Ann Coloproctol.  2025 Feb;41(1):57-67. 10.3393/ac.2024.00339.0048.

Is clinical complete response as accurate as pathological complete response in patients with mid-low locally advanced rectal cancer?

Affiliations
  • 1Department of Surgery, Bogazici Academy for Clinical Sciences, Istanbul, Turkiye
  • 2Department of General Surgery, Alibey Hospital, Istanbul, Turkiye
  • 3Department of Colorectal Surgery, Portsmouth Hospitals University NHS Trust, Portsmouth, UK
  • 4Department of Radiology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkiye
  • 5Department of Pathology, Maslak Acıbadem Hospital, Istanbul, Turkiye

Abstract

Purpose
The standard treatment for locally advanced rectal cancer involves neoadjuvant chemoradiation followed by total mesorectal excision surgery. A subset of patients achieves pathologic complete response (pCR), representing the optimal treatment outcome. This study compares the long-term oncological outcomes of patients who achieved pCR with those who attained clinical complete response (cCR) after total neoadjuvant therapy, managed using a watch-and-wait approach.
Methods
This study retrospectively evaluated patients with mid-low locally advanced rectal cancer who underwent neoadjuvant treatment from January 1, 2005, to May 1, 2023. The pCR and cCR groups were compared based on demographic, clinical, histopathological, and long-term survival outcomes.
Results
The median follow-up times were 54 months (range, 7–83 months) for the cCR group (n=73), 96 months (range, 7–215 months) for the pCR group (n=63), and 72 months (range, 4–212 months) for the pathological incomplete clinical response (pICR) group (n=627). In the cCR group, 15 patients (20.5%) experienced local regrowth, and 5 (6.8%) developed distant metastasis (DM). The pCR group had no cases of local recurrence, but 3 patients (4.8%) developed DM. Among the pICR patients, 58 (9.2%) experienced local recurrence, and 92 (14.6%) had DM. Five-year disease-free survival rates were 90.0% for cCR, 92.0% for pCR, and 69.5% for pICR (P=0.022). Five-year overall survival rates were 93.1% for cCR, 92.0% for pCR, and 78.1% for pICR. There were no significant differences in outcomes between the cCR and pCR groups (P=0.810); however, the pICR group exhibited poorer outcomes (P=0.002).
Conclusion
This study shows no significant long-term oncological differences between patients who exhibited cCR and those who experienced pCR.

Keyword

Rectal cancer; Local advanced rectal cancer; Clinical complete response; Pathological complete response; Neoadjuvant therapy
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