Pregled bibliografske jedinice broj: 1104005
Prognostic value of compartmental spatial analysis of tumour: Infiltrating lymphocytes in triple-negative breast cancer
Prognostic value of compartmental spatial analysis of tumour: Infiltrating lymphocytes in triple-negative breast cancer // Meeting Abstract. U: Annals of oncology 31(suppl.4)
Madrid, Španjolska, 2020. str. 285-285 doi:10.1016/j.annonc.2020.08.231 (poster, međunarodna recenzija, prošireni sažetak, ostalo)
CROSBI ID: 1104005 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Prognostic value of compartmental spatial
analysis of tumour: Infiltrating lymphocytes in
triple-negative breast cancer
Autori
Tečić Vuger, Ana ; Šeparović, Robert ; Vazdar, Ljubica ; Pavlović, Mirjana ; Šitić, Sandra ; Lovasić Belac, Ingrid Belac ; Vrbanec, Damir
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, prošireni sažetak, ostalo
Izvornik
Meeting Abstract. U: Annals of oncology 31(suppl.4)
/ - , 2020, 285-285
Skup
ESMO Virtual Congress 2020
Mjesto i datum
Madrid, Španjolska, 19.09.2020. - 18.10.2020
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Infiltrating lymphocytes ; triple-negative breast cancer
Sažetak
Background: Analyses reported to date on tumour infiltrating lymphocytes (TIL) have evaluated mostly stromal, possibly intratumoral TIL, but we have not found any in which TIL were evaluated spatially, by stromal and intratumoral category, separately in compartments of central tumour (CT) and invasive margin (IM). Methods: We retrospectively analysed consecutive sample of 152 early TNBC patients treated at our institution 2009-2012. TIL were assessed by HE, using standard FFPE samples, according to International Working Group for Evaluation of TIL recommendation, both stromal TIL (sTIL) and intratumoral TIL (iTIL), spatially, in compartments of CT and IM. Results: Spatial analysis revealed the following: overall sTIL content was in median 19%, iTIL 5%, TIL in CT 5%, at IM 18%, sTIL in CT 5%, iTIL in CT 1%, sTIL at IM 30%, and iTIL at IM 5%. Prevalence of intermediate or high TIL content, defined as 10% wassTIL in CT in 48%, iTIL in CT in 23%, sTIL at IM in 86%, and iTIL at IM in 47% of cases. Quarter of patients had TIL>50% in any of the evaluated compartments. There was statistically significant correlation between sTIL and iTIL, presence of TIL in all four evaluated compartments, and correlation was stronger among sTIL and iTIL in CT, and sTIL and iTIL at IM, than between the two compartments. In bivariable analysis all TIL indicators were significantly associated with longer DFS and OS. Overall, patients with TIL10% in all four evaluated compartments (sTIL and iTIL, in CT and IM) were shown to have statistically significantly better DFS and OS, compared to those with TIL<10%. After adjustment for potential confounders using Cox proportional hazard regression, significant predictors of OS were sTIL (p0.007), iTIL if present in 10% (p0.022), TIL at IM (p0.002), sTIL at IM (p0.001), and iTIL at IM if present in 10% (p0.036). Conclusions: Compartmental morphological analysis of TIL reveals frequent intermediate to high density of TIL content on IM and their overall statistically significant prognostic impact. This draws attention to this neglected tumoral compartment and directs the question towards the different biology, cell composition, and role of each tumour morphological compartment, a phenomenon that should definitely be further explored. Legal entity responsible for the study: The authors
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinika za tumore,
Klinički bolnički centar Rijeka,
Sveučilište Jurja Dobrile u Puli
Profili:
Ingrid Belac-Lovasić
(autor)
Ljubica Vazdar
(autor)
Robert Šeparović
(autor)
Mirjana Pavlović
(autor)
Damir Vrbanec
(autor)
Ana Tečić Vuger
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE