
Opinion|Videos|May 22, 2025
Key Takeaways and Future Directions: Genomic Assays in Breast Cancer Treatment
Panelists discuss how genomic assays have become essential tools in modern breast cancer treatment, preventing overtreatment by enabling customized treatment plans that determine not only whether patients need chemotherapy but also which specific agents they should receive and whether treatment should be given before or after surgery.
Advertisement
Clinical Case Scenarios and Concluding Remarks
Main Discussion Topics:
- Case scenario discussions for node-positive postmenopausal patients
- Approaches to large tumors in smaller breasts, with focus on breast conservation
- Synthesis of key takeaways about genomic testing utility
Key Points for Physicians:
- For a 64-year-old healthy patient with 1 positive lymph node and T1c tumor, a 21-gene assay would guide treatment decisions.
- For larger tumors in smaller breasts, genomic testing can help determine whether neoadjuvant chemotherapy or endocrine therapy would be more effective.
- Genomic assays have dramatically reduced unnecessary chemotherapy use while enabling tailored treatment approaches.
Notable Insights:
- Genomic testing results consistently outperform clinician predictions about tumor biology.
- For borderline breast conservation candidates, neoadjuvant endocrine therapy may be effective for select patients with favorable biology.
- Patient-specific factors including reconstruction timing, genetic testing results, and personal preferences influence the treatment decision process
Clinical Significance: Genomic testing has transformed breast cancer care by enabling personalized treatment decisions that balance efficacy and toxicity considerations, significantly reducing overtreatment while identifying patients who truly benefit from more aggressive approaches.
Advertisement
Related to this article

The FDA approved pirtobrutinib for untreated chronic lymphocytic leukemia, granted priority review to elinzanetant for breast cancer hot flashes, and more.

The 2026 amendment adds 40 new recommendations, including active surveillance, office-based treatment, and chemoablation for select recurrent low-grade disease.

The FDA has approved pirtobrutinib for the treatment of adult patients with previously untreated CLL or SLL harboring no known 17p deletion.

By finding a way to attack the most important human oncogene, KRAS, the UCSF chemical biologist launched a new era in cancer treatment.

TRE-515 earned fast track status in combination with KRAS inhibitors for G12C-mutated NSCLC after anti–PD-(L)1 therapy and platinum-based chemotherapy.

An NDA for zipalertinib in EGFR exon 20 insertion–positive NSCLC is being supported by phase 3 REZILIENT3 data.

Did you catch all of this week's top oncology news? Test your knowledge with OncLive's Weekly News Quiz.
Advertisement
Advertisement
Trending on OncLive
1
FDA Approves Pirtobrutinib for Previously Untreated CLL/SLL
2
FDA Grants Fast Track Designation to TRE-515 Plus KRAS Inhibitors in Pretreated KRAS G12C+ NSCLC
3
NDA Submission Is Initiated for Zipalertinib Plus Chemotherapy in Frontline EGFR Exon 20 Insertion+ NSCLC
4
Oral Azacitidine and Cedazuridine Meets Primary Pharmacokinetic End Point in MDS and CMML
5

