Variation in immunoglobulin use and impact on survival in myeloma

Author:

Chai Khai Li1ORCID,Wellard Cameron1,Thao LTP1,Aoki Naomi1,Moore Elizabeth M1ORCID,Augustson Bradley M2,Bapat Akshay3,Blacklock Hilary4,Chng Wee J5,Cooke Rachel6,Forsyth Cecily J7,Goh Yeow‐Tee8,Hamad Nada91011ORCID,Harrison Simon J12,Ho P Joy13ORCID,Hocking Jay14,Kerridge Ian15ORCID,Kim Jin Seok16ORCID,Kim Kihyun17ORCID,King Tracy13,McCaughan Georgia J910ORCID,Mollee Peter18,Morrissey C Orla19,Murphy Nick3,Quach Hang2021,Tan Xuan Ni2,Tso Allison CY22ORCID,Wong Kimberly SQ14,Yoon Sung‐Soo23ORCID,Spencer Andrew24ORCID,Wood Erica M125,McQuilten Zoe K12425

Affiliation:

1. Transfusion Research Unit School of Public Health and Preventive Medicine Monash University Melbourne Australia

2. Department of Haematology Sir Charles Gairdner Hospital Perth Australia

3. Department of Haematology Royal Hobart Hospital Hobart Australia

4. Department of Haematology Middlemore Hospital Auckland New Zealand

5. Department of Haematology‐Oncology and Cancer Science Institute of Singapore National University Cancer Institute Singapore Singapore

6. Department of Haematology Northern Hospital Melbourne Australia

7. Central Coast Haematology North Gosford NSW Gosford Australia

8. Department of Haematology Singapore General Hospital Singapore Singapore

9. Department of Haematology St Vincent's Hospital Sydney Sydney Australia

10. St Vincent's Clinical School University of New South Wales Sydney Australia

11. School of Medicine University of Notre Dame Sydney Australia

12. Department of Haematology Peter MacCallum Cancer Centre and the Royal Melbourne Hospital Melbourne Australia

13. Department of Haematology Royal Prince Alfred Hospital Sydney Australia

14. Department of Haematology Box Hill Hospital Melbourne Australia

15. Department of Haematology Royal North Shore Hospital Sydney Australia

16. Department of Internal Medicine Division of Haematology Yonsei University College of Medicine Severance Hospital Seoul South Korea

17. Department of Medicine Division of Haematology‐Oncology Sungkyunkwan University School of Medicine Samsung Medical Center Seoul South Korea

18. Department of Haematology Princess Alexandra Hospital Brisbane Australia

19. Department of Infectious Diseases The Alfred Hospital and Monash University Melbourne Australia

20. Department of Haematology St Vincent's Hospital Melbourne Melbourne Australia

21. Medicine, Dentistry and Health Sciences The University of Melbourne Melbourne Australia

22. Department of Haematology Tan Tock Seng Hospital Singapore Singapore

23. Division of Haematology/Medical Oncology Seoul National University Hospital Seoul South Korea

24. Department of Haematology The Alfred Hospital Melbourne Australia

25. Department of Haematology Monash Health Melbourne Australia

Abstract

AbstractSerious infection is common in patients with multiple myeloma due to immune deficiency from the underlying disease and/or its treatment. Immunoglobulin replacement is one approach to reduce infection risk in these patients. However, few real‐world data exist on its use in patients with myeloma. We investigated immunoglobulin use in Australia, New Zealand and Asia‐Pacific using registry data and explored its association with survival outcomes. A total of 2374 patients with a median follow‐up time of 29.5 months (interquartile range 13.3–54.3 months) were included in the analysis – 1673 from Australia, 313 Korea, 281 New Zealand and 107 Singapore. Overall, 7.1% of participants received immunoglobulin replacement within 24 months of diagnosis. Patients who received immunoglobulin replacement were likely to be younger, had lower baseline IgG levels (excluding paraprotein), were more likely to have baseline hypogammaglobulinaemia, baseline severe hypogammaglobulinaemia and abnormal baseline fluorescent in‐situ hybridisation status, receive first‐line myeloma treatment with immunomodulatory drugs or anti‐CD38 therapy and undergo upfront autologous stem cell transplant. In our patient cohort, the use of immunoglobulin was not associated with overall survival benefit at the time of last follow‐up (adjusted hazard ratio 0.72, 95% CI 0.46–1.14, p = 0.16). Understanding treatment approaches in clinical practice can help support future planning and provision of immunoglobulin resources.

Publisher

Wiley

Reference27 articles.

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