Evidence map›Paper›PMID 33322172›Full record

ArticleCancers2020

Clinical Outcome in Pediatric Patients with Philadelphia Chromosome Positive ALL Treated with Tyrosine Kinase Inhibitors Plus Chemotherapy-The Experience of a Polish Pediatric Leukemia and Lymphoma Study Group.

Joanna Zawitkowska, Monika Lejman, Marcin Płonowski, Joanna Bulsa, Tomasz Szczepański, Michał Romiszewski, Agnieszka Mizia-Malarz, Katarzyna Derwich, Grażyna Karolczyk, Tomasz Ociepa and 10 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. 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
0.7field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Resistance Mechanisms in Pediatric B-Cell Acute Lymphoblastic Leukemia.International journal of molecular sciences · 2022
    Review
  4. Review
  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

20 authors at 12 institutions in 1 country.

Joanna ZawitkowskaDepartment of Pediatric Hematology, Oncology and Transplantology, Medical University of Lublin, 20-059 Lublin, Poland.ORCID 0000-0001-7207-156X
Monika LejmanLaboratory of Genetic Diagnostics, Medical University of Lublin, 20-059 Lublin, Poland.ORCID 0000-0002-8760-0775
Marcin PłonowskiDepartment of Pediatric Oncology, Hematology, Medical University of Bialystok, 15-089 Bialystok, Poland.
Joanna BulsaDepartment of Pediatrics, Hematology and Oncology, Medical University of Silesia, 40-752 Katowice, Poland.
Tomasz SzczepańskiDepartment of Pediatrics, Hematology and Oncology, Medical University of Silesia, 40-752 Katowice, Poland.ORCID 0000-0001-5336-261X
Michał RomiszewskiDepartment of Hematology and Pediatrics, Medical University of Warsaw, 02-091 Warsaw, Poland.
Agnieszka Mizia-MalarzDepartment of Pediatric Oncology, Hematology and Chemotherapy, Medical University of Silesia, 40-752 Katowice, Poland.
Katarzyna DerwichDepartment of Pediatric Oncology, Hematology and Transplantology, Poznan University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0001-7239-4035
Grażyna KarolczykDepartment of Pediatric Oncology and Hematology, School of Medicine Jan Kochanowski University, 25-317 Kielce, Poland.
Tomasz OciepaDepartment of Pediatrics, Hematology and Oncology, Pomeranian Medical University of Szczecin, 70-204 Szczecin, Poland.
Magdalena ĆwiklińskaDepartment of Pediatric Oncology and Hematology, Jagiellonian University Medical College, 31-008 Krakow, Poland.
Joanna TrelińskaDepartment of Pediatrics, Oncology & Hematology, Medical University of Lodz, 90-647 Lodz, Poland.
Joanna Owoc-LempachDepartment of Pediatric Transplantology, Oncology, Hematology, Wroclaw Medical University, 50-367 Wroclaw, Poland.
Ninela Irga-JaworskaDepartment of Pediatrics, Hematology, Oncology and Endocrinology, Medical University of Gdansk, 80-210 Gdansk, Poland.
Anna MałeckaDepartment of Pediatrics, Hematology, Oncology and Endocrinology, Medical University of Gdansk, 80-210 Gdansk, Poland.
Katarzyna MachnikJohn Paul II Upper Silesian Child Health Centre, Department of Pediatric Hematology and Oncology, Medical University of Silesia, 40-752 Katowice, Poland.
Justyna Urbańska-RakusJohn Paul II Upper Silesian Child Health Centre, Department of Pediatric Hematology and Oncology, Medical University of Silesia, 40-752 Katowice, Poland.
Radosław ChaberClinic of Pediatric Oncology and Hematology, Faculty of Medicine, University of Rzeszow, 35-959 Rzeszow, Poland.ORCID 0000-0002-6862-9142
Jerzy KowalczykDepartment of Pediatric Hematology, Oncology and Transplantology, Medical University of Lublin, 20-059 Lublin, Poland.
Wojciech MłynarskiDepartment of Pediatrics, Oncology & Hematology, Medical University of Lodz, 90-647 Lodz, Poland.ORCID 0000-0003-2714-5851
Medical University of Silesia · PLMedical University of Lublin · PLGdańsk Medical University · PLMedical University of Lodz · PLJagiellonian University · PLJan Kochanowski University · PLMedical University of Białystok · PLMedical University of Warsaw · PLPoznan University of Medical Sciences · PLUniversity of Rzeszów · PLUniversity of Szczecin · PLWroclaw Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment of children with Philadelphia chromosome positive acute lymphoblastic leukemia (ALL Ph+) is currently unsuccessful. The use of tyrosine kinase inhibitors (TKIs) combined with chemotherapy has modernized ALL Ph+ therapy and appears to improve clinical outcome. We report herein the toxicity events and results of children with ALL Ph+ treated according to the EsPhALL2010 protocol (the European intergroup study of post-induction treatment of Philadelphia chromosome positive ALL) in 15 hemato-oncological centers in Poland between the years 2012 and 2019. The study group included 31 patients, aged 1-18 years, with newly diagnosed ALL Ph+. All patients received TKIs. Imatinib was used in 30 patients, and ponatinib was applied in one child due to T315I and M244V mutation. During therapy, imatinib was replaced with dasatinib in three children. The overall survival of children with ALL Ph+ treated according to the EsPhALL2010 protocol was 74.1% and event-free survival was 54.2% after five years. The cumulative death risk of the study group at five years was estimated at 25.9%, and its cumulative relapse risk was 30%. Our treatment outcomes are still disappointing compared to other reports. Improvements in supportive care and emphasis placed on the determination of minimal residual disease at successive time points, which will impact decisions on therapy, may be required.

Indexed as

ALL Ph+childrenoutcometoxicitytyrosine kinase inhibitors (TKIs)

Identifiers

PMID33322172
PMCPMC7763070
OpenAlexW3112747035

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.