Evidence map›Paper›PMID 28532436›Full record

ArticleOrphanet journal of rare diseases2017

Vinblastine chemotherapy in adult patients with langerhans cell histiocytosis: a multicenter retrospective study.

Abdellatif Tazi, Gwenaël Lorillon, Julien Haroche, Antoine Neel, Stéphane Dominique, Achille Aouba, Jean-David Bouaziz, Constance de Margerie-Melon, Emmanuelle Bugnet, Vincent Cottin and 5 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Orphanet journal of rare diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Role ofQuantitative imaging in medicine and surgery · 2022
    Article
  9. Article
  10. Adult Langerhans Cell Histiocytosis and the Skeleton.Journal of clinical medicine · 2022
    Review
  11. Article
  12. Histiocytic disorders.Nature reviews. Disease primers · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Paediatric pulmonary Langerhans cell histiocytosis.Breathe (Sheffield, England) · 2020
    Review
  20. Review
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

15 authors at 10 institutions in 1 country.

Abdellatif TaziAssistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis, Centre National de Référence de l'Histiocytose Langerhansienne, Service de Pneumologie, 1 Avenue Claude Vellefaux, 75475, Paris Cedex 10, France. abdellatif.tazi@aphp.fr.ORCID 0000-0003-0788-7444
Gwenaël LorillonAssistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis, Centre National de Référence de l'Histiocytose Langerhansienne, Service de Pneumologie, 1 Avenue Claude Vellefaux, 75475, Paris Cedex 10, France.
Julien HarocheAssistance Publique-Hôpitaux de Paris, Hôpital Pitié Salpêtrière, Service de Médecine Interne, Université Pierre et Marie Curie, Paris, France.
Antoine NeelCHU de Nantes, Hôpital Hôtel Dieu, Service de Médecine Interne, Nantes, France.
Stéphane DominiqueDépartement de Pneumologie, Hôpital Charles Nicolle, Rouen, France.
Achille AoubaAssistance Publique-Hôpitaux de Paris, Hôpital Cochin, Service de Médecine Interne, Paris, France.
Jean-David BouazizAssistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis, Département de Dermatologie, Univ Paris Diderot, Sorbonne Paris Cité, Inserm U976, Paris, France.
Constance de Margerie-MelonAssistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis, Service de Radiologie, Paris, France.
Emmanuelle BugnetAssistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis, Centre National de Référence de l'Histiocytose Langerhansienne, Service de Pneumologie, 1 Avenue Claude Vellefaux, 75475, Paris Cedex 10, France.
Vincent CottinGroupement Hospitalier Est, Service de Pneumologie, Université Claude Bernard Lyon 1, Lyon, France.
Thibault ComontInstitut Universitaire du Cancer de Toulouse-Oncopôle, CHU de Toulouse, Service de Médecine Interne, Toulouse, France.
Christian LavigneCHU Angers, Service de Médecine Interne et vasculaire, Angers, France.
Jean-Emmanuel KahnUniversité Saint-Quentin en Yvelines, Hôpital Foch, Service de Médecine Interne, Suresnes, France.
Jean DonadieuAssistance Publique-Hôpitaux de Paris, Hôpital Trousseau, Centre National de Référence de l'Histiocytose Langerhansienne, Service d'Hémato-Oncologie pédiatrique, Paris, France.
Sylvie ChevretUniversité Paris Diderot, Sorbonne Paris Cité, Inserm UMR-1153 (CRESS), Biostatistics and Clinical Epidemiology research team (ECSTRA), Paris, France.
Assistance Publique – Hôpitaux de Paris · FRInserm · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Toulouse · FRHôpital Charles-Nicolle · FRHôpital Cochin · FRHôpital Foch · FRSorbonne Université · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVinblastine is the standard treatment for children with Langerhans cell histiocytosis (LCH). Whether this treatment could be extended to adults with LCH is questionable. This retrospective multicenter study included 35 adult patients (median age 33 years; 23 men; 80% with multisystem LCH) who were treated with vinblastine + steroids as a first-line chemotherapy and followed for a median time of 83 months. The objectives were to determine the overall response rate (based on the Histiocyte Society criteria), disease reactivation rate, toxicity, permanent consequences, and survival rate corresponding to this treatment. The lung involvement outcome was based on serial lung function tests. The distribution of right-censored end points was estimated by the Kaplan-Meier method. Univariate Cox model with time-fixed and time-varying covariates was used for the predictive analysis of reactivation in the responders. Univariate analyses of risk factors for neurotoxicity were based on nonparametric Wilcoxon rank sum tests and exact Fisher tests.

resultsThe median duration of the first course of vinblastine was 7.6 months, with a median cumulative dose of 160 mg [IQR 120-212]. Seventy percent of the patients were responders at the end of this treatment. Subsequently, LCH reactivation occurred with a 5-year cumulative incidence of 40%. During the study, 27 reactivations were observed in 17 patients, and half of these episodes were retreated with vinblastine. At the end of the last vinblastine treatment, 70% of the patients were responders. None of the patients with impaired lung function improved. No grade 3-4 peripheral neuropathy was observed. At the final vinblastine treatment, permanent LCH consequences, primarily pituitary stalk involvement, were present in 15 (43%) patients, and all were present at the time of vinblastine initiation. The 10-year survival rate was 86.2% (95CI, 71.8-100%), and the 2 patients who died from LCH had risk organ localizations.

conclusionsVinblastine is an effective and well-tolerated first-line treatment for adult LCH except in patients with lung involvement and impaired lung function. However, a significant portion of patients experienced LCH reactivation during long-term follow up. As in childhood LCH, the presence of risk organ involvement has a negative impact on patient prognosis.

Indexed as

AdultAntineoplastic Agents, PhytogenicFemaleFollow-Up StudiesHistiocytosis, Langerhans-CellHumansMaleMiddle AgedRetrospective StudiesSurvival RateVinblastineAntineoplastic Agents, PhytogenicVinblastineLangerhans cell histiocytosisLungRecurrenceToxicityVinblastine

Identifiers

PMID28532436
PMCPMC5441059
OpenAlexW2618382588

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.