دورية أكاديمية

HIPECT4: multicentre, randomized clinical trial to evaluate safety and efficacy of Hyperthermic intra-peritoneal chemotherapy (HIPEC) with Mitomycin C used during surgery for treatment of locally advanced colorectal carcinoma.

التفاصيل البيبلوغرافية
العنوان: HIPECT4: multicentre, randomized clinical trial to evaluate safety and efficacy of Hyperthermic intra-peritoneal chemotherapy (HIPEC) with Mitomycin C used during surgery for treatment of locally advanced colorectal carcinoma.
المؤلفون: Arjona-Sánchez, A, Barrios, P, Boldo-Roda, E, Camps, B, Carrasco-Campos, J, Concepción Martín, V, García-Fadrique, A, Gutiérrez-Calvo, A, Morales, R, Ortega-Pérez, G, Pérez-Viejo, E, Prada-Villaverde, A, Torres-Melero, J, Vicente, E, Villarejo-Campos, P, Sánchez-Hidalgo, J M, Casado-Adam, A, García-Martin, Ruben, Medina, Manuel, Caro, T
المصدر: BMC Cancer; 2/13/2018, Vol. 18, p183-183, 1p
مصطلحات موضوعية: ANTINEOPLASTIC antibiotics, MITOMYCINS, COLON tumors, COMBINED modality therapy, COMPARATIVE studies, RESEARCH methodology, MEDICAL cooperation, RECTUM tumors, RESEARCH, STATISTICAL sampling, THERMOTHERAPY, EVALUATION research, RANDOMIZED controlled trials, TREATMENT effectiveness, KAPLAN-Meier estimator, THERAPEUTICS, TUMOR treatment
مستخلص: Background: Local relapse and peritoneal carcinomatosis (PC) for pT4 colon cancer is estimated in 15,6% and 36,7% for 12 months and 36 months from surgical resection respectively, achieving a 5 years overall survival of 6%. There are promising results using prophylactic HIPEC in this group of patients, and it is estimated that up to 26% of all T4 colon cancer could benefit from this treatment with a minimal morbidity. Adjuvant HIPEC is effective to avoid the possibility of peritoneal seeding after surgical resection. Taking into account these results and the cumulative experience in HIPEC use, we will lead a randomized controlled trial to determine the effectiveness and safety of adjuvant treatment with HIPEC vs. standard treatment in patients with colon cancer at high risk of peritoneal recurrence (pT4).Methods/design: The aim of this study is to determine the effectiveness and safety of adjuvant HIPEC in preventing the development of PC in patients with colon cancer with a high risk of peritoneal recurrence (cT4). This study will be carried out in 15 Spanish HIPEC centres. Eligible for inclusion are patients who underwent curative resection for cT4NxM0 stage colon cancer. After resection of the primary tumour, 200 patients will be randomized to adjuvant HIPEC followed by routine adjuvant systemic chemotherapy in the experimental arm, or to systemic chemotherapy only in the control arm. Adjuvant HIPEC will be performed simultaneously after the primary resection. Mitomycin C will be used as chemotherapeutic agent, for 60 min at 42-43 °C. Primary endpoint is loco-regional control (LC) in months and the rate of loco-regional control (%LC) at 12 months and 36 months after resection.Discussion: We assumed that adjuvant HIPEC will reduce the expected absolute risk of peritoneal recurrence from 36% to 18% at 36 months for T4 colon-rectal carcinoma.Trial Registration: NCT02614534 ( clinicaltrial.gov ) Nov-2015. [ABSTRACT FROM AUTHOR]
Copyright of BMC Cancer is the property of BioMed Central and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:14712407
DOI:10.1186/s12885-018-4096-0