Predictive and prognostic effect of ABO blood group on immune checkpoint inhibitors

Author:

Ergun Yakup1,Esen Selin Akturk2,Bardakci Murat2,Ucar Gokhan2,Kalkan Ziya3,Urakci Zuhat3,Seyran Erdogan4,Dogan Mutlu4,Eren Tulay5,Aslan Volkan6,Kahraman Seda2,Genc Emine Eylem7,Acikgoz Yusuf2,Dirikoc Merve2,Esen Irfan8,Uncu Dogan2

Affiliation:

1. Department of Medical Oncology, Batman Training and Research Hospital, Batman, Turkey

2. Department of Medical Oncology, University of Health Sciences Ankara City Hospital, Ankara, Turkey

3. Department of Medical Oncology, Dicle University Faculty of Medicine, Diyarbakır, Turkey

4. Department of Medical Oncology, UHS Dr Abdurrahman Yurtaslan Oncology Training and Research Hospital, Ankara, Turkey

5. Department of Medical Oncology, UHS Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey

6. Department of Medical Oncology, Gazi University Faculty of Medicine, Ankara, Turkey

7. Department of Hematology, Batman Training and Research Hospital, Batman, Turkey

8. Department of Internal Medicine, VM Medical Park (Kecioren) Hospital, Ankara, Turkey

Abstract

BACKGROUND: The relationship of the ABO blood group system with the immune response is known, but its relationship with immune checkpoint inhibitors (ICIs) has not been clearly investigated until now. OBJECTIVE: In this study, the relationship between different blood groups and nivolumab treatment response in patients with advanced malignant melanoma was investigated. METHODS: The data of patients who used nivolumab for advanced malignant melanoma between April 2018 and April 2021 were retrospectively reviewed. RESULTS: A total of 73 patients were included in the study. In the progression-free survival (PFS) analysis according to blood groups, it was 3.9 months, 16.1 months, 20.0 months and 3.0 months for A, B, AB and O, respectively (p= 0.1). Overall survival (OS) analysis according to blood groups was 5.1 months, 25.0 months, 20.0 months and 9.3 months for A, B, AB and O, respectively (p= 0.1). The B antigen group (B or AB) had significantly longer PFS and OS than the non-B antigen group (A or O) (16.1 vs. 3.5 months for PFS, respectively, p= 0.03; 20.0 vs. 7.4 months for OS, respectively, p= 0.02). CONCLUSIONS: The presence of B antigen provides a significant advantage in terms of survival in patients using ICIs for advanced melanoma.

Publisher

IOS Press

Subject

Cancer Research,Genetics,Oncology,General Medicine

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