
Opinion|Videos|May 8, 2025
Utilizing the RSClin Tool to Inform Breast Cancer Treatment Decisions in the Practice Setting
Panelists discuss how the RSClin tool provides more personalized information by combining recurrence scores with clinicopathological data, offering patients specific predictions about their prognosis and potential chemotherapy benefit rather than general outcomes for patients with similar scores.
Advertisement
Tools for Result Interpretation
Main Discussion Topics:
- Use of the RSClin tool to individualize risk assessment beyond recurrence score alone
- Integration of clinical-pathological features with genomic information
- Communication approaches with patients about risk and benefit
Key Points for Physicians:
- The RSClin tool combines recurrence score with clinical-pathological data for more precise estimates of recurrence risk and chemotherapy benefit.
- The tool offers multiple visualization options to facilitate patient understanding.
- Physicians should adapt their communication approach based on patient information needs.
Notable Insights:
- Patients often want to know their individual prognosis rather than population-based outcomes.
- Some patients prefer detailed statistical information whereas others simply want clinician recommendations.
Clinical Significance: Tools such as RSClin enhance the clinical utility of genomic testing by providing more individualized risk estimates that can be communicated to patients in ways that match their information preferences.
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

