The use of regorafenib for patients with refractory metastatic colorectal cancer in clinical practice

التفاصيل البيبلوغرافية
العنوان: The use of regorafenib for patients with refractory metastatic colorectal cancer in clinical practice
المؤلفون: Yoon SE, Lee SJ, Lee J, Park SH, Park JO, Lim HY, Kang WK, Park YS, Kim ST
المصدر: OncoTargets and Therapy, Vol Volume 12, Pp 225-231 (2018)
بيانات النشر: Dove Medical Press, 2018.
سنة النشر: 2018
مصطلحات موضوعية: Regorafenib, colorectal cancer, initial dose, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, lcsh:RC254-282
الوصف: Sang Eun Yoon, Su Jin Lee, Jeeyun Lee, Se Hoon Park, Joon Oh Park, Ho Yeong Lim, Won Ki Kang, Young Suk Park, Seung Tae Kim Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea Aim: Patients in clinical practice are relatively vulnerable compared to those enrolled in clinical trials. We focused on analyzing the pattern of regorafenib use in routine clinical practice, which included initial starting dose and follow-up schedule. We also evaluated the efficacy and safety according to clinical regimen.Methods: We retrospectively reviewed the medical records of 134 Korean heavily pretreated metastatic colorectal cancer (mCRC) patients who had received regorafenib monotherapy as salvage treatment in routine clinical practice between January 2014 and January 2018.Results: Among the 134 mCRC patients, the median age was 55 years (range, 22–80 years), and 51% had previously received four or more chemotherapy treatments. Thirty-eight (28.3%) patients had more than three metastatic lesions. As an initial starting dose, 120mg regorafenib was mostly frequently used (n=65, 48.5%), followed by 80 mg (32.8%) and 160mg (18.7%). The first follow-up after regorafenib initiation was most frequently at 28 days (45.5%), followed by 14 days (29.9%), 7 days (13.4%), and 21 days (11.2%). There was no significant difference in response rate according to initial dose of regorafenib (80 mg vs 120 mg vs 160 mg, 4.5% vs 1.5% vs 4.0%, P=0.596) or disease control rate (80 mg vs 120 mg vs 160 mg, 38.6% vs 29.2% vs 31.6%, P=0.299). Progression-free survival did not differ according to initial dose (80 mg vs 120 mg vs 160 mg, 2.8 months [95% CI 2.1–3.5] vs 2.2 months [95% CI 1.7–2.8] vs 1.9 months [95% CI 1.3–2.4], P=0.076). Grade 3/4 adverse events occurred in 17 (12.7%) patients and were not related to initial dose of regorafenib (P=0.126).Conclusion: Here, we present efficacy and safety data according to different initial doses of regorafenib in clinical practice. These data may provide useful information when using regorafenib for refractory mCRC in clinical practice. Keywords: regorafenib, colorectal cancer, initial dose
اللغة: English
تدمد: 1178-6930
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doajarticles::294296b1853430c7244300043340ba8f
https://www.dovepress.com/the-use-of-regorafenib-for-patients-with-refractory-metastatic-colorec-peer-reviewed-article-OTT
حقوق: OPEN
رقم الأكسشن: edsair.doajarticles..294296b1853430c7244300043340ba8f
قاعدة البيانات: OpenAIRE