6533b859fe1ef96bd12b7873

RESEARCH PRODUCT

Phase I Study of Definitive Radio-chemotherapy with Cisplatin, 5-Fluorouracil and Cetuximab for Unresectable Locally Advanced Esophageal Cancer.

Annika PanznerMarkus MoehlerPeter HunoldHeinz SchmidbergerDirk RadesVisvakanth SivanathanAnnett Maderer

subject

OncologyMaleCancer Researchmedicine.medical_specialtyEsophageal NeoplasmsMaximum Tolerated Dosemedicine.medical_treatmentPhases of clinical researchCetuximabAntineoplastic AgentsLoading dose030218 nuclear medicine & medical imaging03 medical and health sciences0302 clinical medicineInternal medicineAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansAgedCisplatinChemotherapyCetuximabbusiness.industryGeneral MedicineChemoradiotherapyEsophageal cancerMiddle Agedmedicine.diseaseRadiation therapyTreatment OutcomeOncologyFluorouracil030220 oncology & carcinogenesisFemaleFluorouracilCisplatinbusinessmedicine.drug

description

Background/aim Prognoses of patients receiving radio-chemotherapy with 5-fluorouracil (5-FU) and cisplatin for unresectable esophageal cancer may be improved with the addition of cetuximab. This phase I study aimed to define the maximum tolerated dose of 5-FU when combined with cisplatin, cetuximab and radiotherapy. Patients and methods Treatment included 59.4 Gy of radiotherapy concurrently with two courses of cisplatin (20 mg/m2, d1-4) and 5-FU (dose level 0: 500 mg/m2, dose level 1: 750 mg/m2, d1-4; dose level 2: 1,000 mg/m2, d1-4), followed by two courses of chemotherapy. Cetuximab was given for 14 weeks (400 mg/m2 loading dose followed by 250 mg/m2 weekly). Results At dose level 1 (n=3) and 2 (n=3), no patient experienced a dose-limiting toxicity. Minor treatment modifications were due to organization or request by physicians/patients. At dose level 2, only five grade 3 adverse events occurred. Conclusion Dose level 2 appears safe and is used in a subsequent randomized phase II study.

10.21873/anticanres.11620https://pubmed.ncbi.nlm.nih.gov/28476848