Evidence map›Paper›PMID 37216396›Full record

ArticleBlood advances2023

Vemurafenib combined with cladribine and cytarabine results in durable remission of pediatric BRAF V600E-positive LCH.

Dmitry Evseev, Daria Osipova, Irina Kalinina, Elena Raykina, Anna Ignatova, Evelina Lyudovskikh, Dina Baidildina, Alexander Popov, Vladimir Zhogov, Alexandra Semchenkova and 15 more

3 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.6field-weighted citation impact, top 4% 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.

NCT03585686 phase2unknown statusnot on this map

The Prospective Non-randomized Phase II Clinical Trial of Vemurafenib in Combination With Cytarabine and 2-chlorodeoxyadenosine in Children With Langerhans-cell Hisitocytosis With BRAF V600E Mutation

TypeinterventionalSponsorFederal Research Institute of Pediatric Hematology, Oncology and ImmunologyRan2018 to 2023Enrolled12ConditionsLangerhans Cell HistiocytosisArmsVemurafenib, Cytarabine, 2-chlorodeoxyadenosine
NCT07022834 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

A Real-world Investigation of the Combination of Darafenib or Trametinib and Clofarabine in the Treatment of High-risk, Recurrent, or Refractory Pediatric Patients With Langerhans Cell Histiocytosis.

TypeinterventionalSponsorWest China Second University HospitalRan2025 to 2030Enrolled20ConditionsLangerhans Cell Histiocytosis (LCH)ArmsDabrafenib or Trametinib and Clofarabine
NCT07431060 narecruitingnot on this mapstarted 2026, after this paper: background citation

Modified LCH-III Regimen Versus Modified LCH-III Regimen Combined With Luvometinib in the Treatment of Multisystem Pediatric Langerhans Cell Histiocytosis: A Multicenter, Open-Label, Randomized Controlled Clinical Trial

TypeinterventionalSponsorWest China Second University HospitalRan2026 to 2030Enrolled120ConditionsLangerhans Cell Histiocytosis (LCH)ArmsPrednisone, Vincristine, Mercaptopurine, Luvometinib
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
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  5. Observational
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  7. Cell-free BRAFHaematologica · 2026
    Article
  8. Article
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  11. Review
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  13. Article
  14. A clinical study incorporating multimodalFrontiers in medicine · 2025
    Article
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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

25 authors at 2 institutions in 1 country.

Dmitry EvseevDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.ORCID 0000-0001-8610-0624
Daria OsipovaDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.ORCID 0000-0002-9968-9332
Irina KalininaDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Elena RaykinaDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Anna IgnatovaDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Evelina LyudovskikhDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.ORCID 0000-0003-0717-2019
Dina BaidildinaDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Alexander PopovDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.ORCID 0000-0002-0889-6986
Vladimir ZhogovDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Alexandra SemchenkovaDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.ORCID 0000-0002-7082-1694
Eugeny LitvinDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.ORCID 0000-0002-6331-5339
Natalia KotskayaDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Ekaterina CherniakDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.ORCID 0000-0002-3852-9634
Kirill VoroninDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Eugeny BurtsevHematopoietic Stem Cell Transplantation Department, Morozov Children Hospital, Moscow, Russia.ORCID 0000-0002-3623-6547
Gleb BroninHematopoietic Stem Cell Transplantation Department, Morozov Children Hospital, Moscow, Russia.ORCID 0000-0002-0694-3996
Irina VlasovaHematopoietic Stem Cell Transplantation Department, Morozov Children Hospital, Moscow, Russia.ORCID 0000-0002-9209-7238
Bazarma PurbuevaHematology and Chemotherapy Department №1, Russian Children's Clinical Hospital, Moscow, Russia.
Olesya FinkHematology and Chemotherapy Department №1, Russian Children's Clinical Hospital, Moscow, Russia.ORCID 0000-0003-1336-9379
Ekaterina PristanskovaHematology and Chemotherapy Department №1, Russian Children's Clinical Hospital, Moscow, Russia.ORCID 0000-0002-4569-657X
Irina DzhukaevaPediatric Hematology and Oncology Department, Piotrovich Regional Children Clinical Hospital, Khabarovsk, Russia.
Elena EregaPediatric Hematology and Oncology Department, Piotrovich Regional Children Clinical Hospital, Khabarovsk, Russia.
Galina NovichkovaDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Alexey MaschanDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.ORCID 0000-0002-0016-6698
Michael MaschanDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.ORCID 0000-0003-1735-0093
Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology · RURussian Children's Clinical Hospital · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Langerhans cell histiocytosis (LCH) is a disorder with a variety of clinical signs. The most severe forms affect risk organs (RO). The established role of the BRAF V600E mutation in LCH led to a targeted approach. However, targeted therapy cannot cure the disease, and cessation leads to quick relapses. Here, we combined cytosine-arabinoside (Ara-C) and 2'-chlorodeoxyadenosine (2-CdA) with targeted therapy to achieve stable remission. Nineteen children were enrolled in the study: 13 were RO-positive (RO+) and 6 RO-negative (RO-). Five patients received the therapy upfront, whereas the other 14 received it as a second or third line. The protocol starts with 28 days of vemurafenib (20 mg/kg), which is followed by 3 courses of Ara-C and 2-CdA (100 mg/m2 every 12 h, 6 mg/m2 per day, days 1-5) with concomitant vemurafenib therapy. After that, vemurafenib therapy was stopped, and 3 courses of mono 2-CdA followed. All patients rapidly responded to vemurafenib: the median disease activity score decreased from 13 to 2 points in the RO+ group and from 4.5 to 0 points in the RO- group on day 28. All patients except 1 received complete protocol treatment, and 15 of them did not have disease progression. The 2-year reactivation/progression-free survival (RFS) for RO+ was 76.9% with a median follow-up of 21 months and 83.3% with a median follow-up of 29 months for RO-. Overall survival is 100%. Importantly, 1 patient experienced secondary myelodysplastic syndrome after 14 months from vemurafenib cessation. Our study demonstrates that combined vemurafenib plus 2-CdA and Ara-C is effective in a cohort of children with LCH, and the toxicity is manageable. This trial is registered at www.clinicaltrials.gov as NCT03585686.

Indexed as

CladribineHistiocytosis, Langerhans-CellChildCytarabineHumansNeoplasm Recurrence, LocalProto-Oncogene Proteins B-rafVemurafenibBRAF protein, humanCladribineCytarabineProto-Oncogene Proteins B-rafVemurafenib

Identifiers

PMID37216396
PMCPMC10500470
OpenAlexW4377294890

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.