2018
DOI: 10.1016/j.nurpra.2017.09.026
|View full text |Cite
|
Sign up to set email alerts
|

Second Primary Malignancies in Cancer Survivors

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
7
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(7 citation statements)
references
References 33 publications
0
7
0
Order By: Relevance
“…[7][8][9][10]12,13,[16][17][18][19][20][21][22][23] A number of factors, including (i) endogenous such as inherited/genetic predisposition (whether or not as part of specific syndromes) (Table 1 [24][25][26][27] ), abnormal embryo development, immune-associated diseases and/or comorbidities affecting carcinogen sensitivity; (ii) behavioral or lifestyle influences and environmental exposures; (iii) surveillance bias, or late iatrogenic effects of therapies for DTC/other primary tumors, could explain the enhanced general SPC risk and, particularly, in DTC patients. 3,4,15,18 Specifically, the association of radioactive iodine (RAI) therapy and risk of SPCs following DTC remains widely debated. 12 This association has suggested an enhanced SPC risk for both solid tumors and leukemia in patients with RAI-treated DTC compared with DTC survivors not exposed to RAI, mainly in younger patients.…”
Section: Current Situationmentioning
confidence: 99%
See 4 more Smart Citations
“…[7][8][9][10]12,13,[16][17][18][19][20][21][22][23] A number of factors, including (i) endogenous such as inherited/genetic predisposition (whether or not as part of specific syndromes) (Table 1 [24][25][26][27] ), abnormal embryo development, immune-associated diseases and/or comorbidities affecting carcinogen sensitivity; (ii) behavioral or lifestyle influences and environmental exposures; (iii) surveillance bias, or late iatrogenic effects of therapies for DTC/other primary tumors, could explain the enhanced general SPC risk and, particularly, in DTC patients. 3,4,15,18 Specifically, the association of radioactive iodine (RAI) therapy and risk of SPCs following DTC remains widely debated. 12 This association has suggested an enhanced SPC risk for both solid tumors and leukemia in patients with RAI-treated DTC compared with DTC survivors not exposed to RAI, mainly in younger patients.…”
Section: Current Situationmentioning
confidence: 99%
“…According to the National Cancer Institute's Surveillance, Epidemiology and End Results Program, cancers with the best survival rates are breast, Hodgkin's lymphoma, melanoma, prostate, testicular, and differentiated thyroid cancer (DCT), which all have a 5‐year survival rate of >85% (the 10‐year survival rate for papillary thyroid carcinoma [PTC] is 95–99%) 6 . Because of the high cure rates, most of these patients will survive having cancer, and will therefore be at increased risk for development of a second primary cancer (SPC), with a lifetime risk as high as 37% 4,5 …”
Section: Introduction and Historical Perspectivementioning
confidence: 99%
See 3 more Smart Citations