TerSera's Study Reveals Efficacy of Goserelin for Breast Cancer
TerSera's Key Findings on Goserelin for Women with Breast Cancer
TerSera Therapeutics LLC has made significant contributions to the understanding of goserelin, an important drug in treating breast cancer, particularly in premenopausal women. They recently presented new analyses demonstrating the effectiveness of goserelin dosages of 3.6 mg and 10.8 mg during a poster session at a prominent breast cancer symposium.
The Importance of Real-World Data
This study utilized real-world data derived from patient records. By comparing the two dosages of goserelin, the research aimed to better understand treatment outcomes for women battling breast cancer. This kind of observational study is crucial as it reflects actual experiences of patients rather than controlled clinical trial conditions, providing insights into effectiveness in everyday clinical practice.
Understanding the Study Design
The retrospective study involved structured de-identified patient-level data, focusing on the event-free survival (rwEFS) rates for goserelin 3.6 mg versus 10.8 mg. Specifically, researchers sought to determine whether administering the higher dose every 12 weeks could be as effective as the lower dose given more frequently every month.
Results Highlight the Effectiveness of Goserelin
The results showed promising findings, with the 12-month rwEFS rates being 76.6% for the 3.6 mg dosage compared to 79.2% for the 10.8 mg dosage. This slight difference supports the idea that the higher dose may not only be effective, but could potentially simplify treatment regimens for patients.
Implications for Treatment Duration
Further evaluation of the data indicated that patients on the 10.8 mg dosage were more likely to remain on treatment for longer periods, with 51.2% continuing after one year compared to 39.6% of those taking 3.6 mg. This retention rate could lead to improved outcomes for women participating in breast cancer treatment.
Expert Commentary on Study Findings
Dr. Kelly E. McCann, an assistant clinical professor, emphasized the significance of ovarian function suppression (OFS) in the treatment of hormone-sensitive breast cancer. She pointed out that while ZOLADEX 3.6 mg is currently the only FDA-approved GnRHa for these patients, the new findings suggest that administering the 10.8 mg dose could equally benefit these women.
Safety and Usage Indications for Goserelin
Goserelin, available in both 3.6 mg and 10.8 mg dosages, is indicated for various conditions such as the management of hormone-sensitive breast cancer and endometriosis. Importantly, it is crucial for healthcare providers to assess the potential risks and benefits of using goserelin, particularly concerning safety considerations for users who may have hypersensitivity.
Patient Monitoring and Reporting Side Effects
Patients using goserelin are encouraged to report any side effects experienced during the treatment process. Awareness and proactive communication with healthcare providers can significantly improve individual patient care.
The Broader Impact of Breast Cancer Statistics
This new information from TerSera highlights the necessity for continued research in the field of breast cancer, particularly for younger women diagnosed with hormone-positive breast cancer. The statistics are alarming, as they show a rising number of cases among women under 50, with younger women facing more aggressive forms of the disease.
Commitment to Advancing Breast Cancer Therapies
TerSera Therapeutics, founded in 2016, remains dedicated to pioneering effective treatment options for patients experiencing challenging health conditions, including breast cancer. The company focuses not only on commercializing unique therapeutics but also on amplifying positive outcomes for patients through meaningful clinical research.
Frequently Asked Questions
What is goserelin used for?
Goserelin is used to treat breast cancer, prostate cancer, and certain gynecological disorders by suppressing ovarian function.
What were the findings of the recent TerSera study?
The study found that the 10.8 mg goserelin dosage every 12 weeks showed comparable effectiveness to the 3.6 mg dose every 4 weeks.
Why is real-world data important in clinical studies?
Real-world data reflects patient experiences outside clinical trial conditions, providing a better understanding of treatment effectiveness in routine clinical practice.
What should patients do if they experience side effects from goserelin?
Patients should report any side effects to their healthcare provider to facilitate monitoring and improve care.
How does TerSera contribute to breast cancer treatment advancements?
TerSera is committed to research and developing innovative therapies that enhance treatment options for patients with breast cancer and other serious conditions.
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