Deep myelosuppression, an officially sanctioned effect of non-selective cytotoxic cancer therapy, would be expected to be incompatible with mounting of a powerful host defense against spontaneous malignancy. To explore this theoretical difficulty, we used middle age as a natural model of a temporary decline in lymphocytopoiesis, caused by physiological thymus involution. The impact of middle age on the levels of death from nonmalignant and malignant diseases was analyzed retrospectively, using population health data from Europe (the European Network of Economic Policy Research Institutes, 1995); the UK (Statistics Team at the Cancer Research UK, and the Office for National Statistics cancer survival rates for 2007-2010), and the USA (National Center for Health Statistics, 1987-2007; National Vital Statistics System, 1999-2010; National Cancer Institute's Surveillance, Epidemiology, and End Results [SEER], 1992-2010). The rate of death and survival used to check whether the vectors of middle age-specific changes of these parameters are opposite or coincident in cancer patients and those with certain non-malignant somatic diseases. According the temporary trend on a middle- age portion of plot, the curves were graded negative or positive (+ = viability is not change or goes up; - = viability goes down).Comparisons of aggregate data showed that middle age exerted opposite effects on the health of those with cancer and non-malignant diseases. In middle age, serious health conditions, such as some cancers, are easier to treat, but the overall quality of life is reduced by various morbidities, especially infections. The comparing of the impact of middle age on the viability of patients with nonmalignant and malignant diseases in alternative terms of immunity or morphogenesis leads to recognition of trophic contribution of thymus into tumor development. By analogy, we assume that use of cytotoxic therapy can exert indirect benefit, thus compromising hemato- lymphocytopoiesis.
Published in | Cancer Research Journal (Volume 2, Issue 6) |
DOI | 10.11648/j.crj.20140206.14 |
Page(s) | 114-120 |
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 |
Death Rates, Malignancy, Middle Age, Mielopoiesis, Populations
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APA Style
Alexei N. Shoutko, Lyudmila P. Ekimova. (2014). The Impact of Middle Age on the Viability of Patients with Nonmalignant and Malignant Diseases. Cancer Research Journal, 2(6), 114-120. https://doi.org/10.11648/j.crj.20140206.14
ACS Style
Alexei N. Shoutko; Lyudmila P. Ekimova. The Impact of Middle Age on the Viability of Patients with Nonmalignant and Malignant Diseases. Cancer Res. J. 2014, 2(6), 114-120. doi: 10.11648/j.crj.20140206.14
AMA Style
Alexei N. Shoutko, Lyudmila P. Ekimova. The Impact of Middle Age on the Viability of Patients with Nonmalignant and Malignant Diseases. Cancer Res J. 2014;2(6):114-120. doi: 10.11648/j.crj.20140206.14
@article{10.11648/j.crj.20140206.14, author = {Alexei N. Shoutko and Lyudmila P. Ekimova}, title = {The Impact of Middle Age on the Viability of Patients with Nonmalignant and Malignant Diseases}, journal = {Cancer Research Journal}, volume = {2}, number = {6}, pages = {114-120}, doi = {10.11648/j.crj.20140206.14}, url = {https://doi.org/10.11648/j.crj.20140206.14}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.crj.20140206.14}, abstract = {Deep myelosuppression, an officially sanctioned effect of non-selective cytotoxic cancer therapy, would be expected to be incompatible with mounting of a powerful host defense against spontaneous malignancy. To explore this theoretical difficulty, we used middle age as a natural model of a temporary decline in lymphocytopoiesis, caused by physiological thymus involution. The impact of middle age on the levels of death from nonmalignant and malignant diseases was analyzed retrospectively, using population health data from Europe (the European Network of Economic Policy Research Institutes, 1995); the UK (Statistics Team at the Cancer Research UK, and the Office for National Statistics cancer survival rates for 2007-2010), and the USA (National Center for Health Statistics, 1987-2007; National Vital Statistics System, 1999-2010; National Cancer Institute's Surveillance, Epidemiology, and End Results [SEER], 1992-2010). The rate of death and survival used to check whether the vectors of middle age-specific changes of these parameters are opposite or coincident in cancer patients and those with certain non-malignant somatic diseases. According the temporary trend on a middle- age portion of plot, the curves were graded negative or positive (+ = viability is not change or goes up; - = viability goes down).Comparisons of aggregate data showed that middle age exerted opposite effects on the health of those with cancer and non-malignant diseases. In middle age, serious health conditions, such as some cancers, are easier to treat, but the overall quality of life is reduced by various morbidities, especially infections. The comparing of the impact of middle age on the viability of patients with nonmalignant and malignant diseases in alternative terms of immunity or morphogenesis leads to recognition of trophic contribution of thymus into tumor development. By analogy, we assume that use of cytotoxic therapy can exert indirect benefit, thus compromising hemato- lymphocytopoiesis.}, year = {2014} }
TY - JOUR T1 - The Impact of Middle Age on the Viability of Patients with Nonmalignant and Malignant Diseases AU - Alexei N. Shoutko AU - Lyudmila P. Ekimova Y1 - 2014/12/02 PY - 2014 N1 - https://doi.org/10.11648/j.crj.20140206.14 DO - 10.11648/j.crj.20140206.14 T2 - Cancer Research Journal JF - Cancer Research Journal JO - Cancer Research Journal SP - 114 EP - 120 PB - Science Publishing Group SN - 2330-8214 UR - https://doi.org/10.11648/j.crj.20140206.14 AB - Deep myelosuppression, an officially sanctioned effect of non-selective cytotoxic cancer therapy, would be expected to be incompatible with mounting of a powerful host defense against spontaneous malignancy. To explore this theoretical difficulty, we used middle age as a natural model of a temporary decline in lymphocytopoiesis, caused by physiological thymus involution. The impact of middle age on the levels of death from nonmalignant and malignant diseases was analyzed retrospectively, using population health data from Europe (the European Network of Economic Policy Research Institutes, 1995); the UK (Statistics Team at the Cancer Research UK, and the Office for National Statistics cancer survival rates for 2007-2010), and the USA (National Center for Health Statistics, 1987-2007; National Vital Statistics System, 1999-2010; National Cancer Institute's Surveillance, Epidemiology, and End Results [SEER], 1992-2010). The rate of death and survival used to check whether the vectors of middle age-specific changes of these parameters are opposite or coincident in cancer patients and those with certain non-malignant somatic diseases. According the temporary trend on a middle- age portion of plot, the curves were graded negative or positive (+ = viability is not change or goes up; - = viability goes down).Comparisons of aggregate data showed that middle age exerted opposite effects on the health of those with cancer and non-malignant diseases. In middle age, serious health conditions, such as some cancers, are easier to treat, but the overall quality of life is reduced by various morbidities, especially infections. The comparing of the impact of middle age on the viability of patients with nonmalignant and malignant diseases in alternative terms of immunity or morphogenesis leads to recognition of trophic contribution of thymus into tumor development. By analogy, we assume that use of cytotoxic therapy can exert indirect benefit, thus compromising hemato- lymphocytopoiesis. VL - 2 IS - 6 ER -