4.3 Article

Preoperative systemic chemotherapy alters the histopathological growth patterns of colorectal liver metastases

Journal

JOURNAL OF PATHOLOGY CLINICAL RESEARCH
Volume 8, Issue 1, Pages 48-64

Publisher

WILEY
DOI: 10.1002/cjp2.235

Keywords

colorectal cancer; colorectal liver metastases; histopathological growth patterns; systemic chemotherapy

Categories

Funding

  1. Swedish Cancer Society (Sweden)
  2. Cancer Research UK (United Kingdom)
  3. Ligue Nationale Contre le Cancer (France)
  4. National Cancer Institute (Bethesda, MD, USA) [5U10-CA11488-28, 5U10 CA11488-37]

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This study investigated the impact of preoperative systemic chemotherapy on tumor growth patterns, revealing a significant increase in the presence of desmoplastic HGP in CRLM patients prior to treatment. This change was consistently associated across different cohorts.
Histopathological growth patterns (HGPs) are a reliable, reproducible, and strong prognostic biomarker that can be assessed on haematoxylin and eosin-stained sections of resected colorectal liver metastases (CRLM). Assessment estimates the relative fraction of the tumour-liver interface for each of the three growth patterns; the desmoplastic HGP reflects good prognosis. Whether preoperative chemotherapy affects the HGP is currently unclear. The present international multicentre study evaluates this in an original cohort of 877 consecutive patients treated in the Netherlands, an external validation cohort of 1,203 consecutive patients treated in the USA, and a post hoc analysis from the phase III randomised controlled European Organization for Research and Treatment of Cancer (EORTC) 40983 trial (n = 70). All patients underwent resection of CRLM with or without preoperative systemic chemotherapy. Trial patients were randomised between perioperative chemotherapy and resection or resection alone. HGPs were determined according to consensus guidelines and compared for preoperative treatment status. Data from three separate tumour regression grading systems were available for the trial cohort. These were correlated with HGP stratified for treatment arm. In the original cohort, the average presence of desmoplastic HGP was 43% for chemo-naive versus 67% for preoperatively treated patients (p < 0.001). A significant association between chemotherapy and desmoplastic HGP was found on multivariable analysis (beta [95% confidence interval, [CI]: 24.57 [18.28-30.87], p < 0.001). In the validation cohort, the average presence of desmoplastic HGP was 40% for chemo-naive versus 63% for preoperatively treated patients (p < 0.001). This association remained on multivariable analysis (beta [95% CI]: 24.18 [18.70-29.66], p < 0.001). In the EORTC 40983 trial, the average desmoplastic HGP presence was 33% in the resection arm versus 61% in the chemotherapy arm (p = 0.005). Chemotherapy was independently associated with an increase in desmoplastic HGP (beta [95% CI]: 23.29 [1.78-44.79], p = 0.022). All three tumour regression gradings were significantly associated with the desmoplastic HGP in the chemotherapy arm (all p < 0.04). None were associated in the resection arm (all p > 0.11). Preoperative chemotherapy induces histopathological changes that alter the HGP of CRLM.

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