Evidence map›Paper›PMID 27002115›Full record

ArticleBlood2016

Treatment of multiple myeloma with high-risk cytogenetics: a consensus of the International Myeloma Working Group.

Pieter Sonneveld, Hervé Avet-Loiseau, Sagar Lonial, Saad Usmani, David Siegel, Kenneth C Anderson, Wee-Joo Chng, Philippe Moreau, Michel Attal, Robert A Kyle and 11 more

3 registry-linked trialsOpen access · bronzeAbstract readConsensus Statement
In one paragraph

Article in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 505 papers, 13 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
505citing papers in PubMed, 13 pooled it
57.8field-weighted citation impact, top 1% of its field
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.

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
NCT05849610 phase2active not recruitingnot on this mapstarted 2023, after this paper: background citation

An Open Label, Multicenter, Phase 2, Pilot Study, Evaluating Early Treatment With Bispecific T-cell Redirectors (Teclistamab and Talquetamab) in the Frontline Therapy of Newly Diagnosed High-risk Multiple Myeloma

TypeinterventionalSponsorPETHEMA FoundationRan2023 to 2029Enrolled30ConditionsHigh-Risk de Novo Multiple MyelomaArmsDaratumumab, Bortezomib, Lenalidomide, Teclistamab, Talquetamab
NCT07045168 not yet recruitingnot on this mapstarted 2025, after this paper: background citation

Risk-adapted Therapeutic Strategy in +1q NDMM: a Prospective, Multicenter Study

TypeobservationalSponsorFengYan JinRan2025 to 2029Enrolled200ConditionsMultiple MyelomaArmsrisk-scoring model
3 · Its place in the literature

Who cites it

505 citing papers in PubMed, 13 syntheses or guidelines pooled it, 914 citations in OpenAlex.

  1. Pooled it
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  4. Co-Occurrence of Cytogenetic Abnormalities and High-Risk Disease in Newly Diagnosed and Relapsed/Refractory Multiple Myeloma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
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  13. Prognostic value ofClinical and experimental medicine · 2023
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  14. Trial
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445 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

21 authors at 20 institutions in 8 countries.

Pieter SonneveldDepartment of Hematology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands;
Hervé Avet-LoiseauLaboratory for Genomics in Myeloma, University Cancer Center of Toulouse, Toulouse, France;
Sagar LonialWinship Cancer Institute, Emory University Medical School, Atlanta, GA;
Saad UsmaniLevine Cancer Institute/Carolinas Healthcare System, Charlotte, NC;
David SiegelJohn Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ;
Kenneth C AndersonJerome Lipper Multiple Myeloma Center, Dana-Farber Cancer Institute, Boston, MA;
Wee-Joo ChngDivision of Hematology, National University Cancer Institute, Singapore;
Philippe MoreauDepartment of Hematology, University Hospital, Nantes, France;
Michel AttalDepartment of Hematology, Purpan University Hospital, Toulouse, France;
Robert A KyleDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Minneapolis, MN;
Jo CaersDepartment of Hematology, Centre Hospitalier Universitaire de Liège, Liège, Belgium;
Jens HillengassMedical Clinic V, Section for Multiple Myeloma, University of Heidelberg, Heidelberg, Germany;
Jesús San MiguelClinica Universidad de Navarra, Centro de Investigación Médica Aplicada, Pamplona, Spain;
Niels W C J van de DonkDepartment of Hematology, Free University Medical Center Amsterdam, Amsterdam, The Netherlands;
Hermann EinseleMedical Clinic 2, Universitätsklinik Würzburg, Würzburg, Germany;
Joan BladéUniversity Hospital Clinic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain;
Brian G M DurieInternational Myeloma Foundation, North Hollywood, CA;
Hartmut GoldschmidtUniversity Hospital Heidelberg and National Center for Tumor Diseases Heidelberg, Heidelberg, Germany;
María-Victoria MateosDepartment of Hematology, University Hospital of Salamanca, Salamanca, Spain;
Antonio PalumboMyeloma Unit, University of Torino, Torino, Italy; and.
Robert OrlowskiDivision of Cancer Medicine, Department of Lymphoma/Myeloma, MD Anderson Cancer Center, Houston, TX.
Centre de Recherche en Cancérologie de Toulouse · FRCentre Hospitalier Universitaire de Liège · BECentre Hospitalier Universitaire de Nantes · FRClinica Universidad de Navarra · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESDana-Farber Cancer Institute · USEmory University · USErasmus MC Cancer Institute · NLHackensack University Medical Center · USHeidelberg University · DEHôpital Purpan · FRInternational Myeloma Foundation · USLevine Cancer Institute · USMayo Clinic in Arizona · USNational University Cancer Institute, Singapore · SGThe University of Texas MD Anderson Cancer Center · USUniversidad de Salamanca · ESUniversitätsklinikum Würzburg · DEUniversity Hospital Heidelberg · DEUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The International Myeloma Working Group consensus updates the definition for high-risk (HR) multiple myeloma based on cytogenetics Several cytogenetic abnormalities such as t(4;14), del(17/17p), t(14;16), t(14;20), nonhyperdiploidy, and gain(1q) were identified that confer poor prognosis. The prognosis of patients showing these abnormalities may vary with the choice of therapy. Treatment strategies have shown promise for HR cytogenetic diseases, such as proteasome inhibition in combination with lenalidomide/pomalidomide, double autologous stem cell transplant plus bortezomib, or combination of immunotherapy with lenalidomide or pomalidomide. Careful analysis of cytogenetic subgroups in trials comparing different treatments remains an important goal. Cross-trial comparisons may provide insight into the effect of new drugs in patients with cytogenetic abnormalities. However, to achieve this, consensus on definitions of analytical techniques, proportion of abnormal cells, and treatment regimens is needed. Based on data available today, bortezomib and carfilzomib treatment appear to improve complete response, progression-free survival, and overall survival in t(4;14) and del(17/17p), whereas lenalidomide may be associated with improved progression-free survival in t(4;14) and del(17/17p). Patients with multiple adverse cytogenetic abnormalities do not benefit from these agents. FISH data are implemented in the revised International Staging System for risk stratification.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBortezomibChromosome AberrationsCombined Modality TherapyCytogeneticsHematopoietic Stem Cell TransplantationHumansLenalidomideMultiple MyelomaPrognosisRisk FactorsThalidomideTransplantation, AutologousBortezomibLenalidomidepomalidomideThalidomide

Identifiers

PMID27002115
PMCPMC4920674
OpenAlexW2318069817

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.