(Lung Cancer) Durvalumab Plus Olaparib Combination Achieves 10.5% ORR
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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.
- June 3, 2019
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Durvalumab Plus Olaparib in Relapsed Small Cell Lung Cancer: ORR 10.5%
On May 4, 2019, the Journal of Thoracic Oncology published Phase 2 trial results evaluating the efficacy and safety of the durvalumab plus olaparib combination therapy in patients with relapsed small cell lung cancer (SCLC).
Trial Design
This was a single-arm Phase 2 trial administering durvalumab plus olaparib every four weeks to patients with relapsed SCLC, with objective response rate (ORR) as the primary endpoint.
Background: Although immune checkpoint inhibitors demonstrate high anti-cancer efficacy, their effectiveness in SCLC is limited. Combining immune checkpoint inhibitors with PARP inhibitors was hypothesized to improve sensitivity.
Efficacy Results
Among 20 enrolled patients, 19 were evaluable:
- ORR: 10.5%
- Partial response: 1 patient
- Complete response: 1 patient
- Stable disease maintained for ≥6 months
Safety Profile
Most common adverse events confirmed across the majority of patients: anemia, lymphopenia, and leukopenia.
Conclusions
Based on the Phase 2 trial results, this combination therapy did not meet the pre-specified target objective response rate.
Source: Durvalumab in Combination with Olaparib in Patients with Relapsed Small Cell Lung Cancer: Results from a Phase II Study. J Thorac Oncol. 2019 May 4. pii: S1556-0864(19)30361-2. doi: 10.1016/j.jtho.2019.04.026.
Tags: #SmallCellLungCancer #LungCancer
- Clinical trial drug
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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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