A virtual roundtable discussion with noted investigators Prof
Meletios A Dimopoulos and Dr Steven P Treon for a review of recent
innovations in the treatment of Waldenström Macroglobulinemia.
Pathophysiology, symptoms and common genetic mutations
associated with Waldenström macroglobulinemia (WM) (00:00)
Somatic mutations in MYD88 (L265P) and CXCR4 and implications
for prognosis and therapy (1:46)
Diagnostic criteria for WM (7:12)
Case (Dr Treon): A man in his late 60s with WM
experiences an IgM flare and worsening peripheral neuropathy during
first-line treatment with rituximab (8:55)
Indications for the initiation of therapy for patients with WM
(12:02)
Management approach for patients with WM experiencing IgM flare
after treatment with rituximab (13:40)
Activity of the Bruton tyrosine kinase (BTK) inhibitor
ibrutinib alone or in combination with rituximab in patients with
WM (15:35)
Perspective on the use of ibrutinib with or without rituximab
as front-line therapy for WM (17:51)
Symptoms and management of hyperviscosity syndrome associated
with WM (21:07)
Role of obinutuzumab in the management of WM (23:58)
Case (Prof Dimopoulos): A man in his early 50s
with WM and a MYD88 L265P mutation attains a very good partial
response to first-line therapy with
bortezomib/dexamethasone/rituximab (25:24)
Selection of therapy for patients with WM in the first-line
setting (27:50)
Efficacy and tolerability of proteasome inhibitors for WM
(31:42)
Peripheral neuropathy associated with WM and implications for
therapy (34:39)
Duration of ibrutinib therapy for WM and impact of treatment
holidays (37:27)
Side effects associated with ibrutinib; monitoring and
management of atrial fibrillation (39:44)
Case (Dr Treon): A woman in her mid-60s
diagnosed with WM and a MYD88 L265P mutation experiences a dramatic
response after receiving ibrutinib as first-line therapy
(44:44)
Response and tolerability with ibrutinib in the front-line
setting (46:56)
Case (Prof Dimopoulos): A woman in her early
80s with a history of hypertension and atrial fibrillation is
diagnosed with WM with a MYD88 L265P mutation and receives
ibrutinib and anticoagulation therapy (49:39)
Perspective on the use of ibrutinib for elderly patients and
those with a history of atrial fibrillation (51:37)
Activity of the BTK inhibitor zanubrutinib in patients with WM
(54:36)
Results of the Phase III iNNOVATE trial evaluating ibrutinib
with rituximab versus rituximab alone for patients with previously
untreated or relapsed/refractory WM (56:19)
Ongoing investigation of CXCR4 inhibitors and the Bcl-2
inhibitor venetoclax for WM (57:59)
Biologic rationale and role for venetoclax in WM (1:00:28)
Tumor lysis syndrome associated with venetoclax
(1:04:11)
Novel agents and approaches under investigation for WM
(1:05:26)
Therapeutic options for patients with WM after disease
progression on ibrutinib (1:06:56)
Featuring the video recorded proceedings of events held in conjunction with important scientific symposia, live webcasts and closed meetings featuring the perspectives of renowned clinical investigators, these videos provide an overview of important advances in the management of a number of solid tumors and hematologic cancers.