Evidence map›Paper›PMID 37195291›Full record

ArticleAnnals of hematology2023

Therapy results in pediatric Hodgkin lymphoma - does less mean better? Experience from a single children's oncology center.

Joanna Stankiewicz, Andrzej Kołtan, Ewa Demidowicz, Natalia Bartoszewicz, Sylwia Kołtan, Krzysztof Czyżewski, Monika Richert-Przygońska, Robert Dębski, Monika Pogorzała, Barbara Tejza and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Annals of hematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

22 authors at 1 institution in 1 country.

Joanna StankiewiczDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland. joanna.konieczek@cm.umk.pl.ORCID http://orcid.org/0000-0001-7419-1936
Andrzej KołtanDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Ewa DemidowiczDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Natalia BartoszewiczDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Sylwia KołtanDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Krzysztof CzyżewskiDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Monika Richert-PrzygońskaDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Robert DębskiDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Monika PogorzałaDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Barbara TejzaDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Joanna CisekDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Piotr KsiężniakiewiczDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Agnieszka Jatczak-GacaDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Agata MarjańskaDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Marlena SalamonDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Anna DąbrowskaDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Anna UrbańczykDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Elżbieta GrześkDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Kamila JaremekDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Monika ŁęckaDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Oliwia GrochowskaDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Jan StyczyńskiDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Toruń, Antoni Jurasz University Hospital No.1, Ul. Sklodowskiej-Curie 9, 85-094, Bydgoszcz, Poland.
Nicolaus Copernicus University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapy results in pediatric Hodgkin lymphoma reflect remarkable progress in pediatric oncology. In the last decade, relevant development of new therapeutic options for children with refractory or relapsed disease has been made. In this study, we retrospectively analyzed therapy results and risk factors in children treated in a single oncology center according to five therapeutic protocols. Data from 114 children treated by a single institution between 1997 and 2022 were analyzed. Classic Hodgkin lymphoma therapy results were divided into four therapeutic periods: 1997-2009, 2009-2014, 2014-2019, and 2019-2022. For nodular lymphocyte-predominant Hodgkin lymphoma, data from one therapeutic protocol was analyzed. For the entire group, the 5-year probability of overall survival was 93.5%. There were no statistically significant differences between therapeutic periods. The occurrence of B symptoms at diagnosis and incidence of relapse were risk factors for death (p = 0.018 and p < 0.001). Relapse occurred in 5 cases. The 5-year probability of relapse-free survival for the entire group was 95.2%, without significant differences between groups. Patients treated between 1997 and 2009 had over a sixfold higher risk for events, defined as primary progression, relapse, death, or incidence of secondary malignancies (OR = 6.25, p = 0.086). The 5-year probability of event-free survival for all patients was 91.3%. Five patients died, and the most common cause of death was relapse. Modern therapeutic protocols in pediatric Hodgkin lymphoma are marked by excellent outcomes. Patients with disease relapses have a notably high risk of death, and the development of new therapeutic options for this group remains one of the main goals of current trials.

Indexed as

Hodgkin DiseaseAntineoplastic Combined Chemotherapy ProtocolsChildDisease-Free SurvivalHumansNeoplasm Recurrence, LocalRetrospective StudiesChildrenHodgkin lymphomaRadiotherapySurvivalTherapeutic era

Identifiers

PMID37195291
PMCPMC10345031
OpenAlexW4376871545

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.