Published in:
26-08-2023 | Cytostatic Therapy | Peritoneal Surface Malignancy
Patterns of Recurrence in Appendix Cancer After Complete Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy
Authors:
Andrei Nikiforchin, MD, Armando Sardi, MD, FACS, Mary Caitlin King, BS, Ekaterina Baron, MD, Felipe Lopez-Ramirez, MD, Luis Felipe Falla-Zuniga, MD, Philipp Barakat, MD, Sergei Iugai, MD, Kathleen Pawlikowski, BA, Carol Nieroda, MD, Vadim Gushchin, MD, FACS
Published in:
Annals of Surgical Oncology
|
Issue 12/2023
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Abstract
Background
It is thought that low-grade (LG) appendiceal cancer (AC) demonstrates predominantly intraperitoneal recurrence (IPR) after cytoreductive surgery with hyperthermic intraperitoneal chemotherapy (CRS/HIPEC), whereas high-grade (HG) tumors progress both intra- and extraperitoneally (EPR). However, evidence supporting this conception is lacking; therefore, we assessed recurrence in various AC histologies.
Methods
A retrospective, cohort study was conducted by using a single-center database (1998–2022). Recurrence patterns (IPR, EPR, combined) were identified for LG, HG, high-grade with signet ring cells (SRC), and goblet cell carcinoma (GCC).
Results
We included 432 complete (CC-0/1) CRS/HIPECs: 200 LG, 114 HG, 72 SRC, and 46 GCC. Median follow-up was 78 (95% confidence interval [CI] 70–86) months. Overall, 34% (n = 148) of patients recurred. IPR was the most common (LG 16%, HG 27%, SRC 36%, GCC 26%) with median time to recurrence (MTR) of 21 (IQR: 12–40) months. EPR (liver, lung, pleura, lymph nodes, or bones) occurred in LG 3%, HG 9%, SRC 22%, and GCC 7%. MTR was 11 (IQR: 4–16) months. Combined pattern occurred in LG 0%, HG 8%, SRC 7%, and GCC 0%. MTR was 13 (IQR: 7–18) months. Iterative surgery was performed in 53% IPR, 18% EPR, and 51% combined. Median post-recurrence survival was longer after IPR compared with EPR and combined recurrence: 36 (95% CI 25–47) versus 13 (95% CI 7–19) and 18 (95% CI 6–30) months (p < 0.01).
Conclusions
After complete CRS/HIPEC, IPR was the predominant pattern in all AC histologies and occurred later. Post-recurrence survival after IPR was longer. Knowing AC recurrence patterns can help to understand its biology and plan follow-up and post-relapse management.