Literature DB >> 24273135

Mature results of MM-011: a phase I/II trial of liposomal doxorubicin, vincristine, dexamethasone, and lenalidomide combination therapy followed by lenalidomide maintenance for relapsed/refractory multiple myeloma.

Aleksandr Lazaryan1, Mohamad A Hussein, Frederic J Reu, Beth Faiman, Becky Habecker, Mary Ann Karam, Janice Reed, Kimberly Hamilton, Joel Waksman, Kellie Bruening, Gordan Srkalovic, Steven Andresen, Matthew Kalaycio, John W Sweetenham, Ronald Sobecks, Robert Dean, Robert Knight, Jerome B Zeldis, Rachid Baz.   

Abstract

A previous interim report of MM-011, the first study that combined lenalidomide with anthracycline-based chemotherapy followed by lenalidomide maintenance for relapsed and/or refractory multiple myeloma (RRMM), showed promising safety and activity. We report the long-term outcomes of all 76 treated patients with follow-up ≥ 5 years. This single-center phase I/II study administered lenalidomide (10 mg on days 1-21 of every 28-day cycle), intravenous liposomal doxorubicin (40 mg/m(2) on day 1), dexamethasone (40 mg on days 1-4), and intravenous vincristine (2 mg on day 1). After 4-6 planned induction cycles, lenalidomide maintenance therapy was given at the last tolerated dose until progression, with or without 50 mg prednisone every other day. The median number of previous therapies was 3 (range, 1-7); 49 (64.5%) patients had refractory disease. Forty-three (56.6%) patients received maintenance therapy. Grade 3/4 adverse events occurred during induction and maintenance therapy in 48.7% and 25.6% of patients, respectively. Four (5.3%) treatment-related deaths occurred during induction. Responses were seen in 53.0% (at least partial response) and 71.2% (at least minor response) of patients. Overall, median progression-free survival and overall survival were 10.5 and 19.0 months, respectively; in patients with refractory disease these values were 7.5 and 11.3 months, respectively. Lenalidomide with anthracycline-based chemotherapy followed by maintenance lenalidomide provided durable control in patients with RRMM (ClinicalTrials.gov number, NCT00091624).
Copyright © 2013 Wiley Periodicals, Inc.

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Year:  2014        PMID: 24273135     DOI: 10.1002/ajh.23639

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  5 in total

1.  p38 MAPK differentially controls NK activating ligands at transcriptional and post-transcriptional level on multiple myeloma cells.

Authors:  Alessandra Soriani; Cristiana Borrelli; Biancamaria Ricci; Rosa Molfetta; Alessandra Zingoni; Cinzia Fionda; Silvia Carnevale; Maria Pia Abruzzese; Maria Teresa Petrucci; Maria Rosaria Ricciardi; Giuseppe La Regina; Erica Di Cesare; Patrizia Lavia; Romano Silvestri; Rossella Paolini; Marco Cippitelli; Angela Santoni
Journal:  Oncoimmunology       Date:  2016-12-02       Impact factor: 8.110

2.  Venous thromboembolism risk with contemporary lenalidomide-based regimens despite thromboprophylaxis in multiple myeloma: A systematic review and meta-analysis.

Authors:  Rajshekhar Chakraborty; Irbaz Bin Riaz; Saad Ullah Malik; Naimisha Marneni; Alex Mejia Garcia; Faiz Anwer; Alok A Khorana; S Vincent Rajkumar; Shaji Kumar; M Hassan Murad; Zhen Wang; Safi U Khan; Navneet S Majhail
Journal:  Cancer       Date:  2020-01-08       Impact factor: 6.860

Review 3.  Evolving paradigms in the treatment of relapsed/refractory multiple myeloma: increased options and increased complexity.

Authors:  R F Cornell; A A Kassim
Journal:  Bone Marrow Transplant       Date:  2016-01-04       Impact factor: 5.483

Review 4.  Programmed cell death, redox imbalance, and cancer therapeutics.

Authors:  Xiaofeng Dai; Danjun Wang; Jianying Zhang
Journal:  Apoptosis       Date:  2021-07-08       Impact factor: 4.677

Review 5.  Evolving Paradigms in the Management of Multiple Myeloma: Novel Agents and Targeted Therapies.

Authors:  Jeremy T Larsen; Shaji Kumar
Journal:  Rare Cancers Ther       Date:  2015-08-28
  5 in total

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