Efficacy and safety of folfiri plus aflibercept in second-line treatment of metastatic colorectal cancer: Real-life data from Turkish oncology group
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info:eu-repo/semantics/openAccessAttribution-NonCommercial-ShareAlike 4.0 Internationalhttps://creativecommons.org/licenses/by-nc-sa/4.0/Date
2022Author
Erol, CihanŞendur, Mehmet Ali Nahit
Bilgetekin, İrem
Bayır Garbioğlu, Duygu
Hamdard, Jamshid
Akbaş, Sinem
Hizal, Mutlu
Arslan, Çağatay
Sevinç, Alper
Küçükarda, Ahmet
Erdem, Dilek
Kahraman, Seda
Çakır, Emre
Demirkıran, Aykut
On, Sercan
Doğan, İzzet
Erdoğan, Atike Pınar
Koca, Sinan
Kubilay, Pınar
Eren, Orhan Önder
Çılbır, Ebru
Çelik, Emir
Araz, Murat
Tataroğlu Özyükseler, Deniz
Yıldırım, Mahmut Emre
Bahçeci, Aykut
Taşkaynatan, Halil
Oyman, Abdilkerim
Deniz, Gülhan İpek
Menekşe, Serkan
Kut, Engin
Gülmez, Ahmet
Sakin, Abdullah
Nayır, Erdinç
Acar, Ramazan
Şen, Erdem
İnal, Ali
Turhal, Serdar
Kaya, Ali Osman
Paydaş, Semra
Taştekin, Didem
Hacıbekiroğlu, İlhan
Çinçin, İrfan
Bilici, Ahmet
Mandel, Nil Molinas
Şener Dede, Didem
Akıncı, Muhammed Bülent
Öksüzoğlu, Berna
Uncu, Doğan
Yalçın, Bülent
Artaç, Mehmet
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Erol, C., Şendur, M. A. N., Bilgetekin, İ., Bayır Garbioğlu, D., Hamdard, J., Akbaş, S. ... Artaç, M. (2022). Efficacy and safety of folfiri plus aflibercept in second-line treatment of metastatic colorectal cancer: Real-life data from Turkish oncology group. Journal of Cancer Research and Therapeutics, 18, S347-S353. https://doi.org/10.4103/jcrt.jcrt_1104_21Abstract
Aims: The addition of aflibercept to the fluorouracil and irinotecan (FOLFIRI) regimen significantly improved clinical outcomes in patients with metastatic colorectal cancer (CRC) previously treated with oxaliplatin. We aimed to investigate the efficacy and safety of second-line FOLFIRI and aflibercept combination in patients with metastatic CRC in real-life experience. Materials and Methods: Four hundred and thirty-three patients who treated with FOLFIRI and aflibercept in the second-line were included in the study. The clinical and pathological features of the patients were recorded retrospectively. Survival (overall and progression-free survival [PFS]), response rates, and safety data were analyzed. Results: The median age was 61. Majority of patients (87.5%) received first-line bevacizumab and 10.1% of patients received anti-epidermal growth factor receptor agents. About 80% of patients had KRAS, 18.6% of patients had NRAS, and 6.4% of patients had BRAF mutations. The median OS was 11.6 months (95% confidence interval [CI], 10.6-12.6) and the median PFS was 6 months (95% CI, 5.5-6.5). About 4.6% of patients had complete response and 30.6% of patients had partial response as best tumor response. Grade 1-2 toxicities were seen in 33.4% of patients, while grade 3-4 toxicities were recorded in 27% of patients. Eight patients (2%) died due to treatment toxicity. Conclusions: Overall and PFS were similar in routine clinical practice compared to phase III pivotal VELOUR trial. However, response rates were found to be higher. It was observed that there were fewer adverse events compared to the VELOUR trial.
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