Evidence map›Paper›PMID 35865461›Full record

ArticleFrontiers in oncology2022

Long-Term Responders After Autologous Stem Cell Transplantation in Multiple Myeloma.

Aina Oliver-Caldes, Juan Carlos Soler-Perromat, Ester Lozano, David Moreno, Alex Bataller, Pablo Mozas, Marta Garrote, Xavier Setoain, Juan Ignacio Aróstegui, Jordi Yagüe and 8 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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

  1. The [European journal of nuclear medicine and molecular imaging · 2026
    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

18 authors.

Aina Oliver-CaldesHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
Juan Carlos Soler-PerromatRadiology Department Centre de Diagnòstic per la Imatge Clínic (CDIC), Hospital Clinic de Barcelona, Barcelona, Spain.
Ester LozanoInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
David MorenoHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
Alex BatallerHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
Pablo MozasHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
Marta GarroteHematopathology Unit, Pathology Department, Hospital Clinic de Barcelona, Barcelona, Spain.
Xavier SetoainNuclear Medicine Department, Hospital Clinic de Barcelona, Biomedical Imaging Group, Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Barcelona, Spain.
Juan Ignacio ArósteguiImmunology Department, Hospital Clinic de Barcelona, Barcelona, Spain.
Jordi YagüeImmunology Department, Hospital Clinic de Barcelona, Barcelona, Spain.
Natalia TovarHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
Raquel JiménezHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
Luis Gerardo Rodríguez-LobatoHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
M Teresa CibeiraHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
Laura RosiñolHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
Joan BladéHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
Manel JuanInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Carlos Fernández de LarreaHematology Department, Amyloidosis and Myeloma Unit, Hospital Clinic de Barcelona, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Multiple myeloma (MM) is considered an incurable hematological neoplasm. For transplant-eligible patients, initial treatment includes an induction phase followed by an autologous stem cell transplantation (ASCT). Despite the introduction of several drugs in the past years, relapses still occur. Nevertheless, some patients achieve sustained responses after successful induction treatment and ASCT. Methods: We retrospectively evaluated all patients diagnosed with MM in our institution who underwent induction treatment and ASCT between 1990 and 2015. The subset of patients who achieved a sustained response (any degree) for 5 or more years after ASCT without further treatment or signs of progression were distinguished as "long-term responders" (LTRs). In the non-LTR group, a cohort referred to as "prolonged responders" (PLRs) showed sustained response of at least 5 years after ASCT but eventually relapsed. We collected and analyzed clinical and laboratory data. Results: Two hundred and fifty patients were diagnosed with MM and received induction treatment and ASCT at our institution in the study period. Among them, 54 (21.6%) patients met the criteria for LTR. Some diagnostic features such as a younger age, female gender, ECOG performance status of 0, lower International Staging System (ISS) stage, lower bone marrow plasma cell infiltration, and lower serum levels of calcium, C-reactive protein, and lactate dehydrogenase (LDH) were found to be more prevalent in LTR. Female gender, an ECOG performance status of 0, a localized Durie-Salmon stage, an ISS of I-II, the absence of bone disease, and an LDH within normal range were also predictive of longer progression-free survival (PFS) and overall survival (OS) in the whole cohort. The depth of the response achieved after induction and ASCT as well as the administration of an IMID-based maintenance regimen may play a role in the differences observed on PFS between cohorts. A detectable M-protein with a monoclonal gammopathy of undetermined significance (MGUS)-like behavior was detected in one-third of LTR after ASCT. Although relapses continue to occur in patients who achieve a 5-year treatment-free period after ASCT, a plateau is observed in the survival curves at approximately 21 years of follow-up.

Indexed as

autologous stem cell transplantationlong-term respondersmultiple myelomaoligoclonal bandspositron emission tomography/computed tomographyT cell clones

Identifiers

PMID35865461
PMCPMC9294166

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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.