ArticleOrphanet journal of rare diseases2017
Vinblastine chemotherapy in adult patients with langerhans cell histiocytosis: a multicenter retrospective study.
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.
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Who cites it
28 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.
- Pulmonary langerhans cell histiocytosis secondary to Marijuana use: a case report and systematic review of the literature.BMC pulmonary medicine · 2025Pooled it
- Phase 2 study using low dose cytarabine for adult patients with newly diagnosed Langerhans cell histiocytosis.Leukemia · 2024Trial
- Low Bone Mass in Probable CD1a-negative Langerhans Cell Histiocytosis: A Diagnostic Challenge.JCEM case reports · 2025Article
- Unusual Long-Term Survival in an Adult Patient With Langerhans Cell Histiocytosis and Central Nervous System Involvement: A Case Report.Case reports in hematology · 2025Article
- Langerhans cell histiocytosis misdiagnosed as thyroid malignancy: A case report.World journal of clinical cases · 2023Article
- Incidence, prevalence and survival in patients with Langerhans cell histiocytosis: A national registry study from England, 2013-2019.British journal of haematology · 2022Article
- Langerhans cell histiocytosis in adolescent patients: a single-centre retrospective study.Orphanet journal of rare diseases · 2022Article
- Role ofQuantitative imaging in medicine and surgery · 2022Article
- Article
- Adult Langerhans Cell Histiocytosis and the Skeleton.Journal of clinical medicine · 2022Review
- Three-dimensional printed titanium pseudo-prosthesis for the treatment of a tumoral bone defect.JSES reviews, reports, and techniques · 2022Article
- Histiocytic disorders.Nature reviews. Disease primers · 2021Review
- Three decades of progress from surgery to medical therapy for isolated neuroaxisJournal of neurosurgery. Case lessons · 2021Article
- Nasal oral fistula revealing Langerhans´ cell histiocytosis in adult patient: case report.The Pan African medical journal · 2021Article
- Neutralizing Anti-IL-17A Antibody Demonstrates Preclinical Activity Enhanced by Vinblastine in Langerhans Cell Histiocytosis.Frontiers in oncology · 2021Article
- Article
- Histiocytic disorders: insights into novel biology and implications for therapy of Langerhans cell histiocytosis and Erdheim-Chester disease.Hematology. American Society of Hematology. Education Program · 2020Article
- Clinical features and outcomes of adult Langerhans cell histiocytosis: a single-center experience.International journal of hematology · 2020Article
- Paediatric pulmonary Langerhans cell histiocytosis.Breathe (Sheffield, England) · 2020Review
- Update on Pulmonary Langerhans Cell Histiocytosis.Frontiers in medicine · 2020Review
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Authors and funding
15 authors at 10 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
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.
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