#888 Real-world treatment patterns in recurrent or advanced endometrial cancer patients who initiated first-line systemic therapy in 5 European countries: a retrospective chart review study

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Publicado en:International Journal of Gynecological Cancer vol. 33, no. Suppl 3 (Sep 2023), p. A186
Autor Principal: Kelkar, Sneha S
Outros autores: Prabhu, Vimalanand S, Zhang, Jingchuan, Ogando, Yoscar M, Grall, Véronique, Marth, Christian
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Elsevier Limited
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022 |a 1048-891X 
022 |a 1525-1438 
024 7 |a 10.1136/ijgc-2023-ESGO.383  |2 doi 
035 |a 2869209734 
045 2 |b d20230901  |b d20230930 
100 1 |a Kelkar, Sneha S 
245 1 |a #888 Real-world treatment patterns in recurrent or advanced endometrial cancer patients who initiated first-line systemic therapy in 5 European countries: a retrospective chart review study 
260 |b Elsevier Limited  |c Sep 2023 
513 |a Journal Article 
520 3 |a Introduction/BackgroundNovel therapies are being investigated for first-line use in recurrent or advanced endometrial cancer (aEC) patients in Europe, however, country-specific real-world treatment patterns with conventional treatments are not well documented.MethodologyEndometrial Cancer Health Outcomes-Europe-First-Line (ECHO-EU-1L) is a retrospective chart review study in recurrent or aEC patients in United Kingdom (UK), France (FR), Germany (GE), Italy (IT), and Spain (SP). Physicians extracted de-identified data from medical records of adult female patients initiating first-line therapy between 1/JUL/2016 and 31/MAR/2020 after aEC diagnosis. Ethics approval and informed consent waivers were obtained.ResultsOverall, 57 physicians provided data for 242 patients (UK=49, FR=49, GE=48, IT=48, SP=48) with a median age of 69 years at aEC diagnosis, 49.2% with endometroid carcinoma, and 23.6% with ECOG≥2 at treatment start. Carboplatin-paclitaxel was the most prescribed first-line regimen in all countries (UK=51.0%, FR=79.6%, GE=58.3%, IT=66.7%, SP=81.3%). Second preference varied: cisplatin-paclitaxel in UK (28.6%), cisplatin-5-fluorouracil in FR (6.1%), bevacizumab-carboplatin-paclitaxel in GE (18.8%), carboplatin monotherapy in IT (12.5%), and doxorubicin-liposomal, megestrol acetate, or paclitaxel in SP (4.2% each). Overall, physicians prescribed >20 different regimens in first-line. Overall, 95% of patients discontinued first-line treatment, mostly due to progression (cross-country range: 40.0–59.2%), regimen completion (26.7–49.0%), and maximum clinical benefit reached (6.1–35.6%). Median time to discontinuation was 5.2 months (95% confidence interval: 4.9–5.5) (UK=4.3, FR=5.4, GE=5.5, IT=6.3, SP=5.3). Overall, 31.3–54.2% of patients initiated second-line treatment.ConclusionIn European recurrent or aEC patients prior to 2021, guideline-recommended carboplatin-paclitaxel was a prevalent first-line regimen, however there were marked cross-country variations in other regimens selected and overall treatment approach. Novel therapies are needed to help streamline treatment options for these patients.DisclosuresFunding for this research was provided by Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA and Eisai Inc., Nutley, NJ, USA. Sneha Kelkar and Yoscar Ogando are employees of OPEN Health, Bethesda, MD, USA, who were paid consultants of Merck Sharp & Dohme LLC a subsidiary of Merck & Co., Inc., Rahway, NJ, USA. in connection with the development of this abstract, study design, management, and statistical analysis for the study. Vimalanand Prabhu and spouse are employees of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA, and shareholder of Merck & Co., Inc., Rahway, NJ, USA. Jingchuan Zhang is an employee of Eisai Inc., Nutley, NJ, USA. Véronique Grall is an employee of M3 (EU), Abingdon, England, a subcontractor to OPEN Health, who were paid consultants of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA in the data collection for the study. Christian Marth is an employee of Medical University Innsbruck, Innsbruck, Austria, which has received funding for clinical research support from Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA, and reports honoraria/consulting fees from Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA. 
610 4 |a Merck & Co Inc Merck Sharp & Dohme 
651 4 |a United States--US 
651 4 |a United Kingdom--UK 
651 4 |a Europe 
653 |a Endometrial cancer 
653 |a Cancer therapies 
653 |a Employees 
653 |a Monoclonal antibodies 
653 |a Physicians 
700 1 |a Prabhu, Vimalanand S 
700 1 |a Zhang, Jingchuan 
700 1 |a Ogando, Yoscar M 
700 1 |a Grall, Véronique 
700 1 |a Marth, Christian 
773 0 |t International Journal of Gynecological Cancer  |g vol. 33, no. Suppl 3 (Sep 2023), p. A186 
786 0 |d ProQuest  |t Health & Medical Collection 
856 4 1 |3 Citation/Abstract  |u https://www.proquest.com/docview/2869209734/abstract/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch