2012
DOI: 10.1182/blood-2011-10-383380
|View full text |Cite
|
Sign up to set email alerts
|

FGFR2 genotype and risk of radiation-associated breast cancer in Hodgkin lymphoma

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
27
1

Year Published

2012
2012
2020
2020

Publication Types

Select...
5
3

Relationship

0
8

Authors

Journals

citations
Cited by 29 publications
(28 citation statements)
references
References 23 publications
0
27
1
Order By: Relevance
“…[6][7][8] Best et al showed 2 variants at chromosome 6q21 to be associated with subsequent malignant neoplasm in survivors of HL treated with radiation therapy as children but not as adults. 6 Ma et al showed that genetic variation in FGFR2 influences breast cancer risk in HL patients treated with radiotherapy.…”
Section: Second Malignancymentioning
confidence: 99%
See 2 more Smart Citations
“…[6][7][8] Best et al showed 2 variants at chromosome 6q21 to be associated with subsequent malignant neoplasm in survivors of HL treated with radiation therapy as children but not as adults. 6 Ma et al showed that genetic variation in FGFR2 influences breast cancer risk in HL patients treated with radiotherapy.…”
Section: Second Malignancymentioning
confidence: 99%
“…Further work on genetic susceptibility to developing late effects of treatment can help to guide initial treatment decision and allow targeted and tailored followup of survivors. 6,8 Additional research efforts on correlating radiation dosimetric parameters of specific organs with late effects would improve our understanding of the relationship between radiation dosevolume and long-term risks and guide future radiation treatment planning. 24,34 There are emerging data on an association between anthracyclines and, not just cardiac risk, but also solid tumors, and further follow-up is needed to confirm the findings.…”
Section: Future Directionsmentioning
confidence: 99%
See 1 more Smart Citation
“…1 These studies have a small number of patients that developed second malignancies, 49 and 59 patients, respectively. Underlying explanation for our findings, that a prior malignancy increases the risk of second malignancies in MM patients, could include genetic susceptibilities, [17][18][19][20][21][22][32][33][34][35] immunosuppression, [36][37][38] and therapy-related cancers. 12,13,39 We found MM patients with a prior cancer diagnosis to have an increased risk of developing hematological malignancy, melanoma, nonmelanoma skin cancer, and respiratory malignancy compared with MM patients who did not.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, less pathogenic low-penetrance genetic susceptibility might be more important. Recent studies identified allelic variants in PRDM1 and FGFR2 to predispose Hodgkin lymphoma survivors to radiationinduced breast cancer (Best et al 2011, Ma et al 2012). …”
Section: Epidemiology and Host-related Risk Factorsmentioning
confidence: 99%