HIPEC/CRS Confers No Benefit, Adds Risk in Colorectal Peritoneal Metastases

News
Video

Adding HIPEC to CRS did not show any added benefit but has shown increased toxicities in patients with colorectal peritoneal metastasis.

In an interview with CancerNetwork®, Muhammad Talha Waheed, MD, stated that it’s important to consider the risk vs benefit ratio when administering treatments to patients. At the 2025 Society of Surgical Oncology Annual Meeting (SSO), he presented a poster that showed “no added benefit” of hyperthermic intraperitoneal chemotherapy (HIPEC) added to cytoreduction surgery (CRS) in patients with colorectal cancer who have peritoneal metastasis.1

Waheed, a postdoctoral research fellow at City of Hope Comprehensive Cancer Center in Duarte, California, also spoke about the phase 3 PRODIGE-7 trial (NCT00769405), which evaluated the benefits and risks of adding HIPEC to CRS. That trial showed that at 30 days, grade 3 or higher adverse events (AEs) occurred in 42% of the CRS plus HIPEC group vs 32% in the CRS alone group (P = .083); at 60 days, grade 3 or higher AEs occurred in 26% vs 15% (P = .035).2

In Waheed’s study, results showed that HIPEC did not confer any added survival benefit: 1-year overall survival (OS) was 100% with CRS alone and 84.3% with CRS plus HIPEC (P = .006). Additionally, recurrence-free survival was similar in both groups.

Transcript:

When choosing a treatment option, there always has to be a discussion of risk vs benefit. When looking at the benefits specifically, our results report no added benefit of HIPEC. That begs the question, what is the benefit that you’re giving to these patients? At this point, we’re not able to comment on the risks because we were not able to compare the complications, but we’re in the process of abstracting those data. We will be able to compare the risks associated with either of the treatments, and we will report them in the paper.

Very interestingly, PRODIGE-7 did look at the complication rates between the 2 arms, which was the CRS alone treatment arm, and compared that with patients who underwent [CRS] with HIPEC [plus] oxaliplatin. They reported, although non-significant, that 30-day severe complications were higher in patients undergoing HIPEC. [Complications] 31 to 60 days after surgery were significantly higher in patients undergoing HIPEC. That begs the question: when you’re not able to provide any benefit, and there’s a risk or chance of increased complications for these patients, is there utility to still offer HIPEC?

The current data do support the use of HIPEC in [patients with] appendix cancer with peritoneal metastasis, so we continue to offer that for those patients. HIPEC, with some other agents, continues to be offered for [patients with] ovarian cancer at our center and nationwide. That is where I think this application—[CRS with HIPEC]—still is relevant.

References

  1. Waheed MT, Paz IB, Lwin T, et al. Impact of systematic discontinuation of mitomycin C (MMC) HIPEC for colorectal peritoneal metastasis (CRCPM) on oncologic outcomes at an NCI cancer center. Presented at SSO 2025; March 27-29, 2025; Tampa, FL.
  2. Quénet F, Elias D, Roca L, et al. Cytoreductive surgery plus hyperthermic intraperitoneal chemotherapy versus cytoreductive surgery alone for colorectal peritoneal metastases (PRODIGE 7): a multicentre, randomised, open-label, phase 3 trial. Lancet Oncol. 2021;22(2):256-266. doi:10.1016/S1470-2045(20)30599-4

Newsletter

Stay up to date on recent advances in the multidisciplinary approach to cancer.

Recent Videos
Future findings from a translational analysis of the OVATION-2 trial may corroborate prior clinical data with IMNN-001 in advanced ovarian cancer.
The dual high-affinity binding observed with ISB 2001 may avoid resistance mechanisms reported with other BCMA-targeted therapies.
The use of chemotherapy trended towards improved recurrence-free intervals in older patients with high-risk tumors as determined via the MammaPrint assay.
Use of a pharmacist-directed resource appears to improve provider confidence and adverse effect monitoring for patients undergoing infusion therapy.
Reshma L. Mahtani, DO, describes how updates from the DESTINY-Breast09, ASCENT-04, and VERITAC-2 trials may shift practices in the breast cancer field.
Stage IV lung cancer may be curable based on the success of the DREAM Program, according to thoracic surgeon, Ankit Bharat, MBBS,
Ankit Bharat, MBBS, a thoracic surgeon, discussed potential treatment emergent adverse effects or complications, as well as strategies for managing them.
Related Content