By Pierce D. A.
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Extra resources for Age-time patterns of cancer to be anticipated from exposure to general mutagens
This prediction can suggest follow-up strategies focusing on the symptoms of the possible – or, better, of the most probable – subsequent primary tumors so as to allow for early-warning approaches to the future malignancy. Moreover, also an estimate of when the next neoplasm will show itself is of interest. Roughly speaking, the time between the two diseases turns out to be a stochastic variable with an exponential or geometric distribution; this result is not surprising and is confirmed by the current literature.
3%. 3 Bioinformatics in MPM: Using Decision Trees To Predict a Second Tumor Site 43 Fig. 7 Frequency tree for Hodgkin lymphoma. 09* 44 A. Cavallo, C. Dodaro Urinary Bladder No sub-districts are defined with the urinary bladder as primary site. 8 shows the prediction tree. 21 per 10,000. The risk increases for cancers of the urinary, respiratory, and male genital systems and decreases for skin cancers, excluding basal and squamous carcinomas, and for Kaposi sarcoma. 10. In this case, the large SIR for cancers of the female respiratory system is responsible for the high frequency of cancers of the lung and bronchus for women, while for men the high underlying frequency of prostate cancer, although associated with a relatively moderate increase in risk of 15%, makes prostate cancer the second tumor in about one third of the cases considered.
Histologic type, with different coding criteria applied over the years, harmonized according to  and the SEER documentation 4. Stage A, to be used cautiously, as reported in , with values: in situ (noninvasive neoplams), localized (confined to the organ of origin), regional (extended into surrounding organs), distant (extended to remote organs), 3 Bioinformatics in MPM: Using Decision Trees To Predict a Second Tumor Site 29 localized/regional (only prostate), unstaged (insufficient information).
Age-time patterns of cancer to be anticipated from exposure to general mutagens by Pierce D. A.