Our own Zach Roberts provides his perspective on how allogeneic CAR T products may be a solution to problems facing autologous CAR T products for patients with #CLL in the latest issue of Cell & Gene. #Immunotherapy#CART
The Path Forward for CLL is Allogeneic
https://lnkd.in/euvZhyWK
By Zachary J Roberts MD PhD, Executive Vice President, Research & Development, and Chief Medical Officer, Allogene Therapeutics
Chronic lymphocytic leukemia (CLL) remains a disease that is managed, not one that is often cured.
Zachary's insights on allogeneic CAR T products addressing challenges in CLL are crucial for advancing treatment options. Allogeneic approaches offer promising solutions where autologous methods face limitations. #Immunotherapy #CART
Could your patients be eligible for the KOMET-008 clinical trial aimed at evaluating ziftomenib, a menin inhibitor, with other existing standard-of-care treatments in relapsed or refractory acute myeloid leukemia? Hematologist-oncologist Harry Erba, MD, PhD, explains the different combinations KOMET-008 will evaluate and how it differs from KOMET-007.
KOMET-008 is OPENING SOON. Learn more: https://lnkd.in/g37mAZZq
Over the last decades, outcomes in B-cell acute lymphoblastic leukemia (B-ALL) have improved enormously thanks to developments in treatment. However, drug resistance and relapse, particularly among adults patients, is still a big challenge.
This issue of Haematologica reports on a new potential therapeutic target for B-ALL: the mucosa-associated lymphoid tissue lymphoma translocation protein 1 (MALT1).
https://lnkd.in/d8t4pABj
Venetoclax Combined with Intensive Chemotherapy: A New Hope for Refractory and/or Relapsed Acute Myeloid Leukemia? Authors: Ramy Rahmé & Thorsten Braun
I am happy to share with you our latest opinion article/review on the treatment of refractory/relapsed acute myeloid leukemia with intensive chemotherapy approaches. In particular, we focus on chemotherapeutic regimens incorporating the BCL2 inhibitor venetoclax. Available data are indeed scarce on this matter. Still, they show higher rates of complete remission than historical reports, bridging a substantial number of patients to allogeneic transplant with the potential of cure.
Website:
More than 30 years ago, Bispecific T-cell Engager (BiTE®) technology was developed with the goal of finding new ways to help people facing the toughest-to-treat cancers.
These efforts came to fruition nearly a decade ago, when Amgen's novel immunotherapy became the first globally approved BiTE® molecule, expanding options for people with advanced B-cell lineage acute lymphoblastic leukemia (B-ALL), a patient population with historically dismal outcomes and limited treatment options.
Over the past ten years, it’s been inspiring to see our T-cell engager impact relapsed or refractory and measurable residual disease (MRD)-positive B-ALL patients.
Now with @FDA approval for Ph-negative B-ALL patients regardless of their MRD status, Amgen is again poised to transform possibilities for people with this aggressive blood cancer. Read more👇#MyCompany
Today, the U.S. FDA granted approval for Amgen’s Bispecific T-cell Engager (BiTE®) immunotherapy in patients with CD19-positive Ph-negative B-cell precursor acute lymphoblastic leukemia (B-ALL) in the consolidation phase.
🔗 Press release: https://amgen.ly/3VHKOKX
Their abstract: Despite significant advances over recent years, the treatment of T cell acute lymphoblastic leukemia (T-ALL) remains challenging. We have recently shown that a subset of T-ALL cases exhibited constitutive activation of the lymphocyte-specific protein tyrosine kinase (LCK) and were consequently responsive to treatments with LCK inhibitors and degraders such as dasatinib and dasatinib-based PROTACs. Here we report the design, synthesis and in vitro/vivo evaluation of SJ45566, a potent and orally bioavailable LCK PROTAC.
Despite significant advances over recent years, the treatment of T cell acute lymphoblastic leukemia (T-ALL) remains challenging. We have recently shown that a subset of T-ALL cases exhibited constitutive activation of the lymphocyte-specific protein tyrosine kinase (LCK) and were consequently responsive to treatments with LCK inhibitors and degraders such as dasatinib and dasatinib-based #PROTACs. Here we report the design, synthesis and in vitro/vivo evaluation of #SJ45566, a potent and orally bioavailable LCK #PROTAC.
#Protac#PDC#SmallMolecule#Medchem#Medcinal#FFS#FTE#CDMO#CMC
New from Immune-Onc Therapeutics at #EHA2024! Today, we will present additional positive interim Phase 1b expansion cohort data for IO-202 in patients with chronic myelomonocytic leukemia (#CMML). The study shows early and sustained complete remissions among CMML patients, regardless of their prognosis or mutation status. Learn more:
https://lnkd.in/gZgdrvr6
Professor and Founding Chair, Dept. of Molecular Diagnostics and Experimental Therapeutics; Associate Director of Basic Sciences, City of Hope Comprehensive Cancer Center; Director, Biotech Innovations
Curcumin helps overcome resistance to Lenvatinib in hepatocellular cancer.
The incidence of #hepatocellular carcinoma (HCC) is rising worldwide, and the therapeutic options are limited in this malignancy.
#Lenvatinib is a multi‐kinase inhibitor that is often used to treat patients with HCC. However, the majority of patients develop
resistance to Lenvatinib. In a recent study published in the journal Cells, our team reported that treatment with #Curcumin could
help overcome Lenvatinib resistance in HCC, highlighting the potential use of this potent nutraceutical as an adjunctive treatment in
this malignancy.
Innovative Leadership in Talent Solutions: Founder & CEO of Recruits Lab & BioJobs Lab, Driving Organizational Success through Cutting-Edge Recruitment Strategies.
4wZachary's insights on allogeneic CAR T products addressing challenges in CLL are crucial for advancing treatment options. Allogeneic approaches offer promising solutions where autologous methods face limitations. #Immunotherapy #CART