全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
ISRN Oncology  2013 

Clinical Stages in Patients with Primary and Subsequent Cancers Based on the Czech Cancer Registry 1976–2005

DOI: 10.1155/2013/829486

Full-Text   Cite this paper   Add to My Lib

Abstract:

Of 1,486,984 new cancers registered in the Czech Cancer Registry in 1976-2005, 290,312 (19.5%) were multiple malignant neoplasms (MMNs), of which there were 65,292 primary and 89,796 subsequent cases in men and 59,970 primary and 75,254 subsequent cases in women. The duplicities were higher in women, and the triplicities and others (3–6 MMNs) were higher in men. The most frequent diagnoses were the primary cancers of skin, gastrointestinal and urinary tract, male genital organs, respiratory tract in men, and cancers of skin, breast, female genital organs, and gastrointestinal tract in women. The analysis of the early and advanced clinical stages shows that the number of subsequent advanced stages increased after primary advanced stages. Their time-age-space distributions visualized maps of MMNs in 14 Czech regions. These results support the improvement of algorithms of dispensary care for the early detection of the subsequent neoplasms. 1. Introduction The health status of the Czech population can be seen as very vulnerable, mainly because of the high risk of cancer especially in younger age. This fact is confirmed by data in Globocan 2008 [1]. Cancer diagnoses are registered since 1959. The IARC criteria are used were for their notificationed since May 1976 by criteria of the IARC. The annual surveys of Health Information and Statistics of the Czech Republic [2] confirmed the continued trend of cancer occurrence, observed in the Czech areas from 1905 [3] and continuously described from 1933 [4]. The cancer incidence increased from 24,471 (254.4/100,000) in 1959 over 35,407 (347.5/100,000) in 1977 to 78,846 (751.5/100,000) in 2009 [2]. In view of new diagnostic and treatment modalities, the prevalence of cancers (ICD-10: C00-97, D00-09) increased from 174,311 (1,682.2/100,000) in 1989 to 461,545 (4,510/100,000) in 2005. Under the conditions of continuous diagnostics, treatment, medical surveillance, and cancer evidence, the survivors can reach in 2015 nearly 317,000 cases in men (of which 33.2% in age 35–64 years) and 434,000 in women (of which 42.6% in age 35–64 years) [5]. The differences between the numbers of cases and numbers of persons indicated the multiple malignant neoplasms (MMNs). After the preliminary report of their trend [6], this paper is another contribution to this issue. 2. Methods The data of MMNs were based on the number of cancers reported to the Czech Cancer Registry between May 1976 and December 2005 and were verified and anonymised up to October 17, 2007. The percentage of multiple cancers of all diagnoses (ICD-10: C00-97,

References

[1]  IARC, “Globocan,” Lyon, France, IARC, 2008, http://globocan.iarc.fr/.
[2]  IHIS, Cancer incidence in the Czech Republic. Health statistics, editorial series, http://www.uzis.com/.
[3]  “Twenty-five years of the Czech Association for combat and exploration of malignant tumors in Prague,” Prague, Czech Republic, 1930.
[4]  J. Weiss, “Contribution to the statistics of the cancer increasing,” Practical Medicine, vol. 22, article 617, 1933.
[5]  M. Kone?ny, E. Geryk, P. Kubí?ek, et al., Cancer Prevalence in the Czech Republic, 1989-2005-2015, vol. 69, Masaryk University, Brno, Czech Republic, 2008.
[6]  E. Geryk, P. Dítě, J. Kozel, et al., “Cancer multiplicites in the Czech population,” Casopís Léka?? ?eskych, vol. 149, no. 4, pp. 178–183, 2010 (Czech).
[7]  E. Geryk, M. Bendová, and J. Kozel, “Breast cancer and subsequent primary malignant neoplasms in the Czech Republic 1976–2005,” Oncology, vol. 3, no. 1, pp. 54–61, 2009 (Czech).
[8]  E. Geryk, P. Dítě, L. Sedláková, et al., “Trends of multiple non-melanoma skin cancers in a view of their epidemiology,” Practice Dermatology, vol. 4, no. 1, pp. 5–9, 2010 (Czech).
[9]  E. Geryk, P. Dítě, J. Kozel, et al., “Other primary neoplasms in patients with prostate cancer in comparison of its incidence, mortality and prevalence,” Oncology, vol. 4, no. 2, pp. 89–93, 2010 (Czech).
[10]  P. Dítě and E. Geryk, “Trends of primary and subsequent cancers of the gastrointestinal tract in the czech population, 1976–2005,” Digestive Diseases, vol. 28, no. 4-5, pp. 657–669, 2010.
[11]  E. Geryk, J. Kozel, R. ?tampach et al., “Multiple cancers of nervous system and other primary neoplasms,” Oncology, vol. 5, no. 3, pp. 175–180, 2011 (Czech).
[12]  T. Horvath, E. Geryk, J. Kozel, et al., “Lung cancer in multiple malignant neoplasms,” in Proceedings of the 3rd Lung Cancer Conference, Geneva, Switzerland, 2012.
[13]  E. Geryk, J. Kozel, T. Horváth, et al., “Patients with multiple cancers of head and neck,” Oncology, vol. 6, no. 5, pp. 260–265, 2012 (Czech).
[14]  E. Geryk, J. Kozel, D. Pacík, R. ?tampach, and T. Horváth, “Multiple cancers of testis,” Practice Urology, vol. 14, no. 1, pp. 34–38, 2013 (Czech).
[15]  E. Geryk, D. Pacik, J. Kozel, et al., “Penile cancers associated with occurrence of other neoplasms,” Urology Letters, vol. 10, no. 4, pp. 1–6, 2012 (Czech).
[16]  E. Geryk, P. Ko?ka, P. Dítě, et al., “Cancers, health and economy: parts of Pandoras box?” Oncology, vol. 7, no. 1, pp. 314–320, 2013 (Czech).
[17]  R. E. Curtis, D. M. Freedman, E. Ron, et al., New Malignancies Among Cancer Survivors: SEER Cancer Registries 1973–2000, National Cancer Institute, Bethesda, Md, USA, 2006.
[18]  ACS, “Multiple primary cancers,” in Cancer Facts and Figures 2009, pp. 24–41, American Cancer Society, Atlanta, Ga, USA, 2009.
[19]  T. Billroth and A. von Winiwarer, Die Allgemeine Chirurgische Patologie Und Therapie, G. Reimer, Berlin, Germany, 1889.
[20]  J. M. Holland, A. Arsanjani, B. J. Liem, S. Christopher Hoffelt, J. I. Cohen, and K. R. Stevens, “Second malignancies in early stage laryngeal carcinoma patients treated with radiotherapy,” Journal of Laryngology and Otology, vol. 116, no. 3, pp. 190–193, 2002.
[21]  N. N. Baxter, J. E. Tepper, S. B. Durham, D. A. Rothenberger, and B. A. Virnig, “Increased risk of rectal cancer after prostate radiation: a population-based study,” Gastroenterology, vol. 128, no. 4, pp. 819–824, 2005.
[22]  M. Clarke, R. Collins, S. Darby, et al., “Effects of radiotherapy and of differences in the extent of surgery for early breast cancer on local recurrence and 15-year survival: an overview of the randomised trials,” The Lancet, vol. 366, no. 9503, pp. 2087–2106, 2005.
[23]  C. Rubino, A. Shamsaldin, M. G. Lê et al., “Radiation dose and risk of soft tissue and bone sarcoma after breast cancer treatment,” Breast Cancer Research and Treatment, vol. 89, no. 3, pp. 277–288, 2005.
[24]  P. Valagussa, A. Moliterni, M. Terenziani, M. Zambetti, and G. Bonadonna, “Second malignancies following CMF-based adjuvant chemotherapy in resectable breast cancer,” Annals of Oncology, vol. 5, no. 9, pp. 803–808, 1994.
[25]  J. M. Kaldor, N. E. Day, B. Kittelmann et al., “Bladder tumours following chemotherapy and radiotherapy for ovarian cancer: a case-control study,” International Journal of Cancer, vol. 63, no. 1, pp. 1–6, 1995.
[26]  L. B. Travis, M. Gospodarowicz, R. E. Curtis, et al., “Lung cancer following chemotherapy and radiotherapy for Hodgkin's disease,” Journal of the National Cancer Institute, vol. 94, no. 3, pp. 182–192, 2002.
[27]  R. E. Curtis, D. M. Freedman, M. E. Sherman, and J. F. Fraumeni Jr., “Risk of malignant mixed mullerian tumors after tamoxifen therapy for breast cancer,” Journal of the National Cancer Institute, vol. 96, no. 1, pp. 70–74, 2004.
[28]  A. J. Swerdlow, M. E. Jones, D. H. Brewster et al., “Tamoxifen treatment for breast cancer and risk of endometrial cancer: a case-control study,” Journal of the National Cancer Institute, vol. 97, no. 5, pp. 375–384, 2005.
[29]  C. K. Fairley, A. G. R. Sheil, J. J. McNeil et al., “The risk of ano-genital malignancies in dialysis and transplant patients,” Clinical Nephrology, vol. 41, no. 2, pp. 101–105, 1994.
[30]  S. A. Birkeland, H. H. Storm, L. U. Lamm et al., “Cancer risk after renal transplantation in the nordic countries, 1964–1986,” International Journal of Cancer, vol. 60, no. 2, pp. 183–189, 1995.
[31]  R. E. Curtis, P. A. Rowlings, H. J. Deeg et al., “Solid cancers after bone marrow transplantation,” The New England Journal of Medicine, vol. 336, no. 13, pp. 897–904, 1997.
[32]  S. Euvrard, J. Kanitakis, and A. Claudy, “Skin cancers after organ transplantation,” The New England Journal of Medicine, vol. 348, no. 17, pp. 1681–1691, 2003.
[33]  T. Kirchhoff, N. D. Kauff, N. Mitra et al., “BRCA mutations and risk of prostate cancer in Ashkenazi jews,” Clinical Cancer Research, vol. 10, no. 9, pp. 2918–2921, 2004.
[34]  H. D. Nelson, L. H. Huffman, R. Fu, and E. L. Harris, “Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: systematic evidence review for the U.S. Preventive Services Task Force,” Annals of Internal Medicine, vol. 143, no. 5, pp. 326–379, 2005.
[35]  R. S. Ostfeld, G. E. Glass, and F. Keesing, “Spatial epidemiology: an emerging (or re-emerging) discipline,” Trends in Ecology and Evolution, vol. 20, no. 6, pp. 328–336, 2005.
[36]  M. Kone?ny and W. Reinhardt, “Early warning and disaster management: the importance of geographic information,” International Journal of Digital Earth, vol. 3, no. 3, pp. 217–220, 2010.
[37]  R. ?tampach, K. Kone?ny, et al., “Dynamic cartographic methods for visualization of health statistics,” in Cartography in Central and Eastern Europe, pp. 431–442, Springer, Berlin, Germany, 2010.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133