Cargando…
High-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study.
In a single centre, 52 newly diagnosed patients with acute myeloid leukemia (AML) under the age of 56 years received induction chemotherapy commencing with high-dose cytosine arabinoside (Ara-C) and etoposide (Protocol BF11), followed by Ara-C, 6 thioguanine (6TG). A total of 67% of patients entered...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1990
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971542/ https://www.ncbi.nlm.nih.gov/pubmed/2245176 |
_version_ | 1782134932912472064 |
---|---|
author | Parikh, P. Powles, R. Treleaven, J. Helenglass, G. Gore, M. Rose, M. Talbot, D. Milan, S. Smith, C. Pinkerton, R. |
author_facet | Parikh, P. Powles, R. Treleaven, J. Helenglass, G. Gore, M. Rose, M. Talbot, D. Milan, S. Smith, C. Pinkerton, R. |
author_sort | Parikh, P. |
collection | PubMed |
description | In a single centre, 52 newly diagnosed patients with acute myeloid leukemia (AML) under the age of 56 years received induction chemotherapy commencing with high-dose cytosine arabinoside (Ara-C) and etoposide (Protocol BF11), followed by Ara-C, 6 thioguanine (6TG). A total of 67% of patients entered remission using these drugs. An anthracycline was added for those patients not in remission. The overall remission rate (CR) was 86.5% (45/52), with a minimum follow-up of 90 days. Patients are hospitalised for relatively short periods, and consequently require less blood product and antibiotic support. Patients in continuing first remission following induction with Ara-C and etoposide are similar in number to those in continuing first remission who initially received an anthracycline. This would imply that the efficiency of Ara-C and etoposide in inducing long-term disease-term survival is comparable with anthracycline-containing regimens. We conclude that high-dose Ara-C and etoposide used in the first induction cycle for treating AML have good antileukaemic effect with acceptable toxicity. |
format | Text |
id | pubmed-1971542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1990 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19715422009-09-10 High-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study. Parikh, P. Powles, R. Treleaven, J. Helenglass, G. Gore, M. Rose, M. Talbot, D. Milan, S. Smith, C. Pinkerton, R. Br J Cancer Research Article In a single centre, 52 newly diagnosed patients with acute myeloid leukemia (AML) under the age of 56 years received induction chemotherapy commencing with high-dose cytosine arabinoside (Ara-C) and etoposide (Protocol BF11), followed by Ara-C, 6 thioguanine (6TG). A total of 67% of patients entered remission using these drugs. An anthracycline was added for those patients not in remission. The overall remission rate (CR) was 86.5% (45/52), with a minimum follow-up of 90 days. Patients are hospitalised for relatively short periods, and consequently require less blood product and antibiotic support. Patients in continuing first remission following induction with Ara-C and etoposide are similar in number to those in continuing first remission who initially received an anthracycline. This would imply that the efficiency of Ara-C and etoposide in inducing long-term disease-term survival is comparable with anthracycline-containing regimens. We conclude that high-dose Ara-C and etoposide used in the first induction cycle for treating AML have good antileukaemic effect with acceptable toxicity. Nature Publishing Group 1990-11 /pmc/articles/PMC1971542/ /pubmed/2245176 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Parikh, P. Powles, R. Treleaven, J. Helenglass, G. Gore, M. Rose, M. Talbot, D. Milan, S. Smith, C. Pinkerton, R. High-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study. |
title | High-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study. |
title_full | High-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study. |
title_fullStr | High-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study. |
title_full_unstemmed | High-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study. |
title_short | High-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study. |
title_sort | high-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971542/ https://www.ncbi.nlm.nih.gov/pubmed/2245176 |
work_keys_str_mv | AT parikhp highdosecytosinearabinosideplusetoposideasinitialtreatmentforacutemyeloidleukaemiaasinglecentrestudy AT powlesr highdosecytosinearabinosideplusetoposideasinitialtreatmentforacutemyeloidleukaemiaasinglecentrestudy AT treleavenj highdosecytosinearabinosideplusetoposideasinitialtreatmentforacutemyeloidleukaemiaasinglecentrestudy AT helenglassg highdosecytosinearabinosideplusetoposideasinitialtreatmentforacutemyeloidleukaemiaasinglecentrestudy AT gorem highdosecytosinearabinosideplusetoposideasinitialtreatmentforacutemyeloidleukaemiaasinglecentrestudy AT rosem highdosecytosinearabinosideplusetoposideasinitialtreatmentforacutemyeloidleukaemiaasinglecentrestudy AT talbotd highdosecytosinearabinosideplusetoposideasinitialtreatmentforacutemyeloidleukaemiaasinglecentrestudy AT milans highdosecytosinearabinosideplusetoposideasinitialtreatmentforacutemyeloidleukaemiaasinglecentrestudy AT smithc highdosecytosinearabinosideplusetoposideasinitialtreatmentforacutemyeloidleukaemiaasinglecentrestudy AT pinkertonr highdosecytosinearabinosideplusetoposideasinitialtreatmentforacutemyeloidleukaemiaasinglecentrestudy |