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Paroxysmal Nocturnal Hemoglobinuria | Practical Perspectives: Investigators Discuss the Current Management of Paroxysmal Nocturnal Hemoglobinuria
Manage episode 453662534 series 1464173
Featuring perspectives from Dr Gloria Gerber, Dr Jamie Koprivnikar, Prof Alexander Röth and Dr Jamile M Shammo, including the following topics:
Introduction: Paroxysmal Nocturnal Hemoglobinuria (PNH) and the General Medical Oncologist
- Diagnosis of and myths and misperceptions about PNH (0:00)
Overview — Biology and Pathophysiology
- Role of complement activation in PNH; classification and clinical presentation (7:00)
- PNH treatments and their complement targets (21:37)
Current Management Approaches
- Mechanistic similarities and differences between crovalimab and other available C5 inhibitors; potential practical advantages of crovalimab (24:56)
- Timing for initiation of treatment for PNH (32:08)
- Management of clinically significant extravascular hemolysis and residual anemia in patients with PNH receiving C5 inhibitor therapy (43:08)
- Risk of evolution to aplastic anemia or myeloid malignancy (45:54)
- Clinical trial database establishing the efficacy and safety of the C5 complement inhibitors eculizumab and ravulizumab for PNH (48:47)
- Activity and safety of and clinical experience with crovalimab (53:03)
- Monitoring and management of PNH in pregnant patients (58:37)
Case Presentations
- Case: A woman in her early 30s who receives a new diagnosis of classical PNH with symptomatic anemia — Dr Gerber (1:03:44)
- Case: A man in his early 30s with PNH initially treated with eculizumab who is transitioned to ravulizumab — Dr Koprivnikar (1:17:32)
- Case: A woman in her early 50s with a remote history of aplastic anemia — Dr Gerber (1:32:24)
- Case: A woman in her late 20s with PNH receiving active C5 inhibitor therapy who wishes to discuss alternative treatment options — Dr Koprivnikar (1:38:00)
1490 episoder
Manage episode 453662534 series 1464173
Featuring perspectives from Dr Gloria Gerber, Dr Jamie Koprivnikar, Prof Alexander Röth and Dr Jamile M Shammo, including the following topics:
Introduction: Paroxysmal Nocturnal Hemoglobinuria (PNH) and the General Medical Oncologist
- Diagnosis of and myths and misperceptions about PNH (0:00)
Overview — Biology and Pathophysiology
- Role of complement activation in PNH; classification and clinical presentation (7:00)
- PNH treatments and their complement targets (21:37)
Current Management Approaches
- Mechanistic similarities and differences between crovalimab and other available C5 inhibitors; potential practical advantages of crovalimab (24:56)
- Timing for initiation of treatment for PNH (32:08)
- Management of clinically significant extravascular hemolysis and residual anemia in patients with PNH receiving C5 inhibitor therapy (43:08)
- Risk of evolution to aplastic anemia or myeloid malignancy (45:54)
- Clinical trial database establishing the efficacy and safety of the C5 complement inhibitors eculizumab and ravulizumab for PNH (48:47)
- Activity and safety of and clinical experience with crovalimab (53:03)
- Monitoring and management of PNH in pregnant patients (58:37)
Case Presentations
- Case: A woman in her early 30s who receives a new diagnosis of classical PNH with symptomatic anemia — Dr Gerber (1:03:44)
- Case: A man in his early 30s with PNH initially treated with eculizumab who is transitioned to ravulizumab — Dr Koprivnikar (1:17:32)
- Case: A woman in her early 50s with a remote history of aplastic anemia — Dr Gerber (1:32:24)
- Case: A woman in her late 20s with PNH receiving active C5 inhibitor therapy who wishes to discuss alternative treatment options — Dr Koprivnikar (1:38:00)
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