Prospective, open-label, and observational study of cetuximab for metastatic colorectal carcinoma: The OPTIM1SE study

dc.contributor.authorYang, Tsia Sheng
dc.contributor.authorChen, Honghwa
dc.contributor.authorLin, Bowen
dc.contributor.authorKim, Taewon
dc.contributor.authorKim, Jong-gwang
dc.contributor.authorAhn, Joongbae
dc.contributor.authorLee, Myungah
dc.contributor.authorLin, Johnson
dc.contributor.authorHo, Gwofuang Fuang
dc.contributor.authorAnh, Le Tuan
dc.contributor.authorTemraz, Sally N.
dc.contributor.authorBurge, Matthew E.
dc.contributor.authorChua, Clarinda Wei Ling
dc.contributor.authorHuang, Jason
dc.contributor.authorPark, Young-suk
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Hematology Oncology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:46:15Z
dc.date.available2025-01-24T11:46:15Z
dc.date.issued2023
dc.description.abstractAim: 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.doihttps://doi.org/10.1111/ajco.13920
dc.identifier.eid2-s2.0-85149274335
dc.identifier.pmid36855017
dc.identifier.urihttp://hdl.handle.net/10938/30642
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofAsia-Pacific Journal of Clinical Oncology
dc.sourceScopus
dc.subject5-fluorouracil
dc.subjectCetuximab
dc.subjectFirst-line
dc.subjectMetastatic colorectal cancer
dc.subjectObservational study
dc.subjectAntineoplastic combined chemotherapy protocols
dc.subjectCamptothecin
dc.subjectColonic neoplasms
dc.subjectColorectal neoplasms
dc.subjectFemale
dc.subjectFluorouracil
dc.subjectHumans
dc.subjectLeucovorin
dc.subjectLiver neoplasms
dc.subjectMale
dc.subjectMiddle aged
dc.subjectProspective studies
dc.subjectProto-oncogene proteins p21(ras)
dc.subjectRectal neoplasms
dc.subjectTreatment outcome
dc.subjectFolinic acid
dc.subjectIrinotecan
dc.subjectOxaliplatin
dc.subjectAntineoplastic agent
dc.subjectProtein p21
dc.subjectAdult
dc.subjectArticle
dc.subjectAsthenia
dc.subjectClinical practice
dc.subjectColorectal carcinoma
dc.subjectComparative study
dc.subjectContinuous infusion
dc.subjectControlled study
dc.subjectDiarrhea
dc.subjectDistant metastasis
dc.subjectDrug efficacy
dc.subjectDrug safety
dc.subjectDrug tolerability
dc.subjectDrug use
dc.subjectElectronic medical record
dc.subjectFirst-line treatment
dc.subjectHuman
dc.subjectKras gene
dc.subjectLiver metastasis
dc.subjectMajor clinical study
dc.subjectMiddle east
dc.subjectNausea
dc.subjectNeutropenia
dc.subjectOncogene
dc.subjectOverall response rate
dc.subjectOverall survival
dc.subjectPatient monitoring
dc.subjectPatient participation
dc.subjectProgression free survival
dc.subjectProspective study
dc.subjectRash
dc.subjectRectum
dc.subjectRussian federation
dc.subjectStomatitis
dc.subjectTumor localization
dc.subjectColon tumor
dc.subjectColorectal tumor
dc.subjectLiver tumor
dc.subjectPathology
dc.subjectRectum tumor
dc.titleProspective, open-label, and observational study of cetuximab for metastatic colorectal carcinoma: The OPTIM1SE study
dc.typeArticle

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