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Vinblastine chemotherapy in adult patients with langerhans cell histiocytosis: a multicenter retrospective study.
Tazi, Abdellatif; Lorillon, Gwenaël; Haroche, Julien; Neel, Antoine; Dominique, Stéphane; Aouba, Achille; Bouaziz, Jean-David; de Margerie-Melon, Constance; Bugnet, Emmanuelle; Cottin, Vincent; Comont, Thibault; Lavigne, Christian; Kahn, Jean-Emmanuel; Donadieu, Jean; Chevret, Sylvie.
Afiliação
  • Tazi A; Assistance 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.
  • Lorillon G; Université Paris Diderot, Sorbonne Paris Cité, Inserm UMR-1153 (CRESS), Biostatistics and Clinical Epidemiology research team (ECSTRA), Paris, France. abdellatif.tazi@aphp.fr.
  • Haroche J; Assistance 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.
  • Neel A; Assistance Publique-Hôpitaux de Paris, Hôpital Pitié Salpêtrière, Service de Médecine Interne, Université Pierre et Marie Curie, Paris, France.
  • Dominique S; CHU de Nantes, Hôpital Hôtel Dieu, Service de Médecine Interne, Nantes, France.
  • Aouba A; Département de Pneumologie, Hôpital Charles Nicolle, Rouen, France.
  • Bouaziz JD; Assistance Publique-Hôpitaux de Paris, Hôpital Cochin, Service de Médecine Interne, Paris, France.
  • de Margerie-Melon C; Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis, Département de Dermatologie, Univ Paris Diderot, Sorbonne Paris Cité, Inserm U976, Paris, France.
  • Bugnet E; Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis, Service de Radiologie, Paris, France.
  • Cottin V; Assistance 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.
  • Comont T; Groupement Hospitalier Est, Service de Pneumologie, Université Claude Bernard Lyon 1, Lyon, France.
  • Lavigne C; Institut Universitaire du Cancer de Toulouse-Oncopôle, CHU de Toulouse, Service de Médecine Interne, Toulouse, France.
  • Kahn JE; CHU Angers, Service de Médecine Interne et vasculaire, Angers, France.
  • Donadieu J; Université Saint-Quentin en Yvelines, Hôpital Foch, Service de Médecine Interne, Suresnes, France.
  • Chevret S; Assistance Publique-Hôpitaux de Paris, Hôpital Trousseau, Centre National de Référence de l'Histiocytose Langerhansienne, Service d'Hémato-Oncologie pédiatrique, Paris, France.
Orphanet J Rare Dis ; 12(1): 95, 2017 05 22.
Article em En | MEDLINE | ID: mdl-28532436
ABSTRACT

BACKGROUND:

Vinblastine 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.

RESULTS:

The 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.

CONCLUSIONS:

Vinblastine 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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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles / 7_ODS3_muertes_prevenibles_nacidos_ninos Base de dados: MEDLINE Assunto principal: Vimblastina / Histiocitose de Células de Langerhans / Antineoplásicos Fitogênicos Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles / 7_ODS3_muertes_prevenibles_nacidos_ninos Base de dados: MEDLINE Assunto principal: Vimblastina / Histiocitose de Células de Langerhans / Antineoplásicos Fitogênicos Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2017 Tipo de documento: Article