A plain language summary of the final analysis of the GRIFFIN study of daratumumab plus lenalidomide, bortezomib, and dexamethasone for people with newly diagnosed multiple myeloma.

D-RVd GRIFFIN daratumumab lay summary multiple myeloma newly diagnosed plain language summary transplant eligible

Journal

Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629

Informations de publication

Date de publication:
25 Oct 2024
Historique:
medline: 25 10 2024
pubmed: 25 10 2024
entrez: 25 10 2024
Statut: aheadofprint

Résumé

This summary describes the final analysis of the GRIFFIN study. In this study, participants were newly diagnosed with a type of blood and bone marrow cancer called multiple myeloma, had never received any treatment, and were able to undergo an autologous stem cell transplant. The GRIFFIN study looked at adding the drug daratumumab (D) to a combination of standard treatments called RVd (lenalidomide [R], bortezomib [V], and dexamethasone [d]) during the treatment phases induction and consolidation, followed by daratumumab and lenalidomide (D-R) maintenance. Participants also received an autologous stem cell transplant to further help reduce multiple myeloma. The GRIFFIN study looked at whether D-RVd followed by D-R maintenance was better at killing multiple myeloma cells compared with RVd on its own followed by R maintenance on its own, and if treatments were safe. This summary also describes results from 2 other GRIFFIN publications: one that looked at participants with certain multiple myeloma characteristics or demographic factors that are associated with worse outcomes, and another that looked at how treatments impacted the participants' quality of life. At the time of the final analysis of GRIFFIN, participants who were treated with D-RVd followed by D-R maintenance had very low (undetectable) levels of multiple myeloma cells and multiple myeloma markers (biological signs) and were more likely to be alive without the multiple myeloma getting worse or coming back compared with participants who received standard RVd treatment followed by R maintenance. There was also a pattern of similar benefits achieved by participants who were at risk for worse outcomes. Additionally, participants who received D-RVd treatment followed by D-R maintenance reported less pain, less fatigue (extreme tiredness), and greater improvements in their ability to conduct daily physical activities. While some side effects (unwanted or unexpected effects of treatment) were higher with D-RVd, side effects in both groups were as expected, and adding daratumumab did not reduce a participant's ability to handle treatment. Results of the GRIFFIN study showed that D-RVd treatment followed by D-R maintenance was better at treating multiple myeloma than the standard treatment of RVd followed by R maintenance in adults with a new diagnosis of multiple myeloma who were able to receive an autologous stem cell transplant, with no unexpected side effects of treatment.

Identifiants

pubmed: 39452950
doi: 10.1080/14796694.2024.2408909
doi:

Banques de données

ClinicalTrials.gov
['NCT02874742']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-25

Auteurs

Peter M Voorhees (PM)

Levine Cancer Institute, Atrium Health Wake Forest University School of Medicine, Charlotte, NC, USA.

Douglas W Sborov (DW)

Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.

Jacob Laubach (J)

Dana-Farber/Partners CancerCare, Harvard Medical School, Boston, MA, USA.

Jonathan L Kaufman (JL)

Winship Cancer Institute, Emory University, Atlanta, GA, USA.

Brandi Reeves (B)

Department of Medicine, University of North Carolina Chapel Hill, Chapel Hill, NC, USA.

Cesar Rodriguez (C)

Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Rebecca Silbermann (R)

Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.

Luciano J Costa (LJ)

University of Alabama at Birmingham Hospital, Birmingham, AL, USA.

Larry D Anderson (LD)

Myeloma, Waldenstrom's & Amyloidosis Program, Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.

Nitya Nathwani (N)

Judy & Bernard Briskin Center for Multiple Myeloma Research, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.

Nina Shah (N)

Department of Medicine, University of California San Francisco, San Francisco, CA, USA.

Naresh Bumma (N)

Division of Hematology, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.

Yvonne A Efebera (YA)

OhioHealth, Blood & Marrow Transplant, Columbus, OH, USA.

Sarah A Holstein (SA)

Division of Oncology & Hematology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA.

Caitlin Costello (C)

Moores Cancer Center, University of California San Diego, La Jolla, CA, USA.

Andrzej Jakubowiak (A)

University of Chicago Medical Center, Chicago, IL, USA.

Tanya M Wildes (TM)

Division of Oncology & Hematology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA.

Robert Z Orlowski (RZ)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Kenneth H Shain (KH)

Department of Malignant Hematology, H. Lee Moffitt Cancer Center, Tampa, FL, USA.

Andrew J Cowan (AJ)

Division of Medical Oncology, University of Washington, Seattle, WA, USA.

Shira Dinner (S)

Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL, USA.

Katharine S Gries (KS)

Janssen Research & Development, LLC, Raritan, NJ, USA.

Huiling Pei (H)

Janssen Research & Development, LLC, Titusville, NJ, USA.

Annelore Cortoos (A)

Janssen Scientific Affairs, LLC, a Johnson & Johnson company, Horsham, PA, USA.

Sharmila Patel (S)

Janssen Scientific Affairs, LLC, a Johnson & Johnson company, Horsham, PA, USA.

Thomas S Lin (TS)

Janssen Scientific Affairs, LLC, a Johnson & Johnson company, Horsham, PA, USA.

Saad Z Usmani (SZ)

Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Paul G Richardson (PG)

Dana-Farber/Partners CancerCare, Harvard Medical School, Boston, MA, USA.

Classifications MeSH