Evidence map›Paper›PMID 29150421›Full record

Trial reportBlood2018

Final analysis of survival outcomes in the phase 3 FIRST trial of up-front treatment for multiple myeloma.

Thierry Facon, Meletios A Dimopoulos, Angela Dispenzieri, John V Catalano, Andrew Belch, Michele Cavo, Antonello Pinto, Katja Weisel, Heinz Ludwig, Nizar J Bahlis and 29 more

2 registry-linked trialsAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Blood, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 137 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00689936 phase3completednot on this map

A Phase III, Randomized, Open-label, 3-arm Study to Determine the Efficacy and Safety of Lenalidomide(REVLIMID) Plus Low-dose Dexamethasone When Given Until Progressive Disease or for 18 Four-week Cycles Versus the Combination of Melphalan, Prednisone, and Thalidomide Given for 12 Six-week Cycles in Patients With Previously Untreated Multiple Myeloma Who Are Either 65 Years of Age or Older or Not Candidates for Stem Cell Transplantation.

TypeinterventionalSponsorCelgeneRan2008 to 2016Enrolled1,623ConditionsMultiple MyelomaArmsLenalidomide and low-dose dexamethasone, Lenalidomide plus low-dose dexamethasone given for 18 four-week cycles, Melphalan, Prednisone and Thalidomide
NCT05199311 phase1 / phase2suspendednot on this mapstarted 2022, after this paper: background citation

A Phase I/II Study of Carfilzomib, Iberdomide (CC-220) and Dexamethasone (KID) in Patients With Newly Diagnosed Transplant Eligible Multiple Myeloma

TypeinterventionalSponsorHackensack Meridian HealthRan2022 to 2027Enrolled66ConditionsMultiple MyelomaArmsCarfilzomib, Iberdomide, Oral Dexamethasone
3 · Its place in the literature

Who cites it

137 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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77 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

39 authors.

Thierry FaconService des Maladies du Sang, Hôpital Claude Huriez, Lille, France.
Meletios A DimopoulosDepartment of Clinical Therapeutics, National and Kapodistrian University of Athens School of Medicine, Athens, Greece.
Angela DispenzieriMayo Clinic, Rochester, MN.
John V CatalanoFrankston Hospital and Monash University, Frankston, Australia.
Andrew BelchCross Cancer Institute, Edmonton, Canada.
Michele CavoSeragnoli Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
Antonello PintoDepartment of Hematology and Developmental Therapeutics, Hematology/Oncology and Stem Cells Transplantation Unit, National Cancer Institute, Fondazione "Pascale," Naples, Italy.
Katja WeiselDepartment of Hematology, University of Tuebingen, Tuebingen, Germany.
Heinz LudwigWilhelminenspital, Center for Oncology, Vienna, Austria.
Nizar J BahlisSouthern Alberta Cancer Research Institute, University of Calgary, Calgary, Canada.
Anne BanosCentre Hospitalier de la Côte Basque, Bayonne, France.
Mourad TiabDepartment of Hematology, University Hospital, La Roche Sur Yon, France.
Michel DelforgeUniversity Hospital Leuven, Leuven, Belgium.
Jamie D CavenaghBarts Health National Health Service Trust, London, United Kingdom.
Catarina GeraldesHospitais da Universidade de Coimbra, Coimbra, Portugal.
Je-Jung LeeChonnam National University Hwasun Hospital, Jeollanamdo, South Korea.
Christine ChenPrincess Margaret Hospital, Toronto, Canada.
Albert OriolInstitut Català d'Oncologia and Institut Josep Carreras, Hospital Germans Trias i Pujol, Badalona, Spain.
Javier De La RubiaHospital Dr. Peset, Valencia, Spain.
Darrell WhiteQueen Elizabeth II Health Sciences Centre, Halifax, Canada.
Daniel BinderKantonsspital Winterthur, Winterthur, Switzerland.
Jin LuPeking University People's Hospital, Beijing, China.
Kenneth C AndersonDana-Farber Cancer Institute, Boston, MA.
Philippe MoreauDepartment of Hematology, University of Nantes, Nantes, France.
Michel AttalInstitut Universitaire du Cancer, Toulouse-Oncopole, France.
Aurore PerrotCentre Hospitalier Régional Universitaire de Nancy, Université de Lorraine, Nancy, France.
Bertrand ArnulfHopital Saint Louis, Paris, France.
Lugui QiuBlood Disease Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Tianjin, China.
Murielle RousselCentre Hospitalier Universitaire Purpan/Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
Eileen BoyleService des Maladies du Sang, Hôpital Claude Huriez, Lille, France.
Salomon ManierService des Maladies du Sang, Hôpital Claude Huriez, Lille, France.
Mohamad MohtyHôpital Saint-Antoine, Paris, France.
Herve Avet-LoiseauUnite de Genomique du Myelome, Centre Hospitalier Universitaire Rangueil, Toulouse, France.
Xavier LeleuHôpital de la Milétrie, Centre Hospitalier Universitaire INSERM, Poitiers, France.
Annette Ervin-HaynesCelgene Corporation, Summit, NJ.
Guang ChenCelgene Corporation, Summit, NJ.
Vanessa HouckCelgene Corporation, Summit, NJ.
Lotfi BenboubkerCentre Hospitalier Universitaire Hôpital Bretonneau, Tours Cedex, France; and.
Cyrille HulinBordeaux Hospital University Center (Centre Hospitalier Universitaire), Bordeaux, France.

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Rafael Fonseca · 2015 to 2026
$25.5M
NCI NIH HHS P50 CA186781
6 · The paper itself

Abstract

This FIRST trial final analysis examined survival outcomes in patients with transplant-ineligible newly diagnosed multiple myeloma (NDMM) treated with lenalidomide and low-dose dexamethasone until disease progression (Rd continuous), Rd for 72 weeks (18 cycles; Rd18), or melphalan, prednisone, and thalidomide (MPT; 72 weeks). The primary endpoint was progression-free survival (PFS; primary comparison: Rd continuous vs MPT). Overall survival (OS) was a key secondary endpoint (final analysis prespecified ≥60 months' follow-up). Patients were randomized to Rd continuous (n = 535), Rd18 (n = 541), or MPT (n = 547). At a median follow-up of 67 months, PFS was significantly longer with Rd continuous vs MPT (hazard ratio [HR], 0.69; 95% confidence interval [CI], 0.59-0.79;

Indexed as

Antineoplastic AgentsHumansMultiple MyelomaProgression-Free SurvivalSurvival AnalysisTreatment OutcomeAntineoplastic Agents

Identifiers

PMID29150421
PMCPMC5774211

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.