Year-End Sale is Live! Find Exclusive Prices on the Best Selling Pharma & MedTech Reports.Check Now!

Page Banner for mobile screens

Decoding the Future of Hematologic Cancer: A First Look at Game-Changing Research from EHA 2024's High Priority Sessions

Hematologic Cancer Preview Content | EHA 2024

The EHA congress typically features a diverse range of hematologic disorders, including leukemia, lymphoma, myeloma, bleeding disorders, and hematopoietic stem cell transplantation, offering a comprehensive overview of the current state of both research and clinical practice in hematology. Furthermore, it offers insights into future directions and obstacles in the field.

Top pharmaceutical companies are gearing up for the conference, ready to present initial, updated, and final results. Key players like GlaxoSmithKline, AstraZeneca, Roche, Electra Therapeutics, Novartis, Agios Pharmaceuticals, Sanofi, and others will present High Priority Late Breaking and Plenary Session Abstracts.

These sessions are on the verge of potentially transforming patient care in the future. They carry the potential for substantial progress, aiming to positively impact the treatment landscape of hematologic cancer.

BLENREP (belantamab mafodotin) was initially granted conditional marketing authorization in the US and EU based on results from the DREAMM-2 trial, a Phase II, open-label, randomized, two-arm study, with the primary efficacy measure being the overall response rate (ORR). However, the subsequent Phase III DREAMM-3 trial did not achieve its primary endpoint of progression-free survival (PFS), leading the European Medicines Agency (EMA) and US Food and Drug Administration (FDA) to revoke the conditional marketing authorization. GSK recently published detailed positive results from DREAMM-7 and announced that the DREAMM-8 trial also met its primary endpoint of PFS. So it would be interesting to see the full results from the DREAMM-8 trial as these positive results could mark BLENREP’s potential return as a promising treatment for relapsed refractory multiple myeloma.

Sanofi will also present the data of SARCLISA (isatuximab) from the IMROZ trial, during the plenary scientific session on June 15, selected as one of the top six abstracts to be featured at the congress. Results from IMROZ will form the basis of a future regulatory submission for patients with newly diagnosed multiple myeloma not eligible for transplant.

Key Abstracts

List of Key Late Breaking Abstracts (LBA) and Plenary sessions

Therapy

Name

Company

Class

Abstract ID

Abstract Type

Session Date/

Time

Abstract Title

Author

BLENREP (belantamab mafodotin)

BCMA- ADC

LB3440

Oral

June 16, 2024 (10:00 - 10:15 CEST)

RESULTS FROM THE RANDOMIZED PHASE 3 DREAMM-8 STUDY OF BELANTAMAB MAFODOTIN PLUS POMALIDOMIDE AND DEXAMETHASONE VS POMALIDOMIDE PLUS BORTEZOMIB AND DEXAMETHASONE IN REPALPSED/REFRACTORY MULTIPLE MYELOMA

Meletios Dimopoulos

CALQUENCE (acalabrutinib)

AstraZeneca logo

BTK inhibitor.

LB3439

Oral

June 16, 2024 (9:45 - 10:00 CEST)

ACALABRUTINIB PLUS BENDAMUSTINE AND RITUXIMAB IN UNTREATED MANTLE CELL LYMPHOMA: RESULTS FROM THE PHASE 3, DOUBLE-BLIND, PLACEBO-CONTROLLED ECHO TRIAL

Michael Wang

COLUMVI (glofitamab)

CD20 x CD3  bispecific antibody

LB3438

Oral 

June 15, 2024 (16:00 - 16:45 CEST)

PHASE 3 STUDY RESULTS OF ISATUXIMAB, BORTEZOMIB, LENALIDOMIDE, AND DEXAMETHASONE (ISA-VRD) VERSUS VRD FOR TRANSPLANT-INELIGIBLE PATIENTS WITH NEWLY DIAGNOSED MULTIPLE MYELOMA (IMROZ)

Thierry Facon

ELA026

IgG1 SIRP-directed mAb

LB3442

Oral

June 16, 2024 (10:30 - 10:45 CEST)

ELA026 TARGETING OF SIRP(+) IMMUNE CELLS RESULTS IN A HIGHRESPONSE RATE AND IMPROVED 2-MONTH SURVIVAL OF TREATMENT-NAIVEMALIGNANCY-ASSOCIATED HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN A PHASE 1 STUDY

Abhishek Maiti

Asciminib

Tyrosine kinase inhibitor

S103

Oral

June 15, 2024 (15:30 - 15:45 CEST)

ASCIMINIB (ASC) PROVIDES SUPERIOR EFFICACY AND EXCELLENT SAFETY AND TOLERABILITY VS TYROSINE KINASE INHIBITORS (TKI) IN NEWLY DIAGNOSED CHRONIC MYELOID LEUKEMIA (CML) IN THE PIVOTAL ASC4FIRST STUDY

Andreas Hochhaus

Mitapivat

Pyruvate kinase activator

S104

Oral

June 15, 2024 (15:45 - 16:00 CEST)

ENERGIZE: A GLOBAL PHASE 3 STUDY OF MITAPIVAT DEMONSTRATING EFFICACY AND SAFETY IN ADULTS WITH ALPHA- OR BETA-NON–TRANSFUSION-DEPENDENT THALASSEMIA

Ali T. Taher

Arsenic Trioxide (ATO) Combined to ATRA and Idarubicin

Antineoplastics

S102

Oral

June 15, 2024 (15:15 - 15:30 CEST)

FIRST RESULTS OF THE APOLLO TRIAL: A RANDOMIZED PHASE III STUDY TO COMPARE ATO COMBINED WITH ATRA VERSUS STANDARD AIDA REGIMEN FOR PATIENTS WITH NEWLY DIAGNOSED, HIGH-RISK ACUTE PROMYELOCYTIC LEUKEMIA

Uwe Platzbecker

Isatuximab

Anti-CD38 mAb

S100

Oral

June 15, 2024 (14:45 - 15:00 CEST)

PHASE 3 STUDY RESULTS OF ISATUXIMAB, BORTEZOMIB, LENALIDOMIDE, AND DEXAMETHASONE (ISA-VRD) VERSUS VRD FOR TRANSPLANT-INELIGIBLE PATIENTS WITH NEWLY DIAGNOSED MULTIPLE MYELOMA (IMROZ)

Thierry Facon

 

Tags:

Executive Summary

The EHA congress typically features a diverse range of hematologic disorders, including leukemia, lymphoma, myeloma, bleeding disorders, and hematopoietic stem cell transplantation, offering a comprehensive overview of the current state of both research and clinical practice in hematology.

Recent Articles