Abstract
Simple SummaryPressurized IntraPeritoneal Aerosol Chemotherapy (PIPAC) is an emerging treatment modality for patients with peritoneal cancer with good safety profile and promising early response rates. The aim of this study was to analyze survival and surrogates for oncological response after PIPAC ± systemic chemotherapy for appendiceal tumours. Median overall survival of this cohort was 30 months from time of diagnosis and 22 months from PIPAC1 (per protocol) comparing favorably with 20.4 months of OS reported for patients with palliative chemotherapy alone. However, without prospective comparative data, the role of PIPAC for appendicular cancer with peritoneal metastases remains unclear.Background The aim of this study was to analyse survival and surrogates for oncological response after PIPAC for appendiceal tumours. Methods This retrospective cohort study included consecutive patients with appendiceal peritoneal metastases (PM) treated in experienced PIPAC centers. Primary outcome measure was overall survival (OS) from the date of diagnosis of PM and from the start of PIPAC. Predefined secondary outcome included radiological response (RECIST criteria), repeat laparoscopy and peritoneal cancer index (PCI), histological response assessed by the Peritoneal regression grading system (PRGS) and clinical response. Results Final analysis included 77 consecutive patients (208 PIPAC procedures) from 15 centres. Median OS was 30 months (23.00–46.00) from time of diagnosis and 19 months (13.00–28.00) from start of PIPAC. 35/77 patients (45%) had ≥3 procedures (pp: per protocol). Objective response at PIPAC3 was as follows: RECIST: complete response 4 (11.4%), 11 (31.4%) partial/stable; mean PRGS at PIPAC3: 1.8 ± 0.9. Median PCI: 21 (IQR 18–27) vs. 22 (IQR 17–28) at baseline (p = 0.59); 21 (60%) and 18 (51%) patients were symptomatic at baseline and PIPAC3, respectively (p = 0.873). Median OS in the pp cohort was 22.00 months (19.00–NA) from 1st PIPAC. Conclusion Patients with PM of appendiceal origin had objective treatment response after PIPAC and encouraging survival curves call for further prospective evaluation.
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