Evidence map›Paper›PMID 35385885›Full record

ArticleHematological oncology2022

Does early disease progression predict survival after first line-treatment of Waldenström macroglobulinemia?

Julien Labreuche, Deborah Assouan, Eric Durot, Cecile Tomowiak, Damien Roos-Weil, Elise Toussaint, Fontanet Bijou, Richard Lemal, Annie Brion, Kamel Laribi and 4 more

Abstract read
In one paragraph

Article in Hematological oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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  5. 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

14 authors.

Julien LabreucheUniversite de Lille, CHU Lille, ULR 2694-METRICS: évaluation des technologies de santé et des pratiques médicales, Lille, France.
Deborah AssouanService d'Hematologie Clinique et Therapie Cellulaire, Centre Hospitalier Universitaire d'Amiens-Picardie, Amiens, France.
Eric DurotService d'Hématologie Clinique, Hôpital Robert Debré, Centre Hospitalier Universitaire de Reims, Reims, France.ORCID https://orcid.org/0000-0003-3463-0089
Cecile TomowiakService d'Oncologie Hématologie et Thérapie cellulaire, CHU de Poitiers, Poitiers, France.
Damien Roos-WeilHôpital Pitié Salpêtrière APHP GRC-11 UPMC, Paris, France.
Elise ToussaintDepartement d'Hematologie, CHU de Strasbourg, Strasbourg, France.
Fontanet BijouDepartement d'Hematologie, Institut Bergonié, Bordeaux, France.
Richard LemalService d'Hematologie Clinique Adultes de Thérapie Cellulaire, Hôpital Estaing, Université d'Auvergne EA7283, Inserm CIC-501, CHU Clermont-Ferrand, Clermont Ferrand, France.
Annie BrionDepartement d'Hematologie, CHRU de Besançon, Besançon, France.
Kamel LaribiDepartement d'Hematologie, Centre Hospitalier du Mans, Le Mans, France.ORCID https://orcid.org/0000-0002-4389-6164
Loic YsebaertService d'Hématologie IUC Toulouse-Oncopole Toulouse, Toulouse, France.
Alain DuhamelUniversite de Lille, CHU Lille, ULR 2694-METRICS: évaluation des technologies de santé et des pratiques médicales, Lille, France.
Pierre MorelUniversite de Lille, CHU Lille, ULR 2694-METRICS: évaluation des technologies de santé et des pratiques médicales, Lille, France.ORCID https://orcid.org/0000-0002-0782-3144
French Innovative Leukaemia Organisation (FILO) Chronic Lymphocytic Leukaemia group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In symptomatic Waldenström macroglobulinemia (sWM) patients, prognosis is assessed with the international prognostic scoring system (IPSSWM). In follicular lymphoma and other B-cell and T-cell lymphomas, disease progression within 24 months (POD24) or (in patients without POD24) after 24 months has been proposed as the start date for stratifying subsequent survival. In the present report, we assessed in a large series of 472 sWM patients, the prognostic value of this new dynamic endpoint already reported in many other lymphomas subtypes. The 3 year subsequent survival for patients with POD24 was 75% and 93% for patients without POD24. In sWM patients, departure from the proportional hazards assumption complicated this analysis. In patients without POD24, the median subsequent progression-free survival time of 43 months accounted for favorable outcome, whereas survival after progression was not influenced by the time to progression. In addition, sensitivity analysis showed that the baseline IPSSWM score also influenced survival after POD24. In sWM patients, we conclude that the apparent difference in survival after POD24 or the 24 months time-point (in patients without POD24) is mainly explained by the prolonged subsequent progression free survival of latter patients. Indeed, the mortality after progression is not influenced by the time to this event.

Indexed as

Disease ProgressionWaldenstrom MacroglobulinemiaHumansPrognosisProgression-Free SurvivalprogressionsurvivalWaldenström macroglobulinemia

Identifiers

PMID35385885
PMCPMC9541850

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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.