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: Daratumumab-based regimens represent the gold-standard therapy for newly diagnosed AL amyloidosis patients. However, there are few studies about the efficacy of this treatment in real life. : This study included 99 patients: 27 (27.3%) received daratumumab and proteasome inhibitor-based schemes, 46 (46.4%) were treated with proteasome inhibitors and/or immunomodulator-based regimens, and 26 (26.3%) were treated with chemotherapy. : Patients receiving daratumumab and proteasome inhibitor-based regimens achieved higher rates of partial haematological responses or better (100.0% vs. 78.3% vs. 58.3%; = 0.009 and < 0.001) and complete responses (74.1% vs. 37.0% vs. 12.5%; = 0.003 and < 0.001) than the proteasome inhibitors and/or immunomodulators and chemotherapy groups, respectively. Daratumumab and proteasome inhibitor-based schemes resulted in a shorter time to haematological response (1 month to partial response or better and 4 months to complete response). Moreover, in the group treated with daratumumab and proteasome inhibitor-based regimens, there was a trend of obtaining better and faster organ responses. The benefit of daratumumab and proteasome inhibitor-based regimens was that they resulted in an improvement in progression-free survival (not reached) compared to the proteasome inhibitor and chemotherapy groups (18 months; = 0.022 and 6 months; = 0.002). In addition, the clinical benefit was consistent in patients with Mayo Clinic stages III-IV. : This study supports the efficacy and superiority of adding daratumumab to the frontline treatment over proteasome inhibitor-based regimens and chemotherapy in AL amyloidosis, including in advanced cardiac disease.
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http://dx.doi.org/10.3390/cancers17091440 | DOI Listing |
Cells
August 2025
Division of Hematology and Oncology, Department of Medicine, Loyola University Medical Center, Maywood, IL 60153, USA.
Despite the increasing number of novel therapies to treat newly diagnosed multiple myeloma (NDMM), preventing skeletal-related events (SREs) remains a challenge. This review summarizes the mechanistic causes of myeloma bone disease, data supporting the use of bisphosphonates and RANKL inhibitors, and the optimal management of preventing SREs in NDMM patients. Both zoledronic acid (ZA) and denosumab are acceptable treatment options with comparable safety and efficacy profiles.
View Article and Find Full Text PDFCancers (Basel)
April 2025
Hematology Department, University Hospital of Salamanca, Cancer Research Center-IBMCC (USAL-CSIC), Instituto de Investigación Biomédica de Salamanca (IBSAL), CIBERONC, 37007 Salamanca, Spain.
: Daratumumab-based regimens represent the gold-standard therapy for newly diagnosed AL amyloidosis patients. However, there are few studies about the efficacy of this treatment in real life. : This study included 99 patients: 27 (27.
View Article and Find Full Text PDFJ Hematol Oncol
May 2025
School of Medicine, Taizhou University, Taizhou, Zhejiang, 318000, People's Republic of China.
Selective elimination of proteins associated with the pathogenesis of diseases is an emerging therapeutic modality with distinct advantages over traditional inhibitor-based approaches. This strategy, called targeted protein degradation (TPD), is based on hijacking the cellular proteolytic machinery using chimeric degrader molecules that physically link the target protein of interest with the degradation effectors. The TPD era began with the development of PROteolysis TAtrgeting Chimeras (PROTACs) in 2001, with various methods and applications currently available.
View Article and Find Full Text PDFHaematologica
September 2025
Department of Supportive Care Medicine, Hematology/HCT, City of Hope, CA.
Plasma cell leukemia (PCL) is a rare and aggressive plasma cell disorder with a short survival duration despite the use of novel therapeutics. PCL remains an understudied disease for which there is no current standard of care treatment. Knowledge on optimal novel drug sequencing, including the role and timing of hematopoietic stem cell transplant as primary and salvage therapy is needed.
View Article and Find Full Text PDFPlasmacytoma can manifest as a solitary pulmonary mass, which can be accurately diagnosed through a combination of Bone scan, serum protein electrophoresis, computed tomography (CT)-guided biopsy and bone marrow biopsy. Notably, this case diagnosed with multiple myeloma (MM) with extramedullary plasmacytoma (EMP) demonstrated an exceptional treatment response to radiotherapy and proteasome inhibitor-based chemotherapy.
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