News and Treatment Updates
Here's where you'll find a regularly updated, broad range of articles written by the AAMDSIF team, allied health organizations and news organizations. By staying well-informed, patients and families are practicing a form of self-support that will help them be more effective self-advocates when engaging with health care providers.
Researchers describe impact of SF3B1 mutations in myelodysplastic syndrome
Originally Published: 09/14/2020
Article Source: External Web Content
SF3B1 mutations occurred more frequently in de novo myelodysplastic syndromes than therapy-related myelodysplastic syndrome, according to results of a phase 2 study presented at Society of Hematologic Oncology Annual Meeting.
Additionally, SF3B1 mutations appeared associated with improved survival among patients with de novo vs. therapy-related myelodysplastic syndrome (MDS). However, among patients with treatment-related disease, those with SF3B1 mutations had better outcomes than those with wild-type SF3B1.
(Article and Charts continue at link)
Talati Highlights “Game-Changing” Potential of Venetoclax/HMA Combos for Elderly AML
Originally Published: 09/08/2020
Article Source: External Web Content
Chetasi Talati, MD, discusses early results from a multicenter chart review examining treatment patterns and outcomes of patients with newly diagnosed AML who received venetoclax/HMA combinations in the real-world setting and the next phase of the ongoing research initiative.
Chetasi Talati, MD
Chetasi Talati, MD
Early data suggest that the low-intensity combination of venetoclax (Venclexta) and hypomethylating agents (HMAs) may be a “game-changer” for patients with relapsed/refractory acute myeloid leukemia (AML), according to Chetasi Talati, MD, especially for older patients who may not...
FDA approves Onureg (azacitidine tablets) for acute myeloid leukemia
Originally Published: 09/01/2020
Article Source: External Web Content
On September 1, 2020, the Food and Drug Administration approved azacitidine tablets (ONUREG®, Celgene Corporation) for continued treatment of patients with acute myeloid leukemia who achieved first complete remission (CR) or complete remission with incomplete blood count recovery (CRi) following intensive induction chemotherapy and are not able to complete intensive curative therapy.
Efficacy was investigated in QUAZAR (NCT01757535), a multicenter, randomized, double-blind, placebo-controlled trial. Patients (n=472) who achieved CR or CRi with intensive induction chemotherapy with or without...
Patient and physician perceptions about blood transfusions in the myelodysplastic syndromes
Originally Published: 09/01/2020
Article Source: External Web Content
Abstract
Background
Little is known about the shared decision-making between patients with transfusion-dependent (TD) myelodysplastic syndromes (MDS) and their physicians about the benefits, risks, and alternatives to reduce the need for blood transfusions.
Methods and Materials
We conducted interviews and two cross-sectional surveys of MDS patients and MDS physicians in the US about the use of blood transfusions and disease-modifying therapies (DMTs). Responses from 157 MDS patients and 109 MDS physicians were analyzed.
Results (continued at link)
Understanding the Impact of Telomere Length and Mutations on Transplant Outcomes
Originally Published: 08/31/2020
Article Source: External Web Content
Advances in Hematologic Malignancies
Issue 12, Summer 2020
— R. Coleman Lindsley, MD, PhD
Identifying patients at high risk of fatal treatment toxicity is a central challenge in allogeneic hematopoietic stem cell transplantation (HSCT). More accurate prediction of non-relapse mortality (NRM) risk could inform clinical decisions about timing and approach to HSCT. Short telomere length impairs the cellular response to genotoxic and replicative stress, and limits the regenerative potential of many tissues, including the gastrointestinal mucosa and bone marrow. We recently completed a study that...
Guideline-based indicators for adult patients with myelodysplastic syndromes
Originally Published: 08/25/2020
Article Source: External Web Content
Key Points
GBIs are measurable elements for quality of care and are currently lacking for adult MDS patients.
We developed a GBI consensus for the domains of diagnosis (n = 14), therapy (n = 8), and provider/infrastructural characteristics (n = 7).
Myelodysplastic syndromes (MDSs) represent a heterogeneous group of hematological stem cell disorders with an increasing burden on health care systems. Evidence-based MDS guidelines and recommendations (G/Rs) are published but do not necessarily translate into better quality of care if adherence is not maintained in daily clinical practice....
TP53 Mutation Status Possesses Prognostic Implications in MDS
Originally Published: 08/14/2020
Article Source: External Web Content
Patients with myelodysplastic syndromes (MDS) who have biallelic TP53 have worse outcomes, such as treatment-resistant disease, rapid disease progression, and low overall survival, versus those with monoallelic mutations, according to results from a study published in Nature Medicine.1
“In recent years, we have characterized which mutations are present in MDS and have established diagnostic tests that map which mutations are present in every patient. This information is used to guide treatment decisions; this is the vision of precision medicine,” Elli Papaemmanuil, PhD, the senior author of...
Clinical characteristics and risk factors associated with COVID-19 severity in patients with haematological malignancies in Italy: a retrospective, multicentre, cohort study
Originally Published: 08/13/2020
Article Source: External Web Content
Background
Several small studies on patients with COVID-19 and haematological malignancies are available showing a high mortality in this population. The Italian Hematology Alliance on COVID-19 aimed to collect data from adult patients with haematological malignancies who required hospitalisation for COVID-19.
Methods
This multicentre, retrospective, cohort study included adult patients (aged ≥18 years) with diagnosis of a WHO-defined haematological malignancy admitted to 66 Italian hospitals between Feb 25 and May 18, 2020, with laboratory-confirmed and symptomatic COVID-19. Data cutoff for...
ASH Issues Guidelines on Newly Diagnosed AML in Older Adults
Originally Published: 08/12/2020
Article Source: External Web Content
In evidence-based guidelines issued by the American Society of Hematology and published in the Aug. 11 issue of Blood Advances, recommendations are presented for the management of newly diagnosed acute myeloid leukemia (AML) in older adults.
Mikkael A. Sekeres, M.D., from the Taussig Cancer Center at the Cleveland Clinic, and colleagues developed evidence-based guidelines to support patients, clinicians, and other health care professionals in their decisions about AML management in older adults.
The recommendations relate to newly diagnosed de novo, treatment-related, and secondary AML in...
American Society of Hematology 2020 guidelines for treating newly diagnosed acute myeloid leukemia in older adults
Originally Published: 08/06/2020
Article Source: External Web Content
Abstract
Background:
Older adults with acute myeloid leukemia (AML) represent a vulnerable population in whom disease-based and clinical risk factors, patient goals, prognosis, and practitioner- and patient-perceived treatment risks and benefits influence treatment recommendations.
Objective:
These evidence-based guidelines of the American Society of Hematology (ASH) are intended to support patients, clinicians, and other health care professionals in their decisions about management of AML in older adults.
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