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Immunotherapy for Acute Myelogenous Leukaemia
One hundred and seven untreated patients with acute myelogenous leukaemia (AML) were admitted to St Bartholomew's Hospital between 10 October 1970 and 31 January 1973. Before receiving drugs to induce remission they were allocated alternatively into 2 groups to decide their remission treatment—...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1973
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008928/ https://www.ncbi.nlm.nih.gov/pubmed/4271320 |
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author | Powles, R. L. Crowther, D. Bateman, C. J. T. Beard, M. E. J. McElwain, T. J. Russell, J. Lister, T. A. Whitehouse, J. M. A. Wrigley, P. F. M. Pike, M. Alexander, P. Fairley, G. Hamilton |
author_facet | Powles, R. L. Crowther, D. Bateman, C. J. T. Beard, M. E. J. McElwain, T. J. Russell, J. Lister, T. A. Whitehouse, J. M. A. Wrigley, P. F. M. Pike, M. Alexander, P. Fairley, G. Hamilton |
author_sort | Powles, R. L. |
collection | PubMed |
description | One hundred and seven untreated patients with acute myelogenous leukaemia (AML) were admitted to St Bartholomew's Hospital between 10 October 1970 and 31 January 1973. Before receiving drugs to induce remission they were allocated alternatively into 2 groups to decide their remission treatment—a group to receive chemotherapy alone and a group to receive the same chemotherapy with immunotherapy. The patients were then given induction chemotherapy and 45 of them attained complete remission. All patients in remission then received chemotherapy consisting of 5 days treatment every 28 days. Patients receiving immunotherapy were also given multiple weekly intradermal injections of irradiated stored AML cells and Glaxo B.C.G. using a Heaf gun. There were 19 patients in the group which received only chemotherapy during remission; 7 of these patients remain alive (median survival after attaining remission 303 days) and only 5 are still in their first remission (median remission length 188 days). Twenty-three patients were allocated to receive immunotherapy during remission in addition to chemotherapy and 16 remain alive (median 545 days) and 8 are in their first remission (median 312 days). The difference in survival of the two groups is significant with a P value of 0·003. |
format | Text |
id | pubmed-2008928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1973 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20089282009-09-10 Immunotherapy for Acute Myelogenous Leukaemia Powles, R. L. Crowther, D. Bateman, C. J. T. Beard, M. E. J. McElwain, T. J. Russell, J. Lister, T. A. Whitehouse, J. M. A. Wrigley, P. F. M. Pike, M. Alexander, P. Fairley, G. Hamilton Br J Cancer Articles One hundred and seven untreated patients with acute myelogenous leukaemia (AML) were admitted to St Bartholomew's Hospital between 10 October 1970 and 31 January 1973. Before receiving drugs to induce remission they were allocated alternatively into 2 groups to decide their remission treatment—a group to receive chemotherapy alone and a group to receive the same chemotherapy with immunotherapy. The patients were then given induction chemotherapy and 45 of them attained complete remission. All patients in remission then received chemotherapy consisting of 5 days treatment every 28 days. Patients receiving immunotherapy were also given multiple weekly intradermal injections of irradiated stored AML cells and Glaxo B.C.G. using a Heaf gun. There were 19 patients in the group which received only chemotherapy during remission; 7 of these patients remain alive (median survival after attaining remission 303 days) and only 5 are still in their first remission (median remission length 188 days). Twenty-three patients were allocated to receive immunotherapy during remission in addition to chemotherapy and 16 remain alive (median 545 days) and 8 are in their first remission (median 312 days). The difference in survival of the two groups is significant with a P value of 0·003. Nature Publishing Group 1973-11 /pmc/articles/PMC2008928/ /pubmed/4271320 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 | Articles Powles, R. L. Crowther, D. Bateman, C. J. T. Beard, M. E. J. McElwain, T. J. Russell, J. Lister, T. A. Whitehouse, J. M. A. Wrigley, P. F. M. Pike, M. Alexander, P. Fairley, G. Hamilton Immunotherapy for Acute Myelogenous Leukaemia |
title | Immunotherapy for Acute Myelogenous Leukaemia |
title_full | Immunotherapy for Acute Myelogenous Leukaemia |
title_fullStr | Immunotherapy for Acute Myelogenous Leukaemia |
title_full_unstemmed | Immunotherapy for Acute Myelogenous Leukaemia |
title_short | Immunotherapy for Acute Myelogenous Leukaemia |
title_sort | immunotherapy for acute myelogenous leukaemia |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008928/ https://www.ncbi.nlm.nih.gov/pubmed/4271320 |
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