Publication: Kras-mutation influences outcomes for palliative primary tumor resection in advanced colorectal cancer-a Turkish Oncology Group study
| dc.contributor.authors | Korkmaz, Levent; Coskun, Hasan Senol; Dane, Faysal; Karabulut, Bulent; Karaagac, Mustafa; Cabuk, Devrim; Karabulut, Senem; Aykan, Nuri Faruk; Doruk, Hatice; Avci, Nilufer; Turhal, Nazim Serdar; Artac, Mehmet | |
| dc.date.accessioned | 2022-03-12T22:27:49Z | |
| dc.date.accessioned | 2026-01-11T13:20:40Z | |
| dc.date.available | 2022-03-12T22:27:49Z | |
| dc.date.issued | 2018 | |
| dc.description.abstract | Purpose: We aimed to investigate the prognostic effect of primary tumor resection (PTR) prior to bevacizumab-based treatments in unresectable metastatic colorectal cancer (mCRC). Methods: We retrospectively collected 341 mCRC cases with unresectable metastases at diagnosis. PTR was performed in 210 cases (the surgery group) and the other patients (n = 131) were followed without PTR (the no-surgery group). All the patients were treated with bevacizumab combined chemotherapy regimens. Results: The median progression free survival (PFS) of the surgery group was 10.4 months (95% CI: 8.9-11.9), which was significantly better than that of the no-surgery group (7.6 months, 95% CI: 6.4-8.8, P = 0.000). The median overall survival (OS) of the surgery group was longer than that of the no-surgery group (27.4 months vs. 18.3 months, respectively, P = 0.000). The median PFS and OS of the surgery group were 10.4 months and 28.2 months, which were significantly longer than that of the no-surgery group in Kras-mutant patients (7.8 months and 18.3 months; P = 0.004, P = 0 .028, respectively). There was no difference in terms of PFS and OS between the surgery and the no-surgery groups in Kras-wild type patients. Conclusion: Palliative PTR may improve the survival outcomes for unresectable mCRC patients. PTR may be preferred, particularly in Kras-mutant patients. | |
| dc.identifier.doi | 10.1016/j.suronc.2018.05.032 | |
| dc.identifier.eissn | 1879-3320 | |
| dc.identifier.issn | 0960-7404 | |
| dc.identifier.pubmed | 30217306 | |
| dc.identifier.uri | https://hdl.handle.net/11424/235248 | |
| dc.identifier.wos | WOS:000444463900023 | |
| dc.language.iso | eng | |
| dc.publisher | ELSEVIER SCI LTD | |
| dc.relation.ispartof | SURGICAL ONCOLOGY-OXFORD | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Metastatic colorectal cancer | |
| dc.subject | Bevacizumab | |
| dc.subject | Primary tumor resection | |
| dc.subject | UNRESECTABLE SYNCHRONOUS METASTASES | |
| dc.subject | RANDOMIZED PHASE-III | |
| dc.subject | POOLED ANALYSIS | |
| dc.subject | BEVACIZUMAB | |
| dc.subject | CHEMOTHERAPY | |
| dc.subject | COMBINATION | |
| dc.subject | SURVIVAL | |
| dc.subject | EFFICACY | |
| dc.subject | SURGERY | |
| dc.subject | THERAPY | |
| dc.title | Kras-mutation influences outcomes for palliative primary tumor resection in advanced colorectal cancer-a Turkish Oncology Group study | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 489 | |
| oaire.citation.issue | 3 | |
| oaire.citation.startPage | 485 | |
| oaire.citation.title | SURGICAL ONCOLOGY-OXFORD | |
| oaire.citation.volume | 27 |
