Evidence map›Paper›PMID 30504932›Full record

ArticleBlood cancer journal2018

Feasibility of treatment discontinuation in chronic myeloid leukemia in clinical practice: results from a nationwide series of 236 patients.

Juan Carlos Hernández-Boluda, Arturo Pereira, Irene Pastor-Galán, Alberto Alvarez-Larrán, Alisa Savchuk, José Manuel Puerta, José María Sánchez-Pina, Rosa Collado, Alvaro Díaz-González, Anna Angona and 18 more

Abstract read
In one paragraph

Article in Blood cancer journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

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  19. The New ELN Recommendations for Treating CML.Journal of clinical medicine · 2020
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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

28 authors.

Juan Carlos Hernández-BoludaHematology Department, Hospital Clínico Universitario-INCLIVA, Valencia, Spain. hernandez_jca@gva.es.ORCID http://orcid.org/0000-0002-4289-3113
Arturo PereiraHemotherapy and Hemostasis Department, Hospital Clínic-IDIBAPS, Barcelona, Spain.
Irene Pastor-GalánHematology Department, Hospital Clínico Universitario-INCLIVA, Valencia, Spain.
Alberto Alvarez-LarránHematology Department, Hospital Clínic-IDIBAPS, University of Barcelona, Barcelona, Spain.
Alisa SavchukHematology Department, Hospital Universitario La Princesa, Madrid, Spain.
José Manuel PuertaHematology Department, Hospital Universitario Virgen de las Nieves, Granada, Spain.
José María Sánchez-PinaHematology Department, Hospital 12 de Octubre, Madrid, Spain.
Rosa ColladoHematology Department, Hospital General Universitario, Valencia, Spain.
Alvaro Díaz-GonzálezHematology Department, Hospital La Fe, IIS La Fe, Valencia, Spain.
Anna AngonaHematology Department, Hospital del Mar-IMIM, Barcelona, Spain.
Miguel SagüésHematology Department, Hospital Universitario de Girona, Doctor Josep Trueta, Girona, Spain.
Valentín García-GutiérrezHematology Department, Hospital Ramón y Cajal-IRYCIS, Madrid, Spain.
Concepción BoquéHematology Department, Institut Català d'Oncologia, Hospital Duran i Reynals, Hospitalet de Llobregat, Spain.
Santiago OsorioHematology Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Rolando VallansotHematology Department, Hospital Universitario Joan XXIII, Tarragona, Spain.
Luis PalomeraHematology Department, Hospital Clínico Universitario Lozano Blesa, IIS Aragón, Zaragoza, Spain.
Arantxa MendizábalHematology Department, Hospital Universitario de Álava, Vitoria, Spain.
Luis Felipe CasadoHematology Department, Hospital Virgen de la Salud, Toledo, Spain.
Manuel Pérez-EncinasHematology Department, Hospital Clínico Universitario, Santiago de Compostela, Spain.
Raúl Pérez-LópezHematology Department, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.
Francisca Ferrer-MarínHematology and Medical Oncology Department, Hospital Morales Meseguer-CIBERER, IMIB-Arrixaca, UCAM, Murcia, Spain.
Fermín Sánchez-GuijoHematology Department, Hospital Universitario de Salamanca, IBSAL, Salamanca, Spain.
Carmen GarcíaHematology Department, Hospital General Universitario de Alicante, Alicante, Spain.
Natalia de Las HerasHematology Department, Complejo Asistencial Universitario de León, León, Spain.
José Luis López-LorenzoHematology Department, Fundación Jiménez Díaz, Madrid, Spain.
Francisco CervantesHematology Department, Hospital Clínic-IDIBAPS, University of Barcelona, Barcelona, Spain.
Juan Luis SteegmannHematology Department, Hospital Universitario La Princesa, Madrid, Spain.
Grupo Español de Leucemia Mieloide Crónica (GELMC)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over half of chronic myeloid leukemia (CML) patients in deep molecular response do not lose the major molecular response (MMR) after stopping treatment with tyrosine kinase inhibitors (TKI). This strategy is safe in clinical trials, but its applicability in the real-life setting remains unsettled. We describe the outcomes after TKI discontinuation in a nationwide series of 236 CML patients. Median follow-up from treatment discontinuation was 21.5 months and 5 patients died from CML-unrelated causes. TKI therapy was reinitiated due to MMR loss (n = 52), increase ≥ 1 log in BCR-ABL transcript level without losing MMR (n = 12), patient preference (n = 2), and withdrawal syndrome (n = 1). Treatment-free remission rate at 4 years was 64% (95% confidence interval, CI: 55%-72%). Cumulative incidence of molecular recurrence at 3 years was 33% (95% CI: 26%-38%). TKI treatment for < 5 years and MR4.5 duration shorter than 4 years were both associated with higher incidence of molecular recurrence. No patient had disease progression. Response status at last control was: MR4.5 (n = 196), MR4 (n = 15), MMR (n = 14), complete cytogenetic response (n = 10), and other (n = 1). A significant increase in Hb and cholesterol levels was observed after imatinib withdrawal. Our results demonstrate that TKI treatment discontinuation is feasible in real-life clinical practice.

Indexed as

AgedAnticarcinogenic AgentsBiomarkersDrug Resistance, NeoplasmFemaleFollow-Up StudiesFusion Proteins, bcr-ablHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedProportional Hazards ModelsProtein Kinase InhibitorsRecurrenceTreatment OutcomeAnticarcinogenic AgentsBiomarkersFusion Proteins, bcr-ablProtein Kinase Inhibitors

Identifiers

PMID30504932
PMCPMC6275158

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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.