Escalated daunorubicin dosing as an induction treatment for Philadelphia-negative adult acute lymphoblastic leukemia View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2013-08

AUTHORS

Sang Min Lee, Won Sik Lee, Ho Jin Shin, Je-Jung Lee, Sang Kyun Sohn, Joon Ho Moon, Hyeon Seok Eom, Jong Ho Won, Kyoo-Hyung Lee, Je-Hwan Lee, Dae-Young Kim, Sung-Soo Yoon, Inho Kim, Chul Won Jung, Seok Jin Kim, Hawk Kim, Jae Hoon Lee, Hun-Mo Ryoo, Gyeong-Won Lee, Sung-Hyun Kim, Yeung-Chul Mun, Min Kyoung Kim, Young Don Joo, The Korean Society of Hematology Adult ALL working party

ABSTRACT

The dose intensity of daunorubicin (DNR) delivered during the induction period represented the major prognostic factor for the outcome of adult acute lymphoblastic leukemia (ALL). The aim of this study was to determine the survival or toxicity of escalated doses of DNR in induction treatment of adult patients with acute lymphoblastic leukemia who are at least 15 years of age. For induction chemotherapy, all patients were given 90 mg/m(2)/day of DNR by continuous intravenous (IV) infusion over 24 h daily on days 1-3, 2 mg of vincristine IV push on days 1 and 8, and 60 mg/m(2)/day of prednisolone per oral (PO) on days 1-14 in conjunction with 4,000 units/m(2)/day of L-asparaginase intramuscular or subcutaneous on days 17-28. The median patient age was 32 years (range, 15-69). Complete remission (CR) was achieved in 169 (88.5 %) patients, while 4 died before CR was reached. Additionally, 11 patients died from leukemia progression, 4 had refractory disease, and 3 had follow-up loss. The median follow-up time was 697 days (range, 12-2,270). The 3-year cumulative incidence of relapse was 49.3 %. The probabilities of disease-free survival and overall survival at 3 years were 46.1 and 43.1 %, respectively. The dose of DNR was 100 % of the target dose, and there were no additional specific toxicities. The results show that escalated doses of DNR in induction chemotherapy are similar with the standard dose in response and toxicities. Our study indicates that a more effective regimen or better chemotherapy agents are needed to improve the CR rate and prolong survival in Philadelphia-negative adult ALL. More... »

PAGES

1101-1110

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00277-013-1728-y

DOI

http://dx.doi.org/10.1007/s00277-013-1728-y

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1042025872

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/23558905


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