Related Experiment Video
Updated: Sep 20, 2025

10:33
Expedited Radiation Biodosimetry by Automated Dicentric Chromosome Identification ADCI and Dose Estimation
Published on: September 4, 2017
15.9K
DCIS: Risk Assessment in the Molecular Era
Christin A Knowlton1, Rachel B Jimenez2, Meena S Moran1
1Department of Therapeutic Radiology, Yale School of Medicine; New Haven, CT.
Seminars in Radiation Oncology
|June 10, 2022
Summary
Ductal carcinoma in situ (DCIS) treatment is evolving. New genomic assays help personalize decisions about radiotherapy after breast-conserving surgery, potentially de-escalating care for low-risk patients.
Area of Science:
- Oncology
- Genomics
- Breast Cancer Research
Background:
- Ductal carcinoma in situ (DCIS) accounts for 20% of breast cancers.
- Standard treatment involves breast-conserving surgery (BCS) and radiotherapy (RT), with endocrine therapy for hormone-receptor positive disease.
- RT significantly reduces in-breast recurrence but prompts interest in de-escalation for low-risk cases.
Purpose of the Study:
- To review current molecular risk assessment tools for DCIS.
- To evaluate their role in guiding postoperative RT decisions after BCS.
- To discuss ongoing trials on omitting surgery for low-risk DCIS.
Main Methods:
- Review of published literature on DCIS molecular assays.
- Analysis of clinical-pathologic features used in risk stratification.
- Discussion of genomic assays like Oncotype DX Breast DCIS Score and DCISionRT.
- Examination of clinical trials investigating treatment de-escalation.
Main Results:
- Genomic assays offer individualized prediction of RT benefit.
- These tools, combined with clinical-pathologic factors, enhance risk assessment.
- High local control rates with current BCT support de-escalation efforts.
Conclusions:
- Molecular assays show promise in personalizing RT recommendations for DCIS.
- Selective de-escalation of RT is a key focus in DCIS management.
- Further research and trials are exploring treatment omission for select low-risk DCIS patients.
Related Concept Videos
Mutagenicity and Carcinogenicity
1.4K
Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...
1.4K
Cancer-Critical Genes II: Tumor Suppressor Genes
8.2K
Genes usually encode proteins necessary for the proper functioning of a healthy cell. Mutations can often cause changes to the gene expression pattern, thereby altering the phenotype.
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
8.2K

