The role of infiltrating lymphocytes in the neo-adjuvant treatment of women with HER2-positive breast cancer.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Jun 2021
Historique:
received: 16 05 2020
accepted: 22 04 2021
pubmed: 14 5 2021
medline: 24 6 2021
entrez: 13 5 2021
Statut: ppublish

Résumé

Pre-treatment tumour-associated lymphocytes (TILs) and stromal lymphocytes (SLs) are independent predictive markers of future pathological complete response (pCR) in HER2-positive breast cancer. Whilst studies have correlated baseline lymphocyte levels with subsequent pCR, few have studied the impact of neoadjuvant therapy on the immune environment. We performed TIL analysis and T-cell analysis by IHC on the pretreatment and 'On-treatment' samples from patients recruited on the Phase-II TCHL (NCT01485926) clinical trial. Data were analysed using the Wilcoxon signed-rank test and the Spearman rank correlation. In our sample cohort (n = 66), patients who achieved a pCR at surgery, post-chemotherapy, had significantly higher counts of TILs (p = 0.05) but not SLs (p = 0.08) in their pre-treatment tumour samples. Patients who achieved a subsequent pCR after completing neo-adjuvant chemotherapy had significantly higher SLs (p = 9.09 × 10 The immune system may be 'primed' prior to neoadjuvant treatment in those patients who subsequently achieve a pCR. In those patients who achieve a pCR, their immune response may return to baseline after only 1 cycle of treatment. However, in those who did not achieve a pCR, neo-adjuvant treatment may stimulate lymphocyte influx into the tumour.

Sections du résumé

BACKGROUND BACKGROUND
Pre-treatment tumour-associated lymphocytes (TILs) and stromal lymphocytes (SLs) are independent predictive markers of future pathological complete response (pCR) in HER2-positive breast cancer. Whilst studies have correlated baseline lymphocyte levels with subsequent pCR, few have studied the impact of neoadjuvant therapy on the immune environment.
METHODS METHODS
We performed TIL analysis and T-cell analysis by IHC on the pretreatment and 'On-treatment' samples from patients recruited on the Phase-II TCHL (NCT01485926) clinical trial. Data were analysed using the Wilcoxon signed-rank test and the Spearman rank correlation.
RESULTS RESULTS
In our sample cohort (n = 66), patients who achieved a pCR at surgery, post-chemotherapy, had significantly higher counts of TILs (p = 0.05) but not SLs (p = 0.08) in their pre-treatment tumour samples. Patients who achieved a subsequent pCR after completing neo-adjuvant chemotherapy had significantly higher SLs (p = 9.09 × 10
CONCLUSIONS CONCLUSIONS
The immune system may be 'primed' prior to neoadjuvant treatment in those patients who subsequently achieve a pCR. In those patients who achieve a pCR, their immune response may return to baseline after only 1 cycle of treatment. However, in those who did not achieve a pCR, neo-adjuvant treatment may stimulate lymphocyte influx into the tumour.

Identifiants

pubmed: 33983492
doi: 10.1007/s10549-021-06244-1
pii: 10.1007/s10549-021-06244-1
pmc: PMC8197702
doi:

Substances chimiques

Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

635-645

Subventions

Organisme : Irish Cancer Society
ID : CCRC13GAL

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Auteurs

A J Eustace (AJ)

National Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland. alex.eustace@dcu.ie.

S F Madden (SF)

Data Science Centre, Royal College of Surgeons in Ireland, Dublin, Ireland.

J Fay (J)

Department of Histopathology, Royal College of Surgeons in Ireland, Dublin, Ireland.

D M Collins (DM)

National Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.

E W Kay (EW)

Department of Histopathology, Royal College of Surgeons in Ireland, Dublin, Ireland.

K M Sheehan (KM)

Department of Histopathology, Royal College of Surgeons in Ireland, Dublin, Ireland.
Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.

S Furney (S)

Department of Physiology, Royal College of Surgeons in Ireland, Dublin, Ireland.

B Moran (B)

Conway Institute, University College Dublin, Dublin, Ireland.

A Fagan (A)

Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.

P G Morris (PG)

Department of Medical Oncology, Beaumont Hospital, Dublin, Ireland.

A Teiserskiene (A)

Cancer Trials Ireland, Dublin, Ireland.

A D Hill (AD)

Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.

L Grogan (L)

Department of Medical Oncology, Beaumont Hospital, Dublin, Ireland.

J M Walshe (JM)

Department of Medical Oncology, St Vincent's University Hospital, Dublin, Ireland.

O Breathnach (O)

Department of Medical Oncology, Beaumont Hospital, Dublin, Ireland.

C Power (C)

Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.

D Duke (D)

Department of Radiology, Beaumont Hospital, Dublin, Ireland.

K Egan (K)

Cancer Clinical Trials and Research Unit, Beaumont Hospital, Dublin, Ireland.

W M Gallagher (WM)

Conway Institute, University College Dublin, Dublin, Ireland.

N O'Donovan (N)

National Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.

J Crown (J)

National Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
Cancer Trials Ireland, Dublin, Ireland.

S Toomey (S)

Medical Oncology Group, Department of Molecular Medicine, Royal College of Surgeons in Ireland, Dublin, Ireland.

B T Hennessy (BT)

Cancer Trials Ireland, Dublin, Ireland.
Medical Oncology Group, Department of Molecular Medicine, Royal College of Surgeons in Ireland, Dublin, Ireland.

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Classifications MeSH