Efficacy and safety of cyclosporine A treatment in autoimmune cytopenias: the experience of two Italian reference centers. (May 2022)
- Record Type:
- Journal Article
- Title:
- Efficacy and safety of cyclosporine A treatment in autoimmune cytopenias: the experience of two Italian reference centers. (May 2022)
- Main Title:
- Efficacy and safety of cyclosporine A treatment in autoimmune cytopenias: the experience of two Italian reference centers
- Authors:
- Fattizzo, Bruno
Cantoni, Silvia
Giannotta, Juri Alessandro
Bandiera, Laura
Zavaglia, Rachele
Bortolotti, Marta
Barcellini, Wilma - Abstract:
- Background: Immune thrombocytopenia (ITP) and autoimmune hemolytic anemia (AIHA) show good responses to frontline steroids. About two-third of cases relapse and require second-line treatment, including rituximab, mainly effective in AIHA, and thrombopoietin-receptor agonists (TPO-RAs) in ITP, while the use of splenectomy progressively decreased due to concerns for infectious/thrombotic complications. For those failing second line, immunosuppressants may be considered. Objectives: The aim of this study was to evaluate the efficacy of cyclosporine treatment in patients with ITP and AIHA. Design: In this retrospective study, we evaluated the efficacy and safety of cyclosporine A (CyA) in ITP ( N = 29) and AIHA ( N = 10) patients followed at two reference centers in Milan, Italy. Methods: Responses were classified as partial [Hb > 10 or at least 2 g/dl increase from baseline, platelets (PLT) > 30 × 10 9 /l with at least doubling from baseline] and complete (Hb > 12 g/dl or PLT > 100 × 10 9 /l) and evaluated at 3, 6, and 12 months. Treatment emergent adverse events were also registered. Results: The median time from diagnosis to CyA was 35 months (3–293), and patients had required a median of 4 (1–8) previous therapy lines. Median duration of CyA was 28 (2–140) months and responses were achieved in 86% of ITP and 50% of AIHA subjects. Responders could reduce or discontinue concomitant treatment and resolved PLT fluctuations on TPO-RA. CyA was generally well tolerated, and onlyBackground: Immune thrombocytopenia (ITP) and autoimmune hemolytic anemia (AIHA) show good responses to frontline steroids. About two-third of cases relapse and require second-line treatment, including rituximab, mainly effective in AIHA, and thrombopoietin-receptor agonists (TPO-RAs) in ITP, while the use of splenectomy progressively decreased due to concerns for infectious/thrombotic complications. For those failing second line, immunosuppressants may be considered. Objectives: The aim of this study was to evaluate the efficacy of cyclosporine treatment in patients with ITP and AIHA. Design: In this retrospective study, we evaluated the efficacy and safety of cyclosporine A (CyA) in ITP ( N = 29) and AIHA ( N = 10) patients followed at two reference centers in Milan, Italy. Methods: Responses were classified as partial [Hb > 10 or at least 2 g/dl increase from baseline, platelets (PLT) > 30 × 10 9 /l with at least doubling from baseline] and complete (Hb > 12 g/dl or PLT > 100 × 10 9 /l) and evaluated at 3, 6, and 12 months. Treatment emergent adverse events were also registered. Results: The median time from diagnosis to CyA was 35 months (3–293), and patients had required a median of 4 (1–8) previous therapy lines. Median duration of CyA was 28 (2–140) months and responses were achieved in 86% of ITP and 50% of AIHA subjects. Responders could reduce or discontinue concomitant treatment and resolved PLT fluctuations on TPO-RA. CyA was generally well tolerated, and only two serious infectious complications in elderly patients on concomitant steroids suggesting caution in this patient population. Conclusion: CyA may be advisable in ITP, which is not well controlled under TPO-RA, and in AIHA failing rituximab, particularly if ineligible in clinical trial. … (more)
- Is Part Of:
- Therapeutic advances in hematology. Volume 13(2022)
- Journal:
- Therapeutic advances in hematology
- Issue:
- Volume 13(2022)
- Issue Display:
- Volume 13, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 13
- Issue:
- 2022
- Issue Sort Value:
- 2022-0013-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-05
- Subjects:
- autoimmune hemolytic anemia -- cyclosporine A -- Evans syndrome -- immune thrombocytopenia
Hematology -- Periodicals
Hematologic Diseases -- therapy -- Periodicals
Hematology -- Periodicals
616.15005 - Journal URLs:
- http://tah.sagepub.com/ ↗
http://www.uk.sagepub.com ↗ - DOI:
- 10.1177/20406207221097780 ↗
- Languages:
- English
- ISSNs:
- 2040-6207
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24322.xml