Abstract 597P
Background
Hyperthermic Intraperitoneal Chemotherapy (HIPEC) is a procedure that involves cytoreductive surgery and delivering of high doses of chemotherapy into the abdominal cavity. It is mainly used to treat gastrointestinal cancers with peritoneal metastases. We analyzed our outcomes in terms of the immediate postoperative complications in the Intensity Care Unit (ICU) in patients submitted to the HIPEC procedure for advanced gastrointestinal tumors.
Methods
This is a cross-sectional retrospective study of patients diagnosed with gastrointestinal cancers submitted to the HIPEC procedure from January 2018 to June 2023, in a cancer institute. Clinical data was extracted from patient medical records and statistical analysis was performed using SPSS®, version 28.
Results
Eighty patients were included, with a median age of 53 years old. Thirty-seven (46%) were diagnosed with colon cancer, thirty-two (40%) with pseudomyxoma peritonei, seven (9%) with peritoneal mesothelioma, three (4%) with gastric cancer, and one (1%) with duodenal cancer. More than half of the patients were previously treated with induction chemotherapy, the majority using fluoropyrimidines. Regarding the chemotherapeutic agent used during the HIPEC procedure, 71 patients (89%) were treated with mitomycin, and the rest were treated with doxorubicin + cisplatin. The peritoneal cancer index (PCI) was between 0 and 39. All patients spent the immediate postoperative period in the Intensity Care Unit (ICU). The median stay in the ICU was 2 days [1-47 days]. Twenty-eight patients (35%) required vasopressors and/or invasive mechanical ventilation (IMV) postoperatively. Intraoperative blood loss correlates with the length of stay in the UCI, the total time of IMV, and the total time of vasopressor requirement. We also found a positive correlation between PCI and longer use of vasopressors, as well as between PCI and longer use of IMV.
Conclusions
This study is a report of “real world” use of the HIPEC procedure in advanced gastrointestinal cancers, regarding its immediate postoperative period. Despite its limitations, our data indicates that PCI and intraoperative blood loss might be predictors of complications in the ICU.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
556P - Predicting the efficacy of neoadjuvant chemoradiotherapy in rectal cancer patients based on dynamic tumor-informed ctDNA-MRD
Presenter: Weiwei Xiao
Session: Poster session 16
557P - Three-year update of real-world evaluation of ColonAiQ for colorectal cancer screening in asymptomatic individuals
Presenter: Baohua Wang
Session: Poster session 16
558P - Survival benefit of adjuvant chemotherapy based on molecular residual disease detection in resected colorectal liver metastases: Subgroup analysis from CIRCULATE-Japan GALAXY
Presenter: Kozo Kataoka
Session: Poster session 16
561P - Liquid biopsy tracking of immunotherapy-induced T cell dynamics in MSS colorectal and endometrial tumors
Presenter: Holger Heyn
Session: Poster session 16
562P - Acquired genomic alterations on first-line chemotherapy (CT) + cetuximab in advanced colorectal cancer (mCRC): Circulating tumor (ct)DNA analysis of the randomized phase II trial TIME-PRODIGE-28
Presenter: Valerie Boige
Session: Poster session 16
564P - Short-course radiotherapy combined with chemotherapy and PD-1 inhibitor in proficient mismatch repair or microsatellite stable (pMMR/MSS) low-lying early rectal cancer: Preliminary findings from a prospective, multi-center, phase II trial (TORCH-E)
Presenter: Fan Xia
Session: Poster session 16
565P - Neoadjuvant chemotherapy, excision, and observation for early rectal cancer: The phase II NEO trial (CCTG CO.28) results after minimum 3 years follow up
Presenter: Carl Brown
Session: Poster session 16