Evidence map›Paper›PMID 27121472›Full record

ArticleBlood2016

Dasatinib and low-intensity chemotherapy in elderly patients with Philadelphia chromosome-positive ALL.

Philippe Rousselot, Marie Magdelaine Coudé, Nicola Gokbuget, Carlo Gambacorti Passerini, Sandrine Hayette, Jean-Michel Cayuela, Françoise Huguet, Thibaut Leguay, Patrice Chevallier, Celia Salanoubat and 27 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 152 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
152citing papers in PubMed, 3 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.

NCT04554459 phase2terminatednot on this mapstarted 2021, after this paper: background citation

Ponatinib Plus Reduced-intensity Chemotherapy in the First-line Treatment of Adult Patients With Ph-positive Acute Lymphoblastic Leukemia

TypeinterventionalSponsorInstitute of Hematology and Blood Transfusion, Czech RepublicRan2021 to 2024Enrolled4ConditionsAcute Lymphoblastic Leukemia, Adult, Ph+ ALL, Newly DiagnosedArmsPonatinib 15 MG Oral Tablet
NCT06175702 not yet recruitingnot on this mapstarted 2023, after this paper: background citation

Treatment Protocol for Newky Diagnosed Adult Ph-Chromosome Positive (BCR::ABL1) Acute Lymphoblastic Leukemia (LALPh2022)

TypeobservationalSponsorPETHEMA FoundationRan2023 to 2030Enrolled150ConditionsLymphoblastic Leukemia, Philadelphia-Positive ALL, Adult ALLArmsVincristine, Dexamethasone, Imatinib, Cytarabine, Mercaptopurine
3 · Its place in the literature

Who cites it

152 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  9. Reconsidering dualTranslational cancer research · 2026
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  18. How I treat Ph+ acute lymphoblastic leukemia.Future oncology (London, England) · 2025
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92 more citing papers are in PubMed but not listed here.

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

37 authors.

Philippe RousselotHemato-Oncology Unit, Centre Hospitalier de Versailles, Le Chesnay, France; Université Versailles Saint Quentin en Yvelines, EA4340, Université Paris-Saclay, Communauté Paris-Saclay, France;ORCID 0000-0003-3238-4494
Marie Magdelaine CoudéLaboratory of Hematology, University Hospital Saint-Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France; EA3518, University Paris Diderot, Paris, France;
Nicola GokbugetMedicine Department II, Johann Wolfgang Goethe Universität, Frankfurt, Germany;
Carlo Gambacorti PasseriniDepartment of Internal Medicine/Experimental Oncology, University of Milano Bicocca, Monza, Italy;
Sandrine HayetteDivision of Hematology, Hospices Civils de Lyon, INSERM U1052-Centre National de la Recherche Scientifique UMR 5286, Centre Hospitalier Lyon Sud, Pierre Bénite, France;
Jean-Michel CayuelaLaboratory of Hematology, University Hospital Saint-Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France; EA3518, University Paris Diderot, Paris, France;
Françoise HuguetDivision of Hematology, Institut Universitaire de Cancérologie, Toulouse, France;
Thibaut LeguayDivision of Hematology, Hôpital du Haut-Levêque, Pessac, France;
Patrice ChevallierHematology Department, CHU Hotel-Dieu, Nantes, France;
Celia SalanoubatDivision of Hematology, Centre Hospitalier Sud Francilien, Corbeil Essonne, France;
Caroline BonmatiDivision of Hematology, Hôpital de Brabois, Centre Hospitalier Universitaire de Nancy, Nancy, France;
Magda AlexisService d'Oncologie et d'Hématologie, Hôpital de la Source, Orléans, France;
Mathilde HunaultDivision of Hematology, Centre Hospitalier Universitaire d'Angers, Angers, France; INSERM U892/Centre National de la Recherche Scientifique 6299, Angers, France;
Sylvie GlaisnerDivision of Hematology, Institut Curie-Hôpital Rene Huguenin, Saint-Cloud, France;
Philippe AgapeDivision of Hematology, Centre Hospitalier Départemental Felix Guyon, Saint Denis, La Réunion, France;
Christian BerthouDivision of Hematology, Centre Hospitalier Universitaire de Brest, Brest, France;
Eric JourdanDivision of Hematology, Centre Hospitalier Universitaire de Nîmes, Nîmes, France;
José FernandesDivision of Hematology, Hotel Dieu, Valenciennes, France;
Laurent SuttonDivision of Hematology, Centre Hospitalier Victor Dupouy, Argenteuil, France;
Anne BanosDivision of Hematology, Centre Hospitalier de la Côte Basque, Bayonne, France;
Oumedaly RemanDivision of Hematology, Centre Hospitalier Universitaire, Caen, France;
Bruno LioureDivision of Hematology, Hôpital de Hautepierre, Centre Hospitalier Universitaire de Strasbourg, Strasbourg, France;
Xavier ThomasDivision of Hematology, Hospices Civils de Lyon, INSERM U1052-Centre National de la Recherche Scientifique UMR 5286, Centre Hospitalier Lyon Sud, Pierre Bénite, France;
Norbert IfrahDivision of Hematology, Centre Hospitalier Universitaire d'Angers, Angers, France; INSERM U892/Centre National de la Recherche Scientifique 6299, Angers, France;
Marina Lafage-PochitaloffLaboratoire de Cytogénétique Onco-Hématologique, CHU Timone Enfants, Aix-Marseille University, Marseille, France;
Anne BornandService de Gériatrie Aigue Polyvalente and.
Laure MorissetDélégation à la Recherche Clinique et à l'Innovation, Hôpital Mignot, Le Chesnay, France;
Valérie RobinDivision of Hematology, CHR Mons-Hainaut, Mons, Belgium;
Heike PfeiferDepartment of Molecular Biology, Johann Wolfgang Goethe University, Frankfurt, Germany;
Andre DelannoyDépartement d'Hématologie, d'Oncologie Médicale et de Radiothérapie Oncologique, Centre Hospitalier de Jolimont-Lobbes, Haine Saint Paul, Belgium;
Josep RiberaDepartment of Clinical Hematology, ICO-Hospital Germans Trias i Pujol, Jose Carreras Research Institute, Badalona, Spain;
Renato BassanAzienda ULSS 12 "Veneziana" Direttore U.O.C. Ematologia, Venezia, Italy;
Marc DelordInstitut Universitaire d'Hématologie, Hôpital Saint-Louis, Paris, France;
Dieter HoelzerDepartment of Hematology, Johann Wolfgang Goethe University, Frankfurt, Germany;
Herve DombretDivision of Hematology, Hôpital Saint-Louis, AP-HP, University Paris Diderot, Paris, France; and.
Oliver G OttmannInstitute of Cancer & Genetics, Cardiff University School of Medicine, Cardiff, United Kingdom.ORCID 0000-0001-9559-1330
European Working Group on Adult ALL (EWALL) group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prognosis of Philadelphia-positive (Ph(+)) acute lymphoblastic leukemia (ALL) in the elderly has improved during the imatinib era. We investigated dasatinib, another potent tyrosine kinase inhibitor, in combination with low-intensity chemotherapy. Patients older than age 55 years were included in the European Working Group on Adult ALL (EWALL) study number 01 for Ph(+) ALL (EWALL-PH-01 international study) and were treated with dasatinib 140 mg/day (100 mg/day over 70 years) with intrathecal chemotherapy, vincristine, and dexamethasone during induction. Patients in complete remission continued consolidation with dasatinib, sequentially with cytarabine, asparaginase, and methotrexate for 6 months. Maintenance therapy was dasatinib and vincristine/dexamethasone reinductions for 18 months followed by dasatinib until relapse or death. Seventy-one patients with a median age of 69 years were enrolled; 77% had a high comorbidity score. Complete remission rate was 96% and 65% of patients achieved a 3-log reduction in BCR-ABL1 transcript levels during consolidation. Only 7 patients underwent allogeneic hematopoietic stem cell transplantation. At 5 years, overall survival was 36% and up to 45% taking into account deaths unrelated to disease or treatment as competitors. Thirty-six patients relapsed, 24 were tested for mutation by Sanger sequencing, and 75% were T315I-positive. BCR-ABL1(T315I) was tested by allele-specific oligonucleotide reverse transcription-quantitative polymerase chain reaction in 43 patients and detection was associated with short-term relapses. Ten patients (23%) were positive before any therapy and 8 relapsed, all with this mutation. In conclusion, dasatinib combined with low-intensity chemotherapy was well-tolerated and gave long-term survival in 36% of elderly patients with Ph(+) ALL. Monitoring of BCR-ABL1(T315I) from diagnosis identified patients with at high risk of early relapse and may help to personalize therapy.

Indexed as

AgedAged, 80 and overAntineoplastic AgentsDasatinibFemaleFusion Proteins, bcr-ablHumansMaleMiddle AgedMutationPhiladelphia ChromosomePrecursor Cell Lymphoblastic Leukemia-LymphomaPrognosisProspective StudiesProtein Kinase InhibitorsAntineoplastic AgentsBCR-ABL1 fusion protein, humanDasatinibFusion Proteins, bcr-ablProtein Kinase Inhibitors

Identifiers

PMID27121472
PMCPMC5085255

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Registered trials

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.