Evidence map›Paper›PMID 30192814›Full record

ArticlePloS one2018

Prognostic utility of serum free light chain ratios and heavy-light chain ratios in multiple myeloma in three PETHEMA/GEM phase III clinical trials.

Lucia Lopez-Anglada, Cecilia Cueto-Felgueroso, Laura Rosiñol, Albert Oriol, Ana Isabel Teruel, Ana Lopez de la Guia, Enrique Bengoechea, Luis Palomera, Felipe de Arriba, Jose Mariano Hernandez and 17 more

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 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.

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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

27 authors.

Lucia Lopez-AngladaHematology Department, Hospital Universitario 12 de Octubre, CIBERONC, Madrid, Spain.ORCID 0000-0003-1727-8546
Cecilia Cueto-FelguerosoClinical Biochemistry Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
Laura RosiñolHematology Department, Hospital Clinic, Institut d'Investigacions Biomédiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain.
Albert OriolHospital Germans i Trials, Barcelona, Spain.
Ana Isabel TeruelHematology Department, Hospital Clínico de Valencia, Valencia, Spain.
Ana Lopez de la GuiaHematology Department, Hospital La Paz, Madrid, Spain.
Enrique BengoecheaHematology Department, Hospital de Donostia, San Sebastian, Spain.
Luis PalomeraHospital Clínico Universitario Lozano Blesa, Zaragoza, Spain.
Felipe de ArribaHospital Morales Meseguer, Murcia, Spain.
Jose Mariano HernandezHematology Department, Hospital General de Segovia, Segovia, Spain.
Miquel GranellHaematology, Hospital Univarsitari de la Santa Creu i Sant Pau, Barcelona,Spain.
Francisco Javier PeñalverHaematology Department, Hospital Universitario Fundacion Alcorcon, Madrid, Spain.
Ramon Garcia-SanzHematology Department, Hospital Universitario de Salamanca-IBSAL, IBMCC-CSIC, Salamanca, Spain.
Juan BesalduchHaematology Department, Hospital Univarsitari Son Espases, Mallorca, Spain.
Yolanda GonzalezHaematology Department, Institutd'Oncologia Dr Josep Trueta de Girona, Girona, Spain.
Rafael Benigno MartinezHaematology Department, Hospital Universitario San Carlos, Madrid, Spain.
Miguel Teodoro HernandezHaematology Department, Hospital Universitario de Canarias, Tenerife, Spain.
Norma C GutierrezHematology Department, Hospital Clinic, Institut d'Investigacions Biomédiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain.
Paloma PuertaClinical Biochemistry Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
Antonio ValeriHematology Department, Hospital Universitario 12 de Octubre, CIBERONC, Madrid, Spain.
Bruno PaivaHaematology Department, Clínica Universitaria de Navarra/ CIMA,IDISNA, CIBERONC,Pamplona, SPAIN.
Joan BladeHospital Germans i Trials, Barcelona, Spain.
Maria-Victoria MateosHematology Department, Hospital Clinic, Institut d'Investigacions Biomédiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain.
Jesus San MiguelHaematology Department, Clínica Universitaria de Navarra/ CIMA,IDISNA, CIBERONC,Pamplona, SPAIN.
Juan Jose LahuertaHematology Department, Hospital Universitario 12 de Octubre, CIBERONC, Madrid, Spain.
Joaquin Martinez-LopezHematology Department, Hospital Universitario 12 de Octubre, CIBERONC, Madrid, Spain.
GEM (Grupo Español de MM)/PETHEMA (Programa para el Estudio de la Terapéutica en Hemopatías Malignas) Cooperative Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated the prognostic impact and clinical utility of serum free light chains (sFLC) and serum heavy-light chains (sHLC) in patients with multiple myeloma treated according to the GEM2005MENOS65, GEM2005MAS65, and GEM2010MAS65 PETHEMA/GEM phase III clinical trials. Serum samples collected at diagnosis were retrospectively analyzed for sFLC (n = 623) and sHLC (n = 183). After induction or autologous transplantation, 309 and 89 samples respectively were available for sFLC and sHLC assays. At diagnosis, a highly abnormal (HA) sFLC ratio (sFLCr) (<0.03 or >32) was not associated with higher risk of progression. After therapy, persistence of involved-sFLC levels >100 mg/L implied worse survival (overall survival [OS], P = 0.03; progression-free survival [PFS], P = 0.007). Among patients that achieved a complete response, sFLCr normalization did not necessarily indicate a higher quality response. We conducted sHLC investigations for IgG and IgA MM. Absolute sHLC values were correlated with monoclonal protein levels measured with serum protein electrophoresis. At diagnosis, HA-sHLCrs (<0.29 or >73) showed a higher risk of progression (P = 0.006). Additionally, involved-sHLC levels >5 g/L after treatment were associated with shorter survival (OS, P = 0.001; PFS, P = 0.018). The HA-sHLCr could have prognostic value at diagnosis; absolute values of involved-sFLC >100 mg/L and involved-sHLC >5 g/L could have prognostic value after treatment.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsClinical Trials, Phase III as TopicHumansImmunoglobulin Heavy ChainsImmunoglobulin Light ChainsInduction ChemotherapyKaplan-Meier EstimateMultiple MyelomaPrognosisRetrospective StudiesStem Cell TransplantationTransplantation, AutologousImmunoglobulin Heavy ChainsImmunoglobulin Light Chains

Identifiers

PMID30192814
PMCPMC6128544

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Registered trials

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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.