Evidence map›Paper›PMID 27748046›Full record

ArticleCancer medicine2016

Clofarabine versus fludarabine-based reduced-intensity conditioning regimen prior to allogeneic transplantation in adults with AML/MDS.

Patrice Chevallier, Myriam Labopin, Regis Peffault de La Tour, Bruno Lioure, Claude-Eric Bulabois, Anne Huynh, Didier Blaise, Pascal Turlure, Etienne Daguindau, Natacha Maillard and 14 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Cancer medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 15% 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.

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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Observational
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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

24 authors at 18 institutions in 2 countries.

Patrice ChevallierHematology Department, CHU Hotel-Dieu, Nantes, France.
Myriam LabopinUniversité Pierre & Marie Curie, Paris, France.
Regis Peffault de La TourHematology Department, Hôpital Saint-Louis, Paris, France.
Bruno LioureHematology Department, CHRU Hautepierre, Strasbourg, France.
Claude-Eric BulaboisHematology Department, CHU, Grenoble, France.
Anne HuynhHematology Department, Centre Anti-cancéreux, Toulouse, France.
Didier BlaiseHematology Department, Institut Paoli-Calmette, Marseille, France.
Pascal TurlureHematology Department, CHU, Limoges, France.
Etienne DaguindauHematology Department, CHU, Besançon, France.
Natacha MaillardHematology Department, CHU, Poitiers, France.
Ibrahim Yakoub-AghaCHU de Lille, LIRIC INSERM U995, Université Lille2, Lille, France.
Gaelle GuillermHematology Department, CHU, Brest, France.
Jeremy DelageHematology Department, CHU, Montpellier, France.
Nathalie ContentinHematology Department, CHU, Rouen, France.
Jacques-Olivier BayHematology Department, CHU, Clermont-Ferrand, France.
Florence BeckerichHematology Department, CHU Henri Mondor, Creteil, France.
Jean-Henri BourhisHematology Department, IGR, Villejuif, France.
Marie DetraitHematology Department, CHU, Lyon, France.
Stéphane VigourouxHematology Department, CHU, Bordeaux, France.
Sylvie FrançoisHematology Department, CHU, Angers, France.
Faezeh LegrandHematology Department, CHU, Nice, France.
Thierry GuillaumeHematology Department, CHU Hotel-Dieu, Nantes, France.
Mohamad MohtyUniversité Pierre & Marie Curie, Paris, France.
SFGM-TC
Inserm · FRHotel Dieu Hospital · CACentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Limoges · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Nice · FRCentre Hospitalier Universitaire de Poitiers · FRCentre Hospitalier Universitaire de Rouen · FRCentre Hospitalier Universitaire Henri-Mondor · FRDélégation Ile-de-France Villejuif · FRHôpital Saint-Louis · FRHôpitaux Universitaires de Strasbourg · FRInstitut Paoli-Calmettes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have retrospectively compared survivals between acute myeloid leukemia (AML)/myelodysplastic syndrome (MDS) patients who received either a clofarabine/busulfan (CloB2A2) or a fludarabine/busulfan (FB2A2) RIC regimen for allogeneic stem cell transplantation. Between 2009 and 2014, 355 allotransplanted cases were identified from the SFGM-TC registry as having received either the FB2A2 (n = 316, 56% males, median age: 59.2 years, AML 78.5%, first complete remission [CR1] 72%, median follow-up: 20 months) or the CloB2A2 (n = 39, 62% males, median age: 60.8 years, AML 62%, CR1 69%, median follow-up: 22.4 months) RIC regimen. In multivariate analysis, FB2A2 was associated with significant lower overall survival (OS, HR: 2.14; 95%CI: 1.05-4.35, P = 0.04) and higher relapse incidence (RI, HR: 2.17; 95%CI: 1.02-4.61, P = 0.04) and a trend for lower leukemia-free survival (LFS, HR: 1.75; 95%CI: 0.94-3.26, P = 0.08). These results were confirmed using a propensity score-matching strategy. However, when considering AML and MDS patients separately, the benefit of the CLOB2A2 regimen was restricted to AML patients (2-year OS FB2A2: 38% [14.5-61.6] vs. CloB2A2: 79.2% [62.9-95.4], P = 0.01; 2-year LFS FB2A2: 38% [16-59.9] vs. CloB2A2: 70.8% [52.6-89], P = 0.03). The better survivals were due to the lower risk of relapse in this CloB2A2 AML subgroup (2-year RI FB2A2: 41.2% [19-62.4] vs. CloB2A2: 16.7% [5-34.2], P = 0.05). This retrospective comparison suggests that the CloB2A2 RIC regimen can likely provide longer survival than that awarded by a FB2A2 RIC regimen and may become a new standard of care RIC regimen for allotransplanted AML patients. A prospective phase 3 randomized study is warranted.

Indexed as

Hematopoietic Stem Cell TransplantationTransplantation ConditioningAdenine NucleotidesAdultAgedAntineoplastic Combined Chemotherapy ProtocolsArabinonucleosidesClofarabineFemaleFollow-Up StudiesHumansLeukemia, Myeloid, AcuteMaleMiddle AgedMyelodysplastic SyndromesRetrospective StudiesAdenine NucleotidesArabinonucleosidesClofarabinefludarabineVidarabineAcute myeloid leukemiaallogeneic stem cell transplantationclofarabinefludarabinemyelodysplastic syndromereduced-toxicity conditioning regimen

Identifiers

PMID27748046
PMCPMC5119961
OpenAlexW2537710036

What OpenQuestion holds

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LicenceCC BY
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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.