Abstract
Liver is the third most common organ for breast cancer (BC) metastasis. Two main histopathological growth patterns (HGP) exist in liver metastases (LM): desmoplastic and replacement. Although a reduced immunotherapy efficacy is reported in patients with LM, tumor-infiltrating lymphocytes (TIL) have not yet been investigated in BCLM. Here, we evaluate the distribution of the HGP and TIL in BCLM, and their association with clinicopathological variables and survival. We collect samples from surgically resected BCLM (n = 133 patients, 568 H&E sections) and post-mortem derived BCLM (n = 23 patients, 97 H&E sections). HGP is assessed as the proportion of tumor liver interface and categorized as pure-replacement ('pure r-HGP') or any-desmoplastic ('any d-HGP'). We score the TIL according to LM-specific guidelines. Associations with progression-free (PFS) and overall survival (OS) are assessed using Cox regressions. We observe a higher prevalence of 'any d-HGP' (56%) in the surgical samples and a higher prevalence of 'pure r-HGP' (83%) in the post-mortem samples. In the surgical cohort, no evidence of the association between HGP and clinicopathological characteristics is observed except with the laterality of the primary tumor (p value = 0.049) and the systemic preoperative treatment before liver surgery (p value = .039). TIL is less prevalent in 'pure r-HGP' as compared to 'any d-HGP' (p value = 0.001). 'Pure r-HGP' predicts worse PFS (HR: 2.65; CI: (1.45-4.82); p value = 0.001) and OS (HR: 3.10; CI: (1.29-7.46); p value = 0.011) in the multivariable analyses. To conclude, we demonstrate that BCLM with a 'pure r-HGP' is associated with less TIL and with the worse outcome when compared with BCLM with 'any d-HGP'. These findings suggest that HGP could be considered to refine treatment approaches.
| Original language | English |
|---|---|
| Article number | 100 |
| Pages (from-to) | 1-11 |
| Number of pages | 11 |
| Journal | NPJ Breast Cancer |
| Volume | 9 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Dec 2023 |
| Externally published | Yes |
Bibliographical note
Funding Information:The authors thank the patients and their families and the Biobanks from all participating hospitals. This work has been supported by the “Fondation contre le cancer” (C/2020/1441). M.D.S. is funded by the KU Leuven Fund Nadine de Beauffort. T.G. and F.R. are funded by FWO through a research fellowship. G.F. is the recipient of a post-doctoral mandate from the KOOR of the UH-Leuven. Finally, K.V.B. is funded by the KU Leuven Fund Nadine de Beaufort and a Conquer Cancer—Lobular Breast Cancer Alliance Young Investigator Award for Invasive Lobular Carcinoma Research, supported by the Lobular Breast Cancer Alliance. M.G. has been supported by the Swedish Research Council (project nr. 2018-02023), J.E. by Region Stockholm and the Bengt Ihre Foundation, and CMF by The Swedish Society for Medical Research (PD21-0114).
Funding Information:
The authors thank the patients and their families and the Biobanks from all participating hospitals. This work has been supported by the “Fondation contre le cancer” (C/2020/1441). M.D.S. is funded by the KU Leuven Fund Nadine de Beauffort. T.G. and F.R. are funded by FWO through a research fellowship. G.F. is the recipient of a post-doctoral mandate from the KOOR of the UH-Leuven. Finally, K.V.B. is funded by the KU Leuven Fund Nadine de Beaufort and a Conquer Cancer—Lobular Breast Cancer Alliance Young Investigator Award for Invasive Lobular Carcinoma Research, supported by the Lobular Breast Cancer Alliance. M.G. has been supported by the Swedish Research Council (project nr. 2018-02023), J.E. by Region Stockholm and the Bengt Ihre Foundation, and CMF by The Swedish Society for Medical Research (PD21-0114).
Publisher Copyright:
© 2023, The Author(s).
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