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The FDA has approved pertuzumab-dpzb (Poherdy) as a biosimilar to pertuzumab (Perjeta) in breast cancer, based on a review of various attributes, including safety and efficacy data.
FDA Approves Pertuzumab Biosimilar in Breast Cancer Indications

November 13th 2025

The FDA has approved pertuzumab-dpzb (Poherdy) as a biosimilar to pertuzumab (Perjeta) in breast cancer, based on a review of various attributes, including safety and efficacy data.

Data from the ASCENT-07 trial show an early trend toward improved overall survival with sacituzumab govitecan vs chemotherapy.
Sacituzumab Govitecan Misses PFS End Point in Metastatic Breast Cancer

November 11th 2025

How Dato-DXd and the TROPION Trials Are Transforming Solid Tumor Research
How Dato-DXd and the TROPION Trials Are Transforming Solid Tumor Research

November 8th 2025

The safety profile of palazestrant plus ribociclib in a phase 1b trial was comparable with prior reports of each individual agent.
Palazestrant Combo Shows Preliminary Activity in ER+/HER2– Breast Cancer

November 6th 2025

How Will the Continued Success of ADCs in Breast Cancer Be Propelled in the Future?
How Will the Continued Success of ADCs in Breast Cancer Be Propelled in the Future?

November 5th 2025

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Utility of the 21-Gene Recurrence Score in Node-Positive Breast Cancer

Utility of the 21-Gene Recurrence Score in Node-Positive Breast Cancer

February 11th 2021

ABSTRACT The 21-gene Recurrence Score (RS) assay has been validated as both a prognostic and predictive tool in node-negative (pN0), estrogen receptor–positive (ER+), HER2-negative (HER2–) breast cancer. A large body of evidence supports the clinical utility of the RS in the node positive (pN+) population as well. Retrospective analyses of archived tissue from multiple clinical trials have found the RS to be prognostic in both endocrine therapy (ET)-treated and chemotherapy-treated patients with pN+ disease. Distribution of RS results in pN+ patients have also been consistent with those of pN0 populations. Data from the SWOG 8814 trial and large population-based registries further support the prognostic and potential predictive value of the RS. Specifically, patients with 1 to 3 positive nodes and RS less than 18 derived negligible benefit from adjuvant chemotherapy in these studies. In the prospective West German Study Group PlanB and ADAPT trials, pN+ patients with RS less than 11 and RS ≤25, respectively, who were treated with ET alone experienced excellent outcomes. Finally, 5-year results of the RxPONDER clinical trial randomizing patients with 1 to 3 positive nodes and RS ≤25 to ET alone vs ET plus chemotherapy confirmed an absence of chemotherapy benefit in postmenopausal patients. Clinical practice guidelines support use of the RS in the pN+, ER+/HER2– population, and many institutions have adopted the RS to guide clinical decision-making, resulting in a net reduction of adjuvant chemotherapy use. This review highlights the existing data supporting the prognostic and predictive ability of the RS in pN+ disease, current practice patterns related to RS use in this population, and emerging applications.