At this time staging and prognostication of Chronic lymphocytic leukemia( CLL) is performed by 2 equivalent clinical staging systems developed 30 to 35 years ago by Binet and Rai Both systems use low-cost, simple components such as blood counts and physical examination to identify 3 major prognostic subgroups. Despite these advantages, the clinical staging systems do not reflect the high unpredictability of CLL, nor do they account for known biological characteristics of CLL cells predicting survival and response to therapy. That was the motivation for Mayo Clinic, and Wierda proposed to combine a set of clinical risk factors, to develop a prognostic index (PI) stratifying patients in three risk groups with different expected median survival, and a nomogram, estimating individual patient survivals. Here we report the results from a study designed to evaluate Wierda`s nomogram and prognostic index on Macedonian CLL population. Material and methods: We analyzed medical data of 300 CLL patients diagnosed and treated at University Clinic of Hematology -Skopje Macedonia from a period of 10 years. We used Wierda`s prognostics index and a nomogram, to see 5- and 10-year survival probability and estimated median survival time. Results: There were 300 CLL patients who had traditional and biological prognostic factors evaluated. According to prognostic index a classification tree was built that identified three subsets of patients. Estimated median survival at low risk subset of patients with prognostic nomogram <80 was 68, 7 months, and 37, 5 months respectively at high risk subsets of patients with prognostic nomogram >80. Projected survival in respectively low, intermediate and high-risk groups was 91, 7%, 80%, 50%, and 81, 5%, 60%, 10% at 5-year and10-year, respectively. Conclusion: We use this model to identify patients at high risk for progression to treatment and we are experiencing a paradigm shift toward personalized medicine. This prognostic model may help patients and clinicians in clinical decision making as well as in clinical research and clinical trial design.
Published in | Science Journal of Clinical Medicine (Volume 3, Issue 6) |
DOI | 10.11648/j.sjcm.20140306.15 |
Page(s) | 124-128 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2014. Published by Science Publishing Group |
CLL, Prognostic Index, Nomogram, Prognosis
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APA Style
Trajkova Sanja, Cevreska Lidija, Ivanovski Martin, Dukovski Dusko, Simjanovska-Popova Marija, et al. (2014). Evaluation of Reproducibility of Prognostic Index and Nomogram in Prognosis, and Therapeutically Approach of Patients with Chronic Lymphocytic Leukaemia-Single Centre Experience. Science Journal of Clinical Medicine, 3(6), 124-128. https://doi.org/10.11648/j.sjcm.20140306.15
ACS Style
Trajkova Sanja; Cevreska Lidija; Ivanovski Martin; Dukovski Dusko; Simjanovska-Popova Marija, et al. Evaluation of Reproducibility of Prognostic Index and Nomogram in Prognosis, and Therapeutically Approach of Patients with Chronic Lymphocytic Leukaemia-Single Centre Experience. Sci. J. Clin. Med. 2014, 3(6), 124-128. doi: 10.11648/j.sjcm.20140306.15
AMA Style
Trajkova Sanja, Cevreska Lidija, Ivanovski Martin, Dukovski Dusko, Simjanovska-Popova Marija, et al. Evaluation of Reproducibility of Prognostic Index and Nomogram in Prognosis, and Therapeutically Approach of Patients with Chronic Lymphocytic Leukaemia-Single Centre Experience. Sci J Clin Med. 2014;3(6):124-128. doi: 10.11648/j.sjcm.20140306.15
@article{10.11648/j.sjcm.20140306.15, author = {Trajkova Sanja and Cevreska Lidija and Ivanovski Martin and Dukovski Dusko and Simjanovska-Popova Marija and Stankovik Svetlana and Panovska-Stavridis Irina}, title = {Evaluation of Reproducibility of Prognostic Index and Nomogram in Prognosis, and Therapeutically Approach of Patients with Chronic Lymphocytic Leukaemia-Single Centre Experience}, journal = {Science Journal of Clinical Medicine}, volume = {3}, number = {6}, pages = {124-128}, doi = {10.11648/j.sjcm.20140306.15}, url = {https://doi.org/10.11648/j.sjcm.20140306.15}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.sjcm.20140306.15}, abstract = {At this time staging and prognostication of Chronic lymphocytic leukemia( CLL) is performed by 2 equivalent clinical staging systems developed 30 to 35 years ago by Binet and Rai Both systems use low-cost, simple components such as blood counts and physical examination to identify 3 major prognostic subgroups. Despite these advantages, the clinical staging systems do not reflect the high unpredictability of CLL, nor do they account for known biological characteristics of CLL cells predicting survival and response to therapy. That was the motivation for Mayo Clinic, and Wierda proposed to combine a set of clinical risk factors, to develop a prognostic index (PI) stratifying patients in three risk groups with different expected median survival, and a nomogram, estimating individual patient survivals. Here we report the results from a study designed to evaluate Wierda`s nomogram and prognostic index on Macedonian CLL population. Material and methods: We analyzed medical data of 300 CLL patients diagnosed and treated at University Clinic of Hematology -Skopje Macedonia from a period of 10 years. We used Wierda`s prognostics index and a nomogram, to see 5- and 10-year survival probability and estimated median survival time. Results: There were 300 CLL patients who had traditional and biological prognostic factors evaluated. According to prognostic index a classification tree was built that identified three subsets of patients. Estimated median survival at low risk subset of patients with prognostic nomogram 80. Projected survival in respectively low, intermediate and high-risk groups was 91, 7%, 80%, 50%, and 81, 5%, 60%, 10% at 5-year and10-year, respectively. Conclusion: We use this model to identify patients at high risk for progression to treatment and we are experiencing a paradigm shift toward personalized medicine. This prognostic model may help patients and clinicians in clinical decision making as well as in clinical research and clinical trial design.}, year = {2014} }
TY - JOUR T1 - Evaluation of Reproducibility of Prognostic Index and Nomogram in Prognosis, and Therapeutically Approach of Patients with Chronic Lymphocytic Leukaemia-Single Centre Experience AU - Trajkova Sanja AU - Cevreska Lidija AU - Ivanovski Martin AU - Dukovski Dusko AU - Simjanovska-Popova Marija AU - Stankovik Svetlana AU - Panovska-Stavridis Irina Y1 - 2014/11/27 PY - 2014 N1 - https://doi.org/10.11648/j.sjcm.20140306.15 DO - 10.11648/j.sjcm.20140306.15 T2 - Science Journal of Clinical Medicine JF - Science Journal of Clinical Medicine JO - Science Journal of Clinical Medicine SP - 124 EP - 128 PB - Science Publishing Group SN - 2327-2732 UR - https://doi.org/10.11648/j.sjcm.20140306.15 AB - At this time staging and prognostication of Chronic lymphocytic leukemia( CLL) is performed by 2 equivalent clinical staging systems developed 30 to 35 years ago by Binet and Rai Both systems use low-cost, simple components such as blood counts and physical examination to identify 3 major prognostic subgroups. Despite these advantages, the clinical staging systems do not reflect the high unpredictability of CLL, nor do they account for known biological characteristics of CLL cells predicting survival and response to therapy. That was the motivation for Mayo Clinic, and Wierda proposed to combine a set of clinical risk factors, to develop a prognostic index (PI) stratifying patients in three risk groups with different expected median survival, and a nomogram, estimating individual patient survivals. Here we report the results from a study designed to evaluate Wierda`s nomogram and prognostic index on Macedonian CLL population. Material and methods: We analyzed medical data of 300 CLL patients diagnosed and treated at University Clinic of Hematology -Skopje Macedonia from a period of 10 years. We used Wierda`s prognostics index and a nomogram, to see 5- and 10-year survival probability and estimated median survival time. Results: There were 300 CLL patients who had traditional and biological prognostic factors evaluated. According to prognostic index a classification tree was built that identified three subsets of patients. Estimated median survival at low risk subset of patients with prognostic nomogram 80. Projected survival in respectively low, intermediate and high-risk groups was 91, 7%, 80%, 50%, and 81, 5%, 60%, 10% at 5-year and10-year, respectively. Conclusion: We use this model to identify patients at high risk for progression to treatment and we are experiencing a paradigm shift toward personalized medicine. This prognostic model may help patients and clinicians in clinical decision making as well as in clinical research and clinical trial design. VL - 3 IS - 6 ER -