Publication: Benefit of Bevacizumab-Based Frontline Therapy in Patients with Metastatic Colorectal Cancer (mCRC): a Turkish Oncology Group Study
| dc.contributor.authors | Artaç M., Coşkun H.Ş., Dane F., Karabulut B., Korkmaz L., Karaağaç M., Çabuk D., Karabulut S., Faruk Aykan N., Doruk H., Avcı N., Turhal N.S. | |
| dc.date.accessioned | 2022-03-15T02:11:20Z | |
| dc.date.accessioned | 2026-01-11T17:46:49Z | |
| dc.date.available | 2022-03-15T02:11:20Z | |
| dc.date.issued | 2016 | |
| dc.description.abstract | Background: Several chemotherapy regimens using bevacizumab have been developed. Our goal was to investigate regimens that have demonstrated significant clinical activity in patients with metastatic colorectal cancer (mCRC). Materials and Methods: Six hundred and sixty six patients with mCRC who received first-line chemotherapy combination with bevacizumab were studied. Fluoropyrimidine (F) plus irinotecan (I)-based (FI-bev), F plus oxaliplatin (O)-based (FO-bev), and F-based (F-bev) treatment regimens were compared with respect to progression-free survival (PFS) and overall survival (OS). Results: The median PFS of FI-bev (n = 414) was 10.9 months (95 % CI 10–11.8), of FO-bev (n = 211) was 9.4 months (95 % CI 8.3–10.4), and of F-bev (n = 41) was 9.5 months (95 % CI 5.9–13.1) (p = 0.089). The median OS of FI-bev was 26.3 months (95 % CI 21.7–30.9), of FO-bev was 27 months (95 % CI 24.3–29.7), and of F-bev was 23.3 months (95 % CI 12.7–33.9) (p = 0.102). In KRAS wild-type patients, the median PFS of FI-bev group was significantly longer than FO-bev group (10.5 vs. 9.1 months, p = 0.006). The FI-bev group had better OS than FO-bev group with borderline significance (p = 0.058). The FI-bev group had significantly longer OS than F-bev group. Patients who underwent metastasectomy or those with Eastern Cooperative Oncology Group performance status (ECOG-PS) ≤1 had longer PFS and OS independent of the type of chemotherapy regimen. Conclusion: FI-bev may be the preferred frontline regimen for patients with KRAS wild-type mCRC. Metastasectomy and performance score were the strongest positive predictors of OS and PFS regardless of backbone chemotherapy regimen. © 2016, Springer Science+Business Media New York. | |
| dc.identifier.doi | 10.1007/s12029-016-9823-7 | |
| dc.identifier.issn | 19416628 | |
| dc.identifier.pubmed | 27126591 | |
| dc.identifier.uri | https://hdl.handle.net/11424/247654 | |
| dc.language.iso | eng | |
| dc.publisher | Humana Press Inc. | |
| dc.relation.ispartof | Journal of Gastrointestinal Cancer | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Fluoropyrimidine plus bevacizumab | |
| dc.subject | Irinotecan plus bevacizumab | |
| dc.subject | Metastatic colorectal cancer | |
| dc.subject | Oxaliplatin plus bevacizumab | |
| dc.title | Benefit of Bevacizumab-Based Frontline Therapy in Patients with Metastatic Colorectal Cancer (mCRC): a Turkish Oncology Group Study | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 272 | |
| oaire.citation.issue | 3 | |
| oaire.citation.startPage | 264 | |
| oaire.citation.title | Journal of Gastrointestinal Cancer | |
| oaire.citation.volume | 47 |
