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  1. NTU Scholars
  2. 醫學院
  3. 醫學系
Please use this identifier to cite or link to this item: https://scholars.lib.ntu.edu.tw/handle/123456789/537540
Title: Philadelphia chromosome-positive acute lymphoblastic leukemia in Taiwan
Authors: BOR-SHENG KO 
JIH-LUH TANG 
Tsai W.
YAO-CHANG CHEN 
Wang C.-H.
Sheng M.-C.
Lin D.-T.
Lin K.-H.
HWEI-FANG TIEN 
Issue Date: 2001
Journal Volume: 80
Journal Issue: 9
Start page/Pages: 510-515
Source: Annals of Hematology
Abstract: 
From January 1986 to December 1998, 26 (23%) of 114 acute lymphoblastic leukemia (ALL) patients older than 15 years were found to have Philadelphia (Ph) chromosome. They accounted for 28% (26 of 94) of the patients with B-lineage ALL. Compared with the other 88 ALL patients, the leukemic cells from all but one Ph-positive ALL patients were early pre-B cells with a higher rate of CD34 expression (92% vs 50%, P<0.05). At presentation, the Ph-positive adult ALL patients had higher circulating blasts (mean 21.4 vs 3.66x104/μl, P<0.05) and lower initial platelet counts (mean 4.47 vs 7.34x104/μl, P<0.01) and showed a trend toward higher frequency of initial central nerve system (CNS) involvement (25% vs 11%, P=0.098) than the others. Among patients with adequate chemotherapy, 16 (64%) of the 25 Ph-positive ALL patients achieved complete remission (CR), an incidence marginally lower than that of Ph-negative ALL (62 of 76, 82%, P=0.06) and significantly lower than that of Ph-negative B-lineage ALL (50 of 58, 86%, P=0.0037). However, all patients relapsed except for those who received allogeneic hemopoietic stem cell transplantation (allo-HSCT). The probabilities of 5-year continuous CR and 5-year survival for Ph-positive adult ALL patients were significantly inferior to those for Ph-negative adult ALL patients (0% vs 12%, P=0.0001, and 7% vs 19%, P=0.047, respectively), and those for Ph-negative B-lineage ALL (0% vs 14%, P<0.0001, and 7% vs 23%, P=0.002, respectively). Prognostic factors were analyzed among the Ph-positive ALL patients including the 26 adults mentioned above and an additional 11 children. No clinical or biological characteristics such as age, sex, initial circulating blast count, extramedullary involvement, or CD34 expression had an impact on the disease outcome. Allo-HSCT in first CR may improve the probability of 5-year continuous CR (100% vs. 0% for those without allo-HSCT, P=0.0091) although only three patients received it in this study. In conclusion, Ph-positive ALL patients tended to have a poor prognosis, regardless of whether other possible risk factors were present or not. Aggressive treatment, such as high-dose chemotherapy with allo-HSCT, should be considered for these patients to improve survival.
URI: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034794596&doi=10.1007%2fs002770100338&partnerID=40&md5=4b3d7b7892a40587d535c471fbb8eca2
https://scholars.lib.ntu.edu.tw/handle/123456789/537540
ISSN: 0939-5555
DOI: 10.1007/s002770100338
SDG/Keyword: anthracycline; antileukemic agent; antineoplastic agent; asparaginase; BCR ABL protein; CD19 antigen; CD2 antigen; CD20 antigen; CD3 antigen; CD34 antigen; CD4 antigen; CD5 antigen; CD7 antigen; CD8 antigen; common acute lymphoblastic leukemia antigen; cyclophosphamide; cytarabine; etoposide; gene product; hemoglobin; HLA DR antigen; lymphocyte membrane immunoglobulin; mercaptopurine; methotrexate; monoclonal antibody; prednisolone; protein tyrosine kinase; T lymphocyte antigen; unindexed drug; vincristine; acute lymphoblastic leukemia; adolescent; adult; age; aged; allogenic bone marrow transplantation; antigen expression; article; B cell leukemia; blast cell; cancer combination chemotherapy; cancer diagnosis; cancer recurrence; cancer survival; cell lineage; central nervous system disease; chromosome analysis; clinical trial; controlled clinical trial; controlled study; dose response; drug megadose; extramedullary hematopoiesis; female; hematopoietic stem cell transplantation; human; human cell; leukemia cell line; leukemia remission; major clinical study; male; Philadelphia 1 chromosome; pre B lymphocyte; priority journal; prognosis; risk factor; sex difference; Taiwan; thrombocyte count; treatment outcome; treatment planning; Adolescent; Adult; Aged; Female; Humans; Leukemia, Lymphocytic, Acute; Male; Middle Aged; Philadelphia Chromosome; Prognosis; Taiwan
[SDGs]SDG3
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