceptable. Nausea and vomiting were observed in 8 (57%) patients and 3 (21%) patients developed flushing due to cytosine arabinoside. These results suggest that the regimen with mitoxantrone, cytosine arabinoside and high dose methylprednisolone in remission-induction of blastic phase chronic myelogenous leukemia may be a valid option that may also improve overall prognosis.
Databáze: OpenAIRE