HEMATOLOGY

Brian T. Hill, MD, PhD, shares more insight on acalabrutinib and ibrutinib’s efficacy in patients with MCL and highlights emerging novel strategies in the treatment landscape.

C. Ola Landgren, MD, PhD, recently shared the treatment considerations and decisions he makes when treating patients with newly diagnosed multiple myeloma

Enrollment in a phase I/II clinical trial began recently for a study of PT-112 monotherapy in patients with relapsed or refractory multiple myeloma, according a news release from Phosplatin Therapeutics LLC, the company developing the small molecule conjugate.

Combining consolidative radioimmunotherapy and sequential maintenance rituximab following chemoimmunotherapy improved progression-free survival at 3 years in patients with previously untreated follicular lymphoma, according to findings from the phase II SWOG S0801 study recently published in <em>The Lancet Hematology</em>.

Based on findings from a phase I trial presented at the 2017 ASH Annual Meeting, ivosidenib (AG-120) has been granted a priority review designation by the FDA for the&nbsp;treatment of patients with relapsed/refractory <em>IDH1</em>-mutant acute myeloid leukemia.

The clinical course of chronic lymphocytic leukemia is highly variable, and a subset of patients may never need clinical intervention. However, most patients will eventually require treatment during their disease.

Using next-generation squencing methods, researchers are attempting to combine clinical and genomic biomarkers to identify patients with smoldering multiple myeloma who are at high risk for disease progression.

Susan O&rsquo;Brien, MD,&nbsp; discusses the tremendous impact that has been seen with ibrutinib following the long-term follow-up of the RESONATE studies and highlights where this regimen is headed in the future of treatment for patients with CLL.

Based on improved insight into chronic lymphocytic leukemia biology and pathophysiology, approaches to identify patients who are at higher risk for disease progression have been refined, as have strategies to select therapies that maximize treatment outcomes due to their selectivity for distinctive phenotypic or physiological features of the respective CLL cells.

Matthew S. Davids, MD,&nbsp;sheds light on the significant findings of this study and gave a look ahead to ibrutinib combination therapies in the future treatment landscape of CLL.

According to recently published results of the&nbsp;international, double-blind randomized phase III 482 Study&nbsp;in&nbsp;<em>The Lancet Oncology,&nbsp;</em>^&nbsp;denosumab was noninferior to zoledronic acid (Zometa) in preventing skeletal-related event in patients with newly diagnosed multiple myeloma.

Prospects for patients with chronic lymphocytic leukemia have improved with the use of targeted agents such as ibrutinib; however, complete remissions are rare, and treatment options for patients relapsing after treatment with ibrutinib remain limited.

Recent years have seen major advances in diagnostic approaches in CLL, and disease assessment may now include analysis of multiple genetic mutations in addition to recurrent cytogenetic changes. Furthermore, with the development of novel treatment approaches, the significance of prognostic markers is shifting.

Overall survival was extended for patients with relapsed or refractory multiple myeloma by nearly 8 months with the&nbsp;combination of carfilzomib, lenalidomide, and dexamethasone compared with&nbsp;lenalidomide and dexamethasone alone in results from the phase III ASPIRE trial.

Based on supporting data from the phase III DUO trial and the phase II DYNAMO study, duvelisib has been submitted to the FDA for a full approval&nbsp;for the treatment of patients with relapsed/refractory chronic lymphocytic leukemia/small lymphocytic lymphoma and an accelerated approval for the treatment of patients with relapsed/refractory follicular lymphoma.

Matthew S. Davids, MD, Associate Director, Dana-Farber Cancer Institute Center for Chronic Lymphocytic Leukemia, discusses a multicenter study of ibrutinib (Imbruvica) plus FCR as a frontline therapy for younger patients with chronic lymphocytic leukemia (CLL).&nbsp;<br /> &nbsp;

Lymphoma expert Andrew M. Evens, DO, MSc, FACP, has joined Rutgers Cancer Institute of New Jersey as associate director. He is also serving as medical director of the oncology service line at RWJBarnabas Health. Evens will focus on integrated cancer care delivery in his roles across both institutions.

Patients with relapsed/refractory myeloma&nbsp;who had prior exposure to lenalidomide (Revlimid) experienced a significant improvement in&nbsp;progression-free survival with pomalidomide (Pomalyst) added to the combination of bortezomib (Velcade) and low-dose dexamethasone,&nbsp;according to findings from the phase III OPTIMISMM trial.

Matthew S. Davids, MD, MMSc, recently discussed the treatment choices for patients with chronic lymphocytic leukemia, and the factors he considers when choosing a treatment, based on 2 patient cases.

Progression-free survival was improved by nearly 15% with CHOP-RIT compared with R-CHOP alone in previously untreated patients with follicular lymphoma,&nbsp;according to findings from the phase III SWOG-S0016 trial published in the <em>Journal of Clinical Oncology</em>.

Four US studies of&nbsp;BPX-501 have been halted by the FDA after&nbsp;3 patients developed encephalopathy possibly related to treatment with the&nbsp;novel cellular immunotherapy for cancers and orphan inherited blood disorders.

Anna Sureda, MD, PhD,&nbsp;Head of the Clinical Hematology Service at the Institut Catal&agrave; d&#39;Oncologia &ndash; Hospitalet de Llobregat in Barcelona, discusses the phase III ECHELON-1 study exploring brentuximab vedotin plus doxorubicin, vinblastine, dacarbazine (A+AVD) versus ABVD in patients with previously untreated stage III or IV Hodgkin lymphoma.&nbsp;

Phyllis McKiernan, a nurse practitioner at John Theurer Cancer Center, Hackensack Medical Center, discusses a study of outcomes of autologous stem cell transplantation in very elderly patients with multiple myeloma.

Pfizer has announced that PF-05280586, a biosimilar for rituximab, has delivered positive top-line results, meeting its primary endpoint for overall response rate in the&nbsp;in the phase III REFLECTIONS B3281006 trial for patients with follicular lymphoma.