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آخر تحديث: 2016-11-19

(Breast Cancer) Verzenio Plus Keytruda: Is It Effective?

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فريق Medical Supporter
فريق تنسيق طبي دولي ومراجعة تحريرية
(Breast Cancer) Verzenio Plus Keytruda: Is It Effective?

(Breast Cancer) Verzenio Plus Keytruda: Is It Effective?

Medical Supporter — إشعار معلوماتي

هذه المقالة ملخص لمعلومات طبية دولية وليست نصيحة طبية، ولا يمكن أن تحل محل تشخيص طبيبك المعالج أو خطة العلاج. المعلومات المعروضة مجمّعة من منشورات عامة وبيانات رسمية لكبرى المؤسسات الطبية اليابانية؛ وتختلف ملاءمة ونتائج أي علاج من مريض لآخر ويجب أن يقيّمها طبيب مؤهل لكل حالة على حدة.

يجب أن يقيّم أي خطة علاج محددة طبيب مرخّص في اليابان

From May 29–31, 2020, Dr. Hope S. Rugo presented at the ASCO 2020 Virtual Scientific Program interim analysis results from a Phase 1b clinical trial evaluating the CDK4/6 inhibitor Verzenio (abemaciclib) combined with the PD-1 antibody Keytruda (pembrolizumab) in previously treated patients with hormone receptor (HR)-positive, HER2-negative locally advanced or metastatic breast cancer.

This Phase 1b trial was an open-label, multi-center study enrolling 28 patients with previously treated HR+, HER2-negative locally advanced or metastatic breast cancer. Patients received Verzenio 150 mg twice daily plus Keytruda 200 mg on a 21-day cycle. The primary endpoint was safety; secondary endpoints included objective response rate (ORR), progression-free survival (PFS), and overall survival (OS).

The trial was initiated based on confirmed anti-tumor activity of Verzenio monotherapy or aromatase inhibitor plus fulvestrant in HR+, HER2-negative locally advanced or metastatic breast cancer patients, as well as preclinical data demonstrating anti-tumor activity of Verzenio plus Keytruda in mouse models.

Results:

Primary endpoint safety: Grade 3–4 adverse events included neutropenia (29%, N=8), AST elevation (18%, N=5), diarrhea (11%, N=3), and ALT elevation (11%, N=3). Safety findings were consistent with previously known Verzenio adverse events; no new safety signals were identified.

Secondary endpoints:

  • Objective response rate (ORR): 29%
  • Disease control rate (DCR): 82%
  • Median PFS: 8.9 months
  • Median OS: 26.3 months

Conclusion: Based on the interim analysis, Dr. Rugo concluded that Verzenio plus Keytruda showed numerically favorable ORR, PFS, and OS compared to historical Verzenio monotherapy data, though no statistically significant difference was confirmed.

Disclaimer: Medical Supporter translates overseas clinical trial data and pharmaceutical information for informational purposes only. This does not constitute encouragement to participate in clinical trials or use any new drug. Translation materials are for reference only. Please consult your healthcare provider for medical decisions.

Source: A phase Ib study of abemaciclib in combination with pembrolizumab for patients with hormone receptor positive (HR+), human epidermal growth factor receptor 2 negative (HER2-) locally advanced or metastatic breast cancer (MBC) (NCT02779751): Interim results. (2020 ASCO Virtual Scientific Program, Abstract No: 1051)

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هل تفكر في تلقّي العلاج في اليابان؟ هل تحتاج إلى معلومات ومساعدة؟

نساعدك في تنظيم المعلومات اللازمة للسفر الطبي إلى اليابان، والتواصل مع المؤسسات الطبية اليابانية، وترتيب استشارة رأي ثانٍ.الاستشارة الأولى مجانية؛ سيساعدك المستشار على توضيح الخطوات التالية.

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