Evidence map›Paper›PMID 41216847›Full record

ArticleEuropean journal of haematology2026

Prognostic Impact of the Hevylite Assay in Patients With IgG or IgA Multiple Myeloma Treated Within the GMMG-MM5 Trial.

Tim Richardson, Elias Mai, Ekaterina Menis, Axel Benner, Diana Tichy, Kaya Miah, Mathias Hänel, Britta Besemer, Amelie Boquoi, Igor Wolfgang Blau and 13 more

Abstract read
In one paragraph

Article in European journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

23 authors.

Tim RichardsonDepartment of Internal Medicine I, University Hospital Cologne, Cologne, Germany.ORCID https://orcid.org/0009-0006-3588-6376
Elias MaiHeidelberg Myeloma Center, Internal Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital, Heidelberg, Germany.ORCID https://orcid.org/0000-0002-6226-1252
Ekaterina MenisHeidelberg Myeloma Center, Internal Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital, Heidelberg, Germany.ORCID https://orcid.org/0000-0002-5539-580X
Axel BennerDivision of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID https://orcid.org/0000-0002-7238-6956
Diana TichyDivision of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Kaya MiahDivision of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID https://orcid.org/0000-0002-0265-3529
Mathias HänelDepartment of Internal Medicine III, Chemnitz, Germany.ORCID https://orcid.org/0000-0002-4767-3275
Britta BesemerDepartment of Hematology, Oncology and Immunology, University Hospital Tübingen, Tübingen, Germany.
Amelie BoquoiDepartment of Hematology, University Clinic Essen, Essen, Germany.
Igor Wolfgang BlauMedical Clinic, Charité University Medicine Berlin, Berlin, Germany.
Christian S MichelDepartment of Internal Medicine III, University Medical Center Mainz, Mainz, Germany.ORCID https://orcid.org/0009-0004-1596-3763
Hans Walter LindemannDepartment of Hematology and Oncology, Hagen, Germany.ORCID https://orcid.org/0000-0001-9836-7932
Snjezana JanjetovicDepartment of Hematology and Cell Therapy, Helios Klinikum Berlin-Buch, Berlin, Germany.
Peter BrossartDepartment of Internal Medicine, Oncology, Hematology, Cell- and Immunotherapies, Clinical Immunology and Rheumatology, University Hospital Bonn, Bonn, Germany.ORCID https://orcid.org/0000-0001-5133-1094
Helga BernhardInternal MedicineV, Darmstadt, Germany.
Peter ReimerKliniken Essen-Mitte, Klinik für Hämatologie, Internistische Onkologie Und Stammzelltransplantation Pattbergstr, Essen, Germany.
Hans SalwenderAsklepios Tumorzentrum Hamburg, Hamburg, Germany.ORCID https://orcid.org/0000-0001-7803-0814
Dirk HoseLaboratory of Hematology and Immunology & Labor für Myelomforschung, Vrije Universiteit Brussel, Jette, Belgium.
Anja SeckingerLaboratory of Hematology and Immunology & Labor für Myelomforschung, Vrije Universiteit Brussel, Jette, Belgium.
Marc RaabHeidelberg Myeloma Center, Internal Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital, Heidelberg, Germany.
Hartmut GoldschmidtInternal Medicine V, Hematology, Oncology and Rheumatology, GMMG Study Group at the Heidelberg University Hospital, Heidelberg, Germany.ORCID https://orcid.org/0000-0003-0961-0035
Christof ScheidDepartment of Internal Medicine I, University Hospital Cologne, Cologne, Germany.ORCID https://orcid.org/0009-0007-6539-226X
German‐Speaking Myeloma Multicenter Group (GMMG) HD5 Investigators

Funding

Binding Site GmbH is part of Thermo Fisher ScientificCelgeneChugai PharmaceuticalJohnson and Johnson
6 · The paper itself

Abstract

Response assessment during treatment of multiple myeloma (MM) typically relies on immunofixation and serum electrophoresis. However, low levels of IgG and especially IgA paraprotein are difficult to quantify reliably. The Hevylite Assay quantifies the kappa and lambda fractions of IgG and IgA separately and is useful to determine response to therapy. Using serum samples of 360 evaluable patients from the prospective GMMG-MM5 trial (EudraCT-No. 2010-019173-16) we assessed the normalization of the kappa/lambda ratio with the Hevylite Assay (HLCr) at baseline, after induction, mobilization, autologous blood stem cell transplantation, consolidation and every three months during maintenance or follow-up within two years after the end of consolidation. We observed a steady increase in the proportion of patients with normalized HLCr over the course of therapyAchieving HLCr normalization any time until the end of consolidation was associated with a trend towards a prolonged progression-free survival (PFS; hazard ratio (HR) = 0.75, 95% confidence interval (95% CI) = 0.56-1.01, p = 0.06) but not overall survival (OS; HR = 0.94, 95% CI = 0.69-1.26, p = 0.66) in multivariable time-dependent Cox regression analyses. Using a landmark analysis from the end of consolidation there was again a marginally statistically significant effect of HLCr normalization by the end of consolidation on PFS using a multivariable Cox model on the subset of the two study arms with continuous lenalidomide maintenance (HR 0.61, 95% CI 0.37-1.02, p = 0.06). No such effect was observed in study arms in which maintenance was only applied to patients not in CR at the end of consolidation. In conclusion, our analysis of the Hevylite Assay in patients with IgG or IgA myeloma from the GMMG-MM5 study did not find evidence to support the general use of HLCr normalization as a response parameter for predicting PFS or OS. However, the differential effects of HLCr normalization depending on the way in which treatment was adapted to response may be of interest for future study designs on response-adapted therapy. Trial Registration: ISRCTN05622749.

Indexed as

Immunoglobulin AImmunoglobulin GMultiple MyelomaAdultAgedAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansImmunoglobulin kappa-ChainsImmunoglobulin lambda-ChainsMaleMiddle AgedPrognosisTreatment OutcomeImmunoglobulin AImmunoglobulin GImmunoglobulin kappa-ChainsImmunoglobulin lambda-Chainsheavylite assaymultiple myelomaprognostic biomarker

Identifiers

PMID41216847
PMCPMC12861712

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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.