Evidence map›Paper›PMID 37444475›Full record

ArticleCancers2023

Effect and Tolerance of N5 and N6 Chemotherapy Cycles in Combination with Dinutuximab Beta in Relapsed High-Risk Neuroblastoma Patients Who Failed at Least One Second-Line Therapy.

Holger N Lode, Ruth Ladenstein, Sascha Troschke-Meurer, Linda Struppe, Nikolai Siebert, Maxi Zumpe, Karoline Ehlert, Stefanie Huber, Evgenia Glogova, Patrick Hundsdoerfer and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

14 authors at 5 institutions in 4 countries.

Holger N LodeDepartment of Pediatric Hematology and Oncology, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0002-1201-208X
Ruth LadensteinDepartment of Paediatrics, St. Anna Children's Hospital, Medical University of Vienna, 1090 Vienna, Austria.
Sascha Troschke-MeurerDepartment of Pediatric Hematology and Oncology, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0002-6185-462X
Linda StruppeDepartment of Pediatric Hematology and Oncology, University Medicine Greifswald, 17475 Greifswald, Germany.
Nikolai SiebertDepartment of Pediatric Hematology and Oncology, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0001-6254-1302
Maxi ZumpeDepartment of Pediatric Hematology and Oncology, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0003-0297-6739
Karoline EhlertDepartment of Pediatric Hematology and Oncology, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0003-2992-5376
Stefanie HuberDepartment of Pediatric Hematology and Oncology, University Medicine Greifswald, 17475 Greifswald, Germany.
Evgenia GlogovaDepartment of Paediatrics, St. Anna Children's Hospital, Medical University of Vienna, 1090 Vienna, Austria.
Patrick HundsdoerferHelios Klinikum Berlin Buch, 13125 Berlin, Germany.
Angelika EggertClinic for Pediatric Hematology and Oncology, Charité University Medicine Berlin, 13353 Berlin, Germany.ORCID 0000-0003-3476-8184
Anna Zaniewska-TekieliDepartment of Pediatric Oncology and Hematology, Jagiellonian University Medical College, 31-008 Krakow, Poland.
Walentyna BalwierzDepartment of Pediatric Oncology and Hematology, Jagiellonian University Medical College, 31-008 Krakow, Poland.ORCID 0000-0002-5379-2318
Aleksandra WieczorekDepartment of Pediatric Oncology and Hematology, Jagiellonian University Medical College, 31-008 Krakow, Poland.ORCID 0000-0001-6750-2628
Universitätsmedizin Greifswald · DEJagiellonian University · PLSt Anna Children's Hospital · ATCharité - Universitätsmedizin Berlin · DEHelios Hospital Berlin-Buch · DE

Funding

Deutsche Forschungsgemeinschaft (DFG) SI 2147Hector Stiftungen, Germany M2116University Medicine Greifswald 97237000
6 · The paper itself

Abstract

The anti-disialoganglioside (GD2) monoclonal antibody dinutuximab beta is approved for the maintenance treatment of high-risk neuroblastoma. Dinutuximab beta combined with different chemotherapy regimens is being investigated in various clinical settings. We conducted a retrospective clinical chart review of 25 patients with relapsed/refractory neuroblastoma who had failed ≥1 second-line therapy and received compassionate use treatment with dinutuximab beta long-term infusion combined with the induction chemotherapy regimens N5 (cisplatin, etoposide, vindesine) and N6 (vincristine, dacarbazine, ifosfamide, doxorubicin) recommended by the German Pediatric Oncology and Hematology Group [GPOH] guidelines. The treatment did not result in any unexpected severe toxicities or in any major treatment delays. Grade 3/4 pain was reported by 4/25 patients in cycle 1, decreasing to 0/9 patients in cycles 3 and 4. The median follow-up was 0.6 years. The best response in this group was 48% (12/25 patients), which included three patients with minor responses. At 1 year, the estimated event-free survival was 27% (95% confidence interval [CI] 8-47) and overall survival was 44% (95% CI 24-65). Combining long-term infusion of dinutuximab beta with N5 and N6 chemotherapy demonstrated an acceptable safety profile and encouraging objective response rates in heavily pretreated patients with high-risk neuroblastoma, warranting further evaluation in clinical trials.

Indexed as

chemoimmunotherapydinutuximab betaganglioside GD2neuroblastomarefractoryrelapsed

Identifiers

PMID37444475
PMCPMC10341209
OpenAlexW4382402620

What OpenQuestion holds

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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.