TumorDiagnostik & Therapie 2023; 44(01): 59-65
DOI: 10.1055/a-1958-4531
Thieme Onkologie aktuell

Management der Langerhans-Zell-Histiozytose bei erwachsenen Patienten

Management of adult patients with Langerhans cell histiocytosis
1   Klinik für Innere Medizin, St. Franziskus-Hospital, Köln, Deutschland
› Author Affiliations

Zusammenfassung

Die Langerhans-Zell-Histiozytose ist eine seltene myeloische Neoplasie aus dem Formenkreis der Histiozytosen. Durch entzündliche Gewebezerstörung mit Fibrosierung kann es in jedem Organ zu einer Dysfunktion kommen. Am häufigsten sind Skelett, Lungen und Haut betroffen. Symptome, insbesondere eine Hypophyseninsuffizienz, gehen der Diagnosestellung häufig Monate bis Jahre voraus. Der Krankheitsverlauf ist variabel und reicht von spontanen Rückbildungen bis hin zu chronisch rezidivierenden Verläufen. Die Therapiemaßnahmen richten sich nach Krankheitsaktivität, betroffenen Organen und Organdysfunktion. Aufgrund häufig zugrunde liegender somatischer Genmutationen im MAPK-Signaltransduktionsweg stehen jetzt auch gezielt wirksame Inhibitoren zur Verfügung. Die Prognose der Patienten ist günstig. Erkrankung oder Therapiemaßnahmen können jedoch zu irreversiblen Spätfolgen führen. Eine vor allem symptomorientierte Nachsorge ist empfehlenswert.

Abstract

Langerhans cell histiocytosis is a rare myeloid neoplasia from the group of histiocytoses. Inflammatory tissue destruction with fibrosis can cause dysfunction in any organ. The skeleton, lungs, and skin are most commonly affected. Symptoms, especially of pituitary insufficiency, often precede diagnosis by months to years. The course of the disease is variable, ranging from spontaneous regressions to chronic recurrent courses. Therapeutic measures depend on disease activity, affected organs and organ dysfunction. Due to frequently underlying somatic gene mutations in the MAPK signal transduction pathway, targeted inhibitors are now available. The prognosis of patients is favorable. Nevertheless, disease or therapy can lead to irreversible late effects. A primarily symptom-oriented follow-up is recommended.



Publication History

Article published online:
03 February 2023

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  • Literatur

  • 1 Emile JE, Abla O, Fraitag S. et al. Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages. Blood 2016; 127 (22) 2672-2681 DOI: 10.1182/blood-2016-01-690636. (PMID: 26966089)
  • 2 Baumgartner I, von Hochstetter A, Baumert B. et al. Langerhans’-cell histiocytosis in adults. Med Pediatr Oncol 1997; 28 (01) 9-14
  • 3 Vassallo R, Ryu JH, Schroeder DR. et al. Clinical outcomes of pulmonary Langerhans’-cell histiocytosis in adults. N Engl J Med 2002; 346 (07) 484-490 DOI: 10.1056/NEJMoa012087. (PMID: 11844849)
  • 4 Lee JS, Ko GH, Kim HC. et al. Langerhans cell sarcoma arising from Langerhans cell histiocytosis: a case report. J Korean Med Sci 2006; 21 (03) 577-580
  • 5 Goyal G, Hu M, Young JR. et al. Adult Langerhans cell histiocytosis: a contemporary single-institution series of 186 patients. J Clin Oncol 2019; 37 (Suppl. 15) 7018 DOI: 10.1200/JCO.2019.37.15_suppl.7018.
  • 6 Doberauer C, Bornemann C. Experiences of a single center in one hundred ninety-four adult patients with Langerhans cell histiocytosis. J Hematol 2022; 11 (04) 131-141 DOI: 10.14740/jh1020. (PMID: 36118552)
  • 7 Cao XX, Duan MH, Zhao AL. et al. Treatment outcomes and prognostic factors of patients with adult Langerhans cell histiocytosis. Am J Hematol 2022; 97 (02) 203-208
  • 8 Aricò M, Girschikofsky M, Généreau T. et al. Langerhans cell histiocytosis in adults. Report from the international registry of the Histocyte Society. Eur J Cancer 2003; 39 (16) 2341-2348
  • 9 Ferrell J, Sharp S, Kumar A. et al. Discrepancies between F-18-FDG PET/CT and conventional imaging in Langerhans cell histiocytosis. Pediatr Blood Cancer 2021; 68 (04) e28891 DOI: 10.1002/pbc.28891.
  • 10 Goyal G, Tazi A, Go RS. et al. International expert consensus recommendations for the diagnosis and treatment of Langerhans cell histiocytosis in adults. Blood 2022; 139 (17) 2601-2621 DOI: 10.1182/blood.2021014343. (PMID: 35271698)
  • 11 Tazi A, de Margerie C, Naccache JM. et al. The natural history of adult pulmonary Langerhans cell histiocytosis: a prospective multicentre study. Orphanet J Rare Dis 2015; 10: 30-39 DOI: 10.1186/s13023-015-0249-2. (PMID: 25887097)
  • 12 Yasko AW, Fanning CV, Ayala AG. et al. Percutaneous techniques for the diagnosis and treatment of localized Langerhans-cell histiocytosis (eosinophilic granuloma of bone). J Bone Joint Surg Am 1998; 80 (02) 219-228 DOI: 10.2106/00004623-199802000-00009. (PMID: 9486728)
  • 13 Kriz J, Eich HT, Bruns F. et al. Radiotherapy in Langerhans cell histiocytosis – a rare indication in a rare disease. Radiat Oncol 2013; 8: 233-238 DOI: 10.1186/1748-717X-8-233. (PMID: 24103738)
  • 14 Olschewski T, Seegenschmiedt MH. Radiotherapy of Langerhans’ cell histiocytosis: results and implications of a national patterns-of-care study. Strahlenther Onkol 2006; 182 (11) 629-634 DOI: 10.1007/s00066-006-1630-9. (PMID: 17072519)
  • 15 Saven A, Burian C. Cladribine activity in adult Langerhans-cell histiocytosis. Blood 1999; 93 (12) 4125-4130 (PMID: 10361109)
  • 16 Adam Z, Szturz P, Duras J. et al. Treatment of Langerhans cell histiocytosis by cladribine reached long-term complete remission in 9 out of 10 patients. Klin Onkol 2012; 25 (04) 255-261
  • 17 Cantu MA, Lupo PJ, Bilgi M. et al. Optimal therapy for adults with Langerhans cell histiocytosis bone lesions. PLOS 2012; 7 (08) e43257-e43261
  • 18 Morimoto A, Shimazaki C, Takahashi S. et al. Therapeutic outcome of multifocal Langerhans cell histiocytosis in adults treated with the special C regimen formulated by the Japan LCH Study Group. Int J Hematol 2012; 97 (01) 103-108
  • 19 Derenzi E, Stefoni V, Pellegrini C. et al. High efficacy of the MACOP-B regimen in the treatment of adult Langerhans cell histiocytosis, a 20 year experience. BMC Cancer 2015; 15: 879-884
  • 20 Duan MH, Han X, Li J. et al. Comparison of vindesine and prednisone and cyclophosphamide, etoposide, vindesine, and prednisone as first-line treatment for adult Langerhans cell histiocytosis: a single-center retrospective study. Leuk Res 2016; 42: 43-46 DOI: 10.1016/j.leukres.2016.01.012. (PMID: 26859782)
  • 21 Zinn DJ, Grimes AB, Lin H. et al. Hydroxyurea: a new old therapy for Langerhans cell histiocytosis. Blood 2016; 128 (20) 2462-2465 DOI: 10.1182/blood-2016-06-721993. (PMID: 27688802)
  • 22 Tazi A, Lorillon G, Haroche J. et al. Vinblastin chemotherapy in adult patients with Langerhans cell histiocytosis: a multicenter retrospective study. Orphanet J Rare Dis 2017; 12 (01) 95-104
  • 23 Goyal G, Abeykoon JP, Hu M. et al. Single-agent cladribine as an effective front-line therapy for adults with Langerhans cell histiocytosis. Am J Hematol 2021; 96 (05) E146-E150
  • 24 Cao XX, Li J, Zhao AL. et al. Methotrexate and cytarabine for adult patients with newly diagnosed Langerhans cell histiocytosis: A single arm, single center, prospective phase 2 study. Am J Hematol 2020; 95 (09) E235-E238
  • 25 Neel A, Artifoni M, Fontenoy AM. et al. Long-term efficacy and safety of 2CdA (cladribine) in extrapulmonary adult-onset Langerhans cell histiocytosis: analysis of 23 cases from the French Histiocytosis Group and systematic literature review. Br J Hematol 2020; 189 (05) 869-878
  • 26 Héritier S, Emile JF, Barkaoui MA. et al. BRAF mutation correlates with high-risk Langerhans cell histiocytosis and increased resistance to first-line therapy. J Clin Oncol 2016; 34 (25) 3023-3030
  • 27 Han X, Ouyang M, Duan M. et al. The combination of methotrexate and cytosine arabinoside in newly diagnosed adult Langerhans cell histiocytosis: a prospective phase II interventional clinical trial. BMC Cancer 2020; 20 (01) 433-444 DOI: 10.1186/s12885-020-06872-8. (PMID: 32423455)
  • 28 Pan Y, Xi R, Wang C. et al. Autologous hematopoetic stem cell transplantation for efficient treatment of multisystem, high-risk, BRAF V600E-negative Langerhans cell histiocytosis. J Int Med Res 2019; 47 (09) 4522-4529
  • 29 Gabalec F, Simkovic M, Zavrelova A. et al. Treatment of multifocal multisystem BRAF positive Langerhans cell histiocytosis with cladribine, surgery and allogenic stem cell transplantation. Acta Med (Hradec Kralove) 2017; 60 (04) 152-156
  • 30 Veys PA, Nanduri V, Baker KS. et al. Hematopoetic stem cell transplantation for refractory Langerhans cell histiocytosis: outcome by intensity of conditioning. Br J Haematol 2015; 169 (05) 711-718
  • 31 Diamond EL, Subbiah V, Lockhart AC. et al. Vemurafenib for BRAF V600-mutant Erdheim-Chester disease and Langerhans cell histiocytosis: analysis of data from the histology-independent, phase 2, open-label VE-BASKET study. JAMA 2018; 4 (03) 384-388
  • 32 Hazim AZ, Ruan GJ, Ravindran A. et al. Efficacy of BRAF-inhibitor therapy in BRAFV600E-mutated adult Langerhans cell histiocytosis. Oncologist 2020; 25 (12) 1001-1004
  • 33 Diamond EL, Durham BH, Ulaner GH. et al. Efficacy of MEK inhibition in patients with histocytic neoplasms. Nature 2019; 567: 521-524
  • 34 Eckstein O, Visser J, Rodriguez-Galindo C. et al. Clinical responses and persistent BRAF V600E+ blood cells in children with LCH treated with MAPK pathway inhibition. Blood 2019; 133 (15) 1691-1694
  • 35 Chellapandian D, Makras P, Kaltsas G. et al. Bisphosphonates in Langerhans cell histiozcytosis: an international retrospective case series. Mediterr J Hematol. Infect Dis 2016; 8 (01) e2016033 DOI: 10.4084/MJHID.2016.033.
  • 36 Wajda N, Zhu Z, Jandarov R. et al. Clinical outcomes and survival following lung transplantation in patients with pulmonary Langerhans cell histiocytosis. Respirology 2020; 25 (06) 644-650
  • 37 Griffiths W, Davies S, Gibbs P. et al. Liver transplantation in an adult with sclerosing cholangitis due to Langerhans cell histiocytosis. J Hepatol 2006; 44 (04) 829-831
  • 38 Haupt R, Minkov M, Astigarraga I. et al. Langerhans cell histiocytosis (LCH): guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years. Pediatr Blood Cancer 2013; 60 (02) 175-184 DOI: 10.1002/pbc.24367. (PMID: 23109216)
  • 39 Eckstein O, McAtee CL, Greenberg J. et al. Rituximab therapy for patients with Langerhans cell histiocytosis-associated neurologic dysfunction. Pediatr Hematol Oncol 2018; 35 (07) 427-433
  • 40 Euskirchen P, Haroche J, Emile JF. et al. Complete remission of critical neurohistiocytosis by vemurafenib. Neurol Neuroimmunol Neuroinflamm 2015; 2 (02) e78 DOI: 10.1212/NXI.0000000000000078. (PMID: 25745636)
  • 41 Swerdlow SH, Campo E, Pileri SA. et al. The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood 2016; 127 (20) 2375-2390 DOI: 10.1182/blood-2016-01-643569. (PMID: 26980727)
  • 42 Wu Y, Chen WY, Yang TX. et al. Langerhans cell sarcoma arising from antecedent langerhans cell histiocytosis: A case report. Medicine 2019; 98 (10) e14531 DOI: 10.1097/MD.0000000000014531.
  • 43 Gounder MM, Solit DB, Tap WD. Trametinib in histiocytic sarcoma with an activating MAP2K1 (MEK1) mutation. N Engl J Med 2018; 378 (20) 1945-1947 DOI: 10.1056/NEJMc1511490. (PMID: 29768143)