Prospective, open-label, and observational study of cetuximab for metastatic colorectal carcinoma: The OPTIM1SE study
| dc.contributor.author | Yang, Tsia Sheng | |
| dc.contributor.author | Chen, Honghwa | |
| dc.contributor.author | Lin, Bowen | |
| dc.contributor.author | Kim, Taewon | |
| dc.contributor.author | Kim, Jong-gwang | |
| dc.contributor.author | Ahn, Joongbae | |
| dc.contributor.author | Lee, Myungah | |
| dc.contributor.author | Lin, Johnson | |
| dc.contributor.author | Ho, Gwofuang Fuang | |
| dc.contributor.author | Anh, Le Tuan | |
| dc.contributor.author | Temraz, Sally N. | |
| dc.contributor.author | Burge, Matthew E. | |
| dc.contributor.author | Chua, Clarinda Wei Ling | |
| dc.contributor.author | Huang, Jason | |
| dc.contributor.author | Park, Young-suk | |
| dc.contributor.department | Internal Medicine | |
| dc.contributor.department | Division of Hematology Oncology | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:46:15Z | |
| dc.date.available | 2025-01-24T11:46:15Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Aim: The OPTIM1SE study observed long-term real-world outcomes of cetuximab-based infusional 5-fluorouracil (5-FU) regimens for first-line treatment of metastatic colorectal cancer (mCRC) across Asia-Pacific and Middle East regions, aiming to characterize their use, effectiveness, and safety in routine practice. Methods: OPTIM1SE was a prospective, open-label, observational study. Patients with untreated KRAS wild-type mCRC and distant metastases were treated per locally approved labels and monitored for 3 years via electronic medical records. The primary endpoint was the overall response rate (ORR). Secondary endpoints included safety, progression-free survival (PFS), and overall survival (OS). Results: From November 19, 2013, to June 30, 2016, 520 patients were enrolled in 51 sites. Patients were mostly male (61.2%), with a mean age of 58.5 (±12.0) years; 420 patients received leucovorin, 5-FU, and irinotecan–based regimens and 94 received leucovorin, 5-FU, and oxaliplatin. The most common primary tumor site was the rectum (38.8%), with liver metastases (65.0%). ORR was 45.4% (95% CI, 41.1%–49.7%), including 26 patients (5.0%) with a complete response. Median PFS was 9.9 months (95% CI, 8.2–11.0); median OS (mOS) was 30.8 months (95% CI, 27.9–33.6). Higher mOS was associated with tumors of left compared with right-sided origin (hazard ratio, 0.69 [95% CI, 0.49–0.99]); higher ORR was also associated with liver metastases compared with all other metastases (55.4% vs. 40.2%). Adverse events were consistent with the known safety profile of cetuximab. Conclusion: Cetuximab-based 5-FU regimens were effective first-line treatments for mCRC in routine practice, particularly in patients with left-sided disease and liver metastases only. © 2023 The Authors. Asia-Pacific Journal of Clinical Oncology published by John Wiley & Sons Australia, Ltd. | |
| dc.identifier.doi | https://doi.org/10.1111/ajco.13920 | |
| dc.identifier.eid | 2-s2.0-85149274335 | |
| dc.identifier.pmid | 36855017 | |
| dc.identifier.uri | http://hdl.handle.net/10938/30642 | |
| dc.language.iso | en | |
| dc.publisher | John Wiley and Sons Inc | |
| dc.relation.ispartof | Asia-Pacific Journal of Clinical Oncology | |
| dc.source | Scopus | |
| dc.subject | 5-fluorouracil | |
| dc.subject | Cetuximab | |
| dc.subject | First-line | |
| dc.subject | Metastatic colorectal cancer | |
| dc.subject | Observational study | |
| dc.subject | Antineoplastic combined chemotherapy protocols | |
| dc.subject | Camptothecin | |
| dc.subject | Colonic neoplasms | |
| dc.subject | Colorectal neoplasms | |
| dc.subject | Female | |
| dc.subject | Fluorouracil | |
| dc.subject | Humans | |
| dc.subject | Leucovorin | |
| dc.subject | Liver neoplasms | |
| dc.subject | Male | |
| dc.subject | Middle aged | |
| dc.subject | Prospective studies | |
| dc.subject | Proto-oncogene proteins p21(ras) | |
| dc.subject | Rectal neoplasms | |
| dc.subject | Treatment outcome | |
| dc.subject | Folinic acid | |
| dc.subject | Irinotecan | |
| dc.subject | Oxaliplatin | |
| dc.subject | Antineoplastic agent | |
| dc.subject | Protein p21 | |
| dc.subject | Adult | |
| dc.subject | Article | |
| dc.subject | Asthenia | |
| dc.subject | Clinical practice | |
| dc.subject | Colorectal carcinoma | |
| dc.subject | Comparative study | |
| dc.subject | Continuous infusion | |
| dc.subject | Controlled study | |
| dc.subject | Diarrhea | |
| dc.subject | Distant metastasis | |
| dc.subject | Drug efficacy | |
| dc.subject | Drug safety | |
| dc.subject | Drug tolerability | |
| dc.subject | Drug use | |
| dc.subject | Electronic medical record | |
| dc.subject | First-line treatment | |
| dc.subject | Human | |
| dc.subject | Kras gene | |
| dc.subject | Liver metastasis | |
| dc.subject | Major clinical study | |
| dc.subject | Middle east | |
| dc.subject | Nausea | |
| dc.subject | Neutropenia | |
| dc.subject | Oncogene | |
| dc.subject | Overall response rate | |
| dc.subject | Overall survival | |
| dc.subject | Patient monitoring | |
| dc.subject | Patient participation | |
| dc.subject | Progression free survival | |
| dc.subject | Prospective study | |
| dc.subject | Rash | |
| dc.subject | Rectum | |
| dc.subject | Russian federation | |
| dc.subject | Stomatitis | |
| dc.subject | Tumor localization | |
| dc.subject | Colon tumor | |
| dc.subject | Colorectal tumor | |
| dc.subject | Liver tumor | |
| dc.subject | Pathology | |
| dc.subject | Rectum tumor | |
| dc.title | Prospective, open-label, and observational study of cetuximab for metastatic colorectal carcinoma: The OPTIM1SE study | |
| dc.type | Article |
Files
Original bundle
1 - 1 of 1