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Profil diagnostique et évolutif du myélome multiple au Sénégal: étude monocentrique de 2005 à 2016
INTRODUCTION: Accessibility to innovative multiple myeloma therapies is limited in sub-Saharan Africa. This study aimed to describe the diagnostic and evolutionary features observed during treatment of our patients with myeloma. METHODS: We conducted a retrospective, descriptive, analytical study (2...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5660322/ https://www.ncbi.nlm.nih.gov/pubmed/29187931 http://dx.doi.org/10.11604/pamj.2017.27.262.13164 |
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author | Fall, Seynabou Dieng, Fatma Diouf, Coumba Djiba, Boundia Ndao, Awa Cheikh Ndiaye, Fatou Samba Diago |
author_facet | Fall, Seynabou Dieng, Fatma Diouf, Coumba Djiba, Boundia Ndao, Awa Cheikh Ndiaye, Fatou Samba Diago |
author_sort | Fall, Seynabou |
collection | PubMed |
description | INTRODUCTION: Accessibility to innovative multiple myeloma therapies is limited in sub-Saharan Africa. This study aimed to describe the diagnostic and evolutionary features observed during treatment of our patients with myeloma. METHODS: We conducted a retrospective, descriptive, analytical study (2005 - 2016) of patients with myeloma included in the study based on International Myeloma Working Group (IMWG) Criteria (2003,2014) at the Hopital Aristide Le Dantec (Senegal). RESULTS: We collected data from 136 medical records (69 men, 67 women) of patients with an average age of 59 years ± 10.1 years, who were less than 65 years of age in 69.1% of cases. Tell-tale signs included bone pain (96.3%), renal failure (36.8%), infection (23.5%), pathological fracture (17.6%), spinal cord compression (16.9%) and malignant hypercalcaemia (16.2%). Isotopic antiglobulin test showed that anti-IgG could be detected in 61.3% of cases and Kappa in 65% of cases. Patients were classified stage III (59.4%) and I-II (40.6%)of the index staging system. The median survival of patients under conventional traitement (Méphalan-Prédnisone: 67.6%, innovative: 5.9%) was 20 months (1-78 months). Survival rates are better in the absence of neurological and infectious complications and for patients with score I-II of the index Staging System. CONCLUSION: In our study, multiple myeloma was frequently diagnosed before age 65, at advanced stage of tumor mass. Early detection and access to adequate therapies could improve overall survival. |
format | Online Article Text |
id | pubmed-5660322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-56603222017-11-29 Profil diagnostique et évolutif du myélome multiple au Sénégal: étude monocentrique de 2005 à 2016 Fall, Seynabou Dieng, Fatma Diouf, Coumba Djiba, Boundia Ndao, Awa Cheikh Ndiaye, Fatou Samba Diago Pan Afr Med J Research INTRODUCTION: Accessibility to innovative multiple myeloma therapies is limited in sub-Saharan Africa. This study aimed to describe the diagnostic and evolutionary features observed during treatment of our patients with myeloma. METHODS: We conducted a retrospective, descriptive, analytical study (2005 - 2016) of patients with myeloma included in the study based on International Myeloma Working Group (IMWG) Criteria (2003,2014) at the Hopital Aristide Le Dantec (Senegal). RESULTS: We collected data from 136 medical records (69 men, 67 women) of patients with an average age of 59 years ± 10.1 years, who were less than 65 years of age in 69.1% of cases. Tell-tale signs included bone pain (96.3%), renal failure (36.8%), infection (23.5%), pathological fracture (17.6%), spinal cord compression (16.9%) and malignant hypercalcaemia (16.2%). Isotopic antiglobulin test showed that anti-IgG could be detected in 61.3% of cases and Kappa in 65% of cases. Patients were classified stage III (59.4%) and I-II (40.6%)of the index staging system. The median survival of patients under conventional traitement (Méphalan-Prédnisone: 67.6%, innovative: 5.9%) was 20 months (1-78 months). Survival rates are better in the absence of neurological and infectious complications and for patients with score I-II of the index Staging System. CONCLUSION: In our study, multiple myeloma was frequently diagnosed before age 65, at advanced stage of tumor mass. Early detection and access to adequate therapies could improve overall survival. The African Field Epidemiology Network 2017-08-08 /pmc/articles/PMC5660322/ /pubmed/29187931 http://dx.doi.org/10.11604/pamj.2017.27.262.13164 Text en © Seynabou Fall et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Fall, Seynabou Dieng, Fatma Diouf, Coumba Djiba, Boundia Ndao, Awa Cheikh Ndiaye, Fatou Samba Diago Profil diagnostique et évolutif du myélome multiple au Sénégal: étude monocentrique de 2005 à 2016 |
title | Profil diagnostique et évolutif du myélome multiple au Sénégal: étude monocentrique de 2005 à 2016 |
title_full | Profil diagnostique et évolutif du myélome multiple au Sénégal: étude monocentrique de 2005 à 2016 |
title_fullStr | Profil diagnostique et évolutif du myélome multiple au Sénégal: étude monocentrique de 2005 à 2016 |
title_full_unstemmed | Profil diagnostique et évolutif du myélome multiple au Sénégal: étude monocentrique de 2005 à 2016 |
title_short | Profil diagnostique et évolutif du myélome multiple au Sénégal: étude monocentrique de 2005 à 2016 |
title_sort | profil diagnostique et évolutif du myélome multiple au sénégal: étude monocentrique de 2005 à 2016 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5660322/ https://www.ncbi.nlm.nih.gov/pubmed/29187931 http://dx.doi.org/10.11604/pamj.2017.27.262.13164 |
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