Z Orthop Unfall 2017; 155(05): 575-586
DOI: 10.1055/s-0043-110224
Übersicht
Georg Thieme Verlag KG Stuttgart · New York

Multiples Myelom – aktuelle Standards in Diagnostik und Therapie

Multiple Myeloma – Current Status in Diagnostic Testing and Therapy
Michael Kehrer
Klinik und Poliklinik für Orthopädie und Unfallchirurgie, Universitätsklinikum Bonn
,
Sebastian Koob
Klinik und Poliklinik für Orthopädie und Unfallchirurgie, Universitätsklinikum Bonn
,
Andreas Strauss
Klinik und Poliklinik für Orthopädie und Unfallchirurgie, Universitätsklinikum Bonn
,
Dieter Christian Wirtz
Klinik und Poliklinik für Orthopädie und Unfallchirurgie, Universitätsklinikum Bonn
,
Jan Schmolders
Klinik und Poliklinik für Orthopädie und Unfallchirurgie, Universitätsklinikum Bonn
› Author Affiliations
Further Information

Publication History

Publication Date:
14 August 2017 (online)

Zusammenfassung

Hintergrund Das multiple Myelom (MM) ist als maligne hämatologische Systemerkrankung nach Einteilung der Weltgesundheitsorganisation (WHO) dem Formenkreis der Plasmazellneoplasien zuzuordnen. Die weltweite Inzidenzrate des MM liegt etwa bei 6 – 7/100 000 Einwohnern/Jahr und macht somit etwa 1% aller Krebserkrankungen der Welt aus. In Deutschland sind ca. 6000 Neuerkrankungen pro Jahr zu verzeichnen. Im Zeitalter der sog. neuen Therapiesubstanzen wie Immunmodulatoren, Proteasomeninhibitoren und Antikörpern haben sich in der Behandlung des MM enorme Fortschritte ergeben. Auf dem Fachgebiet der Orthopädie und Unfallchirurgie ist es von großer Bedeutung, die Leitsymptome des MM im klinischen Alltag sicher zu erkennen und durch eine zielgerichtete Basisdiagnostik weiter abzuklären. Die operative Versorgung von myelomassoziierten Skelettläsionen, wie etwa die Stabilisierung von pathologischen Frakturen, ist Aufgabe der orthopädischen Chirurgie.

Methoden Auf Grundlage einer umfassenden Literaturrecherche, die selektiv in PubMed mit den Stichworten „multiple myeloma“ and „diagnostic“ or „therapy“ erfolgte, wurde die verfügbare Primär- und Sekundärliteratur zu aktuellen Standards in der Diagnostik und Therapie des MM beurteilt. Eingeschlossen wurden systematische Reviews, Metaanalysen, klinischen Studien und internationale Therapieempfehlungen bis Frühjahr 2016.

Ergebnisse Es existieren heute sehr sensitive Nachweismethoden in der Diagnostik des MM, die neben der bildgebenden Skelettdiagnostik und histologischen Knochenmarkuntersuchung insbesondere die klinisch-chemische Serum- und Urindiagnostik, einschließlich eines 24-h-Sammelurins umfassen. Nach heutigem Kenntnisstand besteht das therapeutische Grundkonzept aus der Kombination einer Hochdosischemotherapie (HDT) und einer autologen Blutstammzelltransplantation (ASCT). Die einzelnen Therapiesäulen der meist multimodalen Behandlungsstrategie sind in enger fachübergreifender Zusammenarbeit patientengerecht abzuwägen. Hierbei ist für die Bewertung des Risikoprofils des Patienten das Lebensalter, die Komorbiditäten sowie der individuelle Krankheitsverlauf (Rezidivneigung oder therapierefraktäre Krankheitsprogression) zu berücksichtigen. Bei Patienten > 70. – 75. Lebensjahr und/oder schweren Komorbiditäten, für die eine HDT und ASCT i. d. R. ungeeignet ist, müssen Indikationen für konventionelle Therapieoptionen gestellt werden. Darüber hinaus sind supportive Behandlungsmaßnahmen wie die Gabe von Bisphosphonaten zur Knochenprotektion, stabilisierende Operationen von pathologischen Frakturen oder eine lokale Strahlenbehandlung von schmerzhaften Osteolysen in das gesamtheitliche Therapiekonzept des MM einzubinden.

Schlussfolgerung In aktuellen Studienuntersuchungen konnte gezeigt werden, dass neue Wirkstoffgruppen wie Proteasomenhemmer, immunmodulatorische Substanzen und Antikörper bereits vielversprechend in der Behandlung des MM eingesetzt werden können, um die Prognose und Lebensqualität von Myelompatienten in Zukunft weiter zu verbessern. Hierbei werden die Therapiealgorithmen komplexer und kostenintensiver.

Abstract

Background Multiple myeloma is a haematological blood cancer of the bone marrow and is classified by the World Health Organisation (WHO) as a plasma cell neoplasm. In multiple myeloma, normal plasma cells transform into malignant myeloma cells and produce large quantities of an abnormal immunoglobulin called monoclonal protein or M protein. This ultimately causes multiple myeloma symptoms such as bone damage or kidney problems. The annual worldwide incidence of multiple myeloma is estimated to be 6 – 7/100,000 and accounts for 1% of all cancer. In Germany, there are about 6,000 cases of newly diagnosed multiple myeloma per annum. In the current era of new agents, such as immunomodulatory drugs and proteasome inhibitors and antibodies, enormous progress has been achieved in the therapy of multiple myeloma. In orthopaedics, it is essential to be able to recognise the of alarming symptoms of multiple myeloma in clinical routine and to be aware of basic diagnostic features to confirm this disease. Surgical treatment of myeloma-related bone lesions – such as stabilisation of pathological fractures – is an important domain of tumour orthopaedic surgery.

Methods A comprehensive literature search was performed in PubMed using the keywords “multiple myeloma” and “diagnostic” or “therapy”. This served to evaluate the available primary and secondary literature on the current status of the diagnostic testing and therapy of multiple myeloma. Systematic reviews, meta-analyses and clinical studies as well as international recommendations in therapy were included until the spring of 2016.

Results There are now very sensitive screening methods for the diagnosis of multiple myeloma. Accurate diagnosis is generally based on several factors, including physical evaluation, patient history, symptoms, and diagnostic testing results. The standards for initial diagnostic tests are determined by blood and urine tests as well as a bone marrow biopsy and skeletal imaging, such as X-rays, CT scans and MRI scans. Major and minor criteria are required to confirm the diagnosis of multiple myeloma and help to determine the classification and staging of multiple myeloma, and whether it is smoldering myeloma (asymptomatic), symptomatic myeloma, or a monoclonal gammopathy of undetermined significance (MGUS). Multiple myeloma treatment options have increased significantly over the last 10 years. Standard of basic myeloma treatment consists of high dose chemotherapy in combination with autologous stem cell transplantation. Several factors may determine multiple myeloma treatment, such as age and general health, results of laboratory and cytogenetic (genomic) tests as well as symptoms and disease complications. After evaluation of these factors, an individual and often multimodal treatment plan is created and implemented in interdisciplinary cooperation. Conventional treatment options have to be evaluated for older patients (> 70 – 75 years), who are not eligible for high dose chemotherapy and autologous stem cell transplantation due to their age and/or severe comorbidities. It is essential to include supportive therapy in the integral treatment concept, in order to control pain or retain function or mobility. Supportive drugs such as bisphosphonates but also radiation therapy and orthopaedic surgery may be required in order to manage complications of the disease as well as side effects of treatment.

Conclusion Current studies show promising results in the treatment of multiple myeloma, due to new agents such as immunomodulatory drugs, proteasome inhibitors and antibodies, which may improve prognosis and survival rate among myeloma patients in the future. However treatment algorithms have become more complex and expensive.

 
  • Literatur

  • 1 Sabattini E, Bacci F, Sagramoso C. et al. WHO classification of tumours of haematopoietic and lymphoid tissues in 2008: an overview. Pathologica 2010; 102: 83-87
  • 2 Harousseau JL, Moreau P. Autologous hematopoietic stem-cell transplantation for multiple myeloma. N Engl J Med 2009; 360: 2645-2654
  • 3 Deutsches Krebsregister. Krebs in Deutschland 2011/2012. Multiples Myelom 2015. Im Internet: www.krebsdaten.de https://www.krebsdaten.de/Krebs/DE/Content/Publikationen/Krebs_in_Deutschland/kid_2015/kid_2015_c90_multiples_myelom.pdf?__blob=publicationFile Stand: Januar 2017
  • 4 Pulte D, Jansen L, Castro FA. et al. Trends in survival of multiple myeloma patients in Germany and the United States in the first decade of the 21st century. Br J Haematol 2015; 171: 189-196
  • 5 Ries LAG, Hankey BF, Miller BA. et al. Cancer Statistics Review 1973 – 1988. Washington, DC: U.S. Government Printing Office; 1991
  • 6 Devesa SS. Descriptive Epidemiology of multiple Myeloma. In: Obrams GI, Potter M. eds. Epidemiology and Biology of multiple Myeloma. Berlin: Springer; 1991: 3-12
  • 7 Gentile M, Recchia AG, Mazzone C. et al. Emerging biological insights and novel treatment strategies in multiple myeloma. Expert Opin Emerg Drugs 2012; 17: 407-438
  • 8 Rajkumar SV, Dimopoulos MA, Palumbo A. et al. International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma. Lancet Oncol 2014; 15: e538-e548
  • 9 International Myeloma Working Group. Criteria for the classification of monoclonal gammopathies, multiple myeloma and related disorders: a report of the International Myeloma Working Group. Br J Haematol 2003; 121: 749-757
  • 10 Landgren O, Kyle RA, Pfeiffer RM. et al. Monoclonal gammopathy of undetermined significance (MGUS) consistently precedes multiple myeloma: a prospective study. Blood 2009; 113: 5412-5417
  • 11 Kyle RA, Therneau TM, Rajkumar SV. et al. Prevalence of monoclonal gammopathy of undetermined significance. N Engl J Med 2006; 354: 1362-1369
  • 12 Palumbo A, Bringhen S, Mateos MV. et al. Geriatric assessment predicts survival and toxicities in elderly myeloma patients: an International Myeloma Working Group report. Blood 2015; 125: 2068-2074
  • 13 Kyle RA, Gertz MA, Witzig TE. et al. Review of 1027 patients with newly diagnosed multiple myeloma. Mayo Clin Proc 2003; 78: 21-33
  • 14 Kariyawasan CC, Hughes DA, Jayatillake MM. et al. Multiple myeloma: causes and consequences of delay in diagnosis. QJM 2007; 100: 635-640
  • 15 San Miguel JF, Gutierrez NC, Mateo G. et al. Conventional diagnostics in multiple myeloma. Eur J Cancer 2006; 42: 1510-1519
  • 16 Kjeldsen E. Identification of prognostically relevant chromosomal abnormalities in routine diagnostics of multiple myeloma using genomic profiling. Cancer Genomics Proteomics 2016; 13: 91-127
  • 17 Sawyer JR. The prognostic significance of cytogenetics and molecular profiling in multiple myeloma. Cancer Genet 2011; 204: 3-12
  • 18 Dimopoulos M, Kyle R, Fermand JP. et al. Consensus recommendations for standard investigative workup: report of the International Myeloma Workshop Consensus Panel 3. Blood 2011; 117: 4701-4705
  • 19 Stewart AK, Fonseca R. Review of molecular diagnostics in multiple myeloma. Expert Rev Mol Diagn 2007; 7: 453-459
  • 20 Sonneveld P, Avet-Loiseau H, Lonial S. et al. Treatment of multiple myeloma with high-risk cytogenetics: a consensus of the International Myeloma Working Group. Blood 2016; 127: 2955-2962
  • 21 Fonseca R, San Miguel J. Prognostic factors and staging in multiple myeloma. Hematol Oncol Clin North Am 2007; 21: 1115-1140
  • 22 Dimopoulos M, Terpos E, Comenzo RL. et al. International Myeloma Working Group consensus statement and guidelines regarding the current role of imaging techniques in the diagnosis and monitoring of multiple myeloma. Leukemia 2009; 23: 1545-1556
  • 23 Schreiman JS, McLeod RA, Kyle RA. et al. Multiple myeloma: evaluation by CT. Radiology 1985; 154: 483-486
  • 24 Cretti F, Perugini G. Patient dose evaluation for the whole-body low-dose multidetector CT (WBLDMDCT) skeleton study in multiple myeloma (MM). Radiol Med 2016; 121: 93-105
  • 25 Durie BG, Salmon SE. A clinical staging system for multiple myeloma. Correlation of measured myeloma cell mass with presenting clinical features, response to treatment, and survival. Cancer 1975; 36: 842-854
  • 26 Greipp PR, San Miguel J, Durie BG. et al. International staging system for multiple myeloma. J Clin Oncol 2005; 23: 3412-3420
  • 27 Conte LG, Figueroa MG, Lois VV. et al. [Prognostic value of the new international staging system in multiple myeloma. Comparison with Durie-Salmon staging system]. Rev Med Chil 2008; 136: 7-12
  • 28 Li J, Wu XB, Zhou Y. et al. [Screening of prognostic factors and comparing of staging systems of multiple myeloma]. Zhongguo Shi Yan Xue Ye Xue Za Zhi 2012; 20: 926-929
  • 29 Hari PN, Zhang MJ, Roy V. et al. Is the International Staging System superior to the Durie-Salmon staging system? A comparison in multiple myeloma patients undergoing autologous transplant. Leukemia 2009; 23: 1528-1534
  • 30 Alexanian R, Balcerzak S, Bonnet JD. et al. Prognostic factors in multiple myeloma. Cancer 1975; 36: 1192-1201
  • 31 Spasov E, Goranova V. Prognostic assessment of the Durie and Salmon staging system in patients with multiple myeloma. Folia Med (Plovdiv) 1998; 40: 121-123
  • 32 Anagnostopoulos A, Gika D, Symeonidis A. et al. Multiple myeloma in elderly patients: prognostic factors and outcome. Eur J Haematol 2005; 75: 370-375
  • 33 Haferlach T, Löffler H. Prognostic factors in multiple myeloma: practicability for clinical practice and future perspectives. Leukemia 1997; 11 (Suppl. 05) S5-S9
  • 34 Avet-Loiseau H, Hulin C, Campion L. et al. Chromosomal abnormalities are major prognostic factors in elderly patients with multiple myeloma: the intergroupe francophone du myélome experience. J Clin Oncol 2013; 31: 2806-2809
  • 35 Abdelgawad IA, Radwan NH, Shafik RE. et al. Significance of some proliferation markers and some prognostic factors in patients with multiple myeloma and their impact on the patientsʼ survival. Asian Pac J Cancer Prev 2016; 17: 2389-2394
  • 36 Takamatsu H, Honda S, Miyamoto T. et al. Changing trends in prognostic factors for patients with multiple myeloma after autologous stem cell transplantation during the immunomodulator drug/proteasome inhibitor era. Cancer Sci 2015; 106: 179-185
  • 37 Mateos MV, Hernandez MT, Giraldo P. et al. Lenalidomide plus dexamethasone for high-risk smoldering multiple myeloma. N Engl J Med 2013; 369: 438-447
  • 38 Attal M, Harousseau JL, Stoppa AM. et al. A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma. Intergroupe Français du Myélome. N Engl J Med 1996; 335: 91-97
  • 39 Le Ray E, Jagannath S, Palumbo A. Advances in targeted therapy for the treatment of patients with relapsed/refractory multiple myeloma. Expert Rev Hematol 2016; 9: 91-105
  • 40 Anderson KC. Targeted therapy for multiple myeloma. Semin Hematol 2001; 38: 286-294
  • 41 Izumi T. [Novel targeted therapy in multiple myeloma]. Nihon Rinsho 2014; 72: 1089-1093
  • 42 Kumar SK, Rajkumar SV, Dispenzieri A. et al. Improved survival in multiple myeloma and the impact of novel therapies. Blood 2008; 111: 2516-2520
  • 43 Shank BR, Brown VT, Schwartz RN. Multiple myeloma maintenance therapy: a review of the pharmacologic treatment. J Oncol Pharm Pract 2015; 21: 36-51
  • 44 Carrier M, Le Gal G, Tay J. et al. Rates of venous thromboembolism in multiple myeloma patients undergoing immunomodulatory therapy with thalidomide or lenalidomide: a systematic review and meta-analysis. J Thromb Haemost 2011; 9: 653-663
  • 45 Badros A, Goloubeva O, Dalal JS. et al. Neurotoxicity of bortezomib therapy in multiple myeloma: a single-center experience and review of the literature. Cancer 2007; 110: 1042-1049
  • 46 Palumbo A, Davies F, Kropff M. et al. Consensus guidelines for the optimal management of adverse events in newly diagnosed, transplant-ineligible patients receiving melphalan and prednisone in combination with thalidomide (MPT) for the treatment of multiple myeloma. Ann Hematol 2010; 89: 803-811
  • 47 Roy A, Kish JK, Bloudek L. et al. Estimating the costs of therapy in patients with relapsed and/or refractory multiple myeloma: a model framework. Am Health Drug Benefits 2015; 8: 204-215
  • 48 Muchtar E, Dingli D, Kumar S. et al. Autologous stem cell transplant for multiple myeloma patients 70 years or older. Bone Marrow Transplant 2016; 51: 1449-1455
  • 49 Merz M, Jansen L, Castro FA. et al. Survival of elderly patients with multiple myeloma-Effect of upfront autologous stem cell transplantation. Eur J Cancer 2016; 62: 1-8
  • 50 Badros A, Barlogie B, Siegel E. et al. Autologous stem cell transplantation in elderly multiple myeloma patients over the age of 70 years. Br J Haematol 2001; 114: 600-607
  • 51 Katragadda L, McCullough LM, Dai Y. et al. Effect of melphalan 140 mg/m(2) vs. 200 mg/m(2) on toxicities and outcomes in multiple myeloma patients undergoing single autologous stem cell transplantation – a single center experience. Clin Transplant 2016; 30: 894-900
  • 52 Gay F, Oliva S, Petrucci MT. et al. Chemotherapy plus lenalidomide versus autologous transplantation, followed by lenalidomide plus prednisone versus lenalidomide maintenance, in patients with multiple myeloma: a randomised, multicentre, phase 3 trial. Lancet Oncol 2015; 16: 1617-1629
  • 53 Palumbo A, Cavallo F, Gay F. et al. Autologous transplantation and maintenance therapy in multiple myeloma. N Engl J Med 2014; 371: 895-905
  • 54 Wang Y, Yang F, Shen Y. et al. Maintenance therapy with immunomodulatory drugs in multiple myeloma: a meta-analysis and systematic review. J Natl Cancer Inst 2015; 108: djv342
  • 55 Mohty M, Richardson PG, McCarthy PL. et al. Consolidation and maintenance therapy for multiple myeloma after autologous transplantation: where do we stand?. Bone Marrow Transplant 2015; 50: 1024-1029
  • 56 Joks M, Jurczyszyn A, Machaczka M. et al. The roles of consolidation and maintenance therapy with novel agents after autologous stem cell transplantation in patients with multiple myeloma. Eur J Haematol 2015; 94: 109-114
  • 57 Cook G, Williams C, Brown JM. et al. High-dose chemotherapy plus autologous stem-cell transplantation as consolidation therapy in patients with relapsed multiple myeloma after previous autologous stem-cell transplantation (NCRI Myeloma X Relapse [Intensive trial]): a randomised, open-label, phase 3 trial. Lancet Oncol 2014; 15: 874-885
  • 58 Singh Abbi KK, Zheng J, Devlin SM. et al. Second autologous stem cell transplant: an effective therapy for relapsed multiple myeloma. Biol Blood Marrow Transplant 2015; 21: 468-472
  • 59 Ludwig H, Sonneveld P. Disease control in patients with relapsed and/or refractory multiple myeloma: what is the optimal duration of therapy?. Leuk Res 2012; 36 (Suppl. 01) S27-S34
  • 60 Moreau P. The future of therapy for relapsed/refractory multiple myeloma: emerging agents and novel treatment strategies. Semin Hematol 2012; 49 (Suppl. 01) S33-S46
  • 61 Liu L, Zhao N, Xu W. et al. Pooled analysis of the reports of carfilzomib, panobinostat, and elotuzumab combinations in patients with refractory/relapsed multiple myeloma. J Hematol Oncol 2016; 9: 54
  • 62 Liu JD, Sun CY, Tang L. et al. Efficacy and safety of panobinostat in relapsed or/and refractory multiple myeloma: meta analyses of clinical trials and systematic review. Sci Rep 2016; 6: 27361
  • 63 Lonial S, Dimopoulos M, Palumbo A. et al. Elotuzumab therapy for relapsed or refractory multiple myeloma. N Engl J Med 2015; 373: 621-631
  • 64 Terpos E, Kleber M, Engelhardt M. et al. European Myeloma Network guidelines for the management of multiple myeloma-related complications. Haematologica 2015; 100: 1254-1266
  • 65 Ludwig H, Miguel JS, Dimopoulos MA. et al. International Myeloma Working Group recommendations for global myeloma care. Leukemia 2014; 28: 981-992
  • 66 Mhaskar R, Redzepovic J, Wheatley K. et al. Bisphosphonates in multiple myeloma: a network meta-analysis. Cochrane Database Syst Rev 2012; (05) CD003188
  • 67 Terpos E, Morgan G, Dimopoulos MA. et al. International Myeloma Working Group recommendations for the treatment of multiple myeloma-related bone disease. J Clin Oncol 2013; 31: 2347-2357