Background
In patients with resectable colorectal liver metastases (CRLM), distinct histopathological growth patterns (HGPs) develop at the interface between the tumour and surrounding tissue. The desmoplastic (d) HGP is characterised by angiogenesis and a peripheral fibrotic rim, whereas non-angiogenic HGPs co-opt endogenous sinusoidal hepatic vasculature. Evidence from previous studies has suggested that patients with dHGP in their CRLM have improved prognosis as compared to patients with non-desmoplastic HGPs. However, these studies were relatively small and applied arbitrary cut-off values for the determination of the predominant HGP. We have now investigated the prognostic effect of dHGP in a large cohort of patients with CRLM resected either with or without neoadjuvant chemotherapy.
Methods
All consecutive patients undergoing a first partial hepatectomy for CRLM between 2000 and 2015 at a tertiary referral centre were considered for inclusion. HGPs were assessed in archival H&E stained slides according to recently published international consensus guidelines. The dHGP was defined as desmoplastic growth being present in 100% of the interface between the tumour and surrounding liver.
Results
In total, HGPs in CRLMs from 732 patients were assessed. In the chemo-naive patient cohort (
n
= 367), the dHGP was present in 19% (
n
= 68) and the non-dHGP was present in 81% (
n
= 299) of patients. This dHGP subgroup was independently associated with good overall survival (OS) (HR: 0.39,
p
< 0.001) and progression-free survival (PFS) (HR: 0.54,
p
= 0.001). All patients with any CRLM with a non-dHGP had significantly reduced OS compared to those patients with 100% dHGP, regardless of the proportion of non-dHGP (all
p
values ≤ 0.001). In the neoadjuvantly treated patient cohort (
n
= 365), more patients were found to express dHGP (
n
= 109, 30%) (adjusted odds ratio: 2.71,
p
< 0.001). On univariable analysis, dHGP was associated with better OS (HR 0.66,
p
= 0.009) and PFS (HR 0.67,
p
= 0.002). However, after correction for confounding by means of multivariable analysis no significant association of dHGP with OS (HR 0.92,
p
= 0.623) or PFS (HR 0.76,
p
= 0.065) was seen.
Conclusions
The current study demonstrates that the angiogenic dHGP in CRLM resected from chemo-naive patients acts as a strong, positive prognostic marker, unmatched by any other prognosticator. This observation warrants the evaluation of the clinical utility of HGPs in prospective clinical trials.
Electronic supplementary material
The online version of this article (10.1007/s1045...
Background
After resection of colorectal cancer liver metastases (CRLM) two main histopathological growth patterns can be observed; a desmoplastic and a non-desmoplastic subtype. The desmoplastic subtype has been associated with superior survival. These findings require external validation.
Methods
An international multicenter retrospective cohort study was conducted in patients treated surgically for CRLM at three tertiary hospitals in the US and the Netherlands. Determination of histopathological growth patterns was performed on hematoxylin & eosin stained sections of resected CRLM according to international guidelines. Patients displaying a desmoplastic histopathological phenotype (only desmoplastic growth observed) were compared to patients with a non-desmoplastic phenotype (any non-desmoplastic growth observed). Cut-off analyses on the extent of non-desmoplastic growth were performed. Overall (OS) and disease-free (DFS) survival were estimated using Kaplan-Meier and multivariable Cox analysis. All statistical tests were 2-sided.
Results
In total 780 patients were eligible. A desmoplastic phenotype was observed in 19.1% and was associated with microsatellite instability (14.6% versus 3.6%, p = .01). Desmoplastic patients had superior 5-year OS (73.4% [95% CI = 64.1–84.0] versus 44.2% [95% CI = 38.9–50.2], p < .001) and DFS (32.0% [95% CI = 22.9–44.7] versus 14.7% [95% CI = 11.7–18.6], p < .001) compared to their non-desmoplastic counterparts. A desmoplastic phenotype was associated with an adjusted hazard ratio for death of 0.36 (95% CI = 0.23–0.58), and 0.50 (95% CI = 0.37–0.66) for cancer recurrence. Prognosis was independent of KRAS and BRAF status. The cut-off analyses found no prognostic relationship between either OS or DFS and the extent of non-desmoplastic growth observed (all p > .1).
Conclusions
This external validation study confirms the remarkably good prognosis after surgery for CRLM in patients with a desmoplastic phenotype. The extent of non-desmoplastic growth does not impact prognosis.
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