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Erschienen in: Annals of Hematology 5/2009

01.05.2009 | Original Article

Hodgkin lymphoma in Tyrol—a population-based study

verfasst von: Dominic Fong, Michael Steurer, Richard Greil, Eberhard Gunsilius, Gilbert Spizzo, Guenther Gastl, Alexandar Tzankov

Erschienen in: Annals of Hematology | Ausgabe 5/2009

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Abstract

We aimed to analyze the epidemiology, clinical characteristics, and outcome of patients with Hodgkin lymphoma (HL) diagnosed in Tyrol. All patients with newly diagnosed HL between 1993 and 2005 were included in this study. Among the 158 cases included, nodular lymphocytic predominant HL (nodular paragranuloma) was identified in ten cases (6%) whereas the majority of patients had classical Hodgkin lymphoma. Age (p < 0.01), sex (p = 0.03), risk groups according to the German Hodgkin Study Group stratification (p < 0.01), and bone marrow infiltration (p < 0.01) were of prognostic significance considering overall survival (OS) whereas histological subtype and bulky disease were not. The 5- and 10-year OS rates for the total group were 89% and 85%, respectively. Notably, in patients with advanced-stage HL (n = 49), combined modality treatment resulted in significantly better OS than chemotherapy alone (p = 0.01). Three patients developed a second hematological malignancy and one patient developed breast cancer. However, five patients (3%) had a malignant hematological disorder before occurrence of HL. Concerning treatment-related toxicity, bleomycin-associated lung toxicity was observed in six (4%) patients and five (3%) developed lethal treatment-related infectious complications. Our results provide evidence that the incidence rate of HL in Tyrol is comparable to other Western countries. Modern risk-adapted treatment results in excellent long-term prognosis but may be complicated by serious nonhematological side effects, in particular, infections and bleomycin-induced lung toxicity. Furthermore, 3% of HL patients had an antecedent malignant hematological disease before occurrence of HL.
Literatur
1.
Zurück zum Zitat Parkin DM, Muir CS (1992) Cancer incidence in five continents. Comparability and quality of data. IARC Sci Publ 45–173 Parkin DM, Muir CS (1992) Cancer incidence in five continents. Comparability and quality of data. IARC Sci Publ 45–173
5.
Zurück zum Zitat Jaffe ES, Lee Harris N, Stein H, Vardiman JW (2001) World Health Organization Classification of tumors. Pathology and genetics of tumors of haematopoietic and lymphoid tissues. IARC Press, Lyon Jaffe ES, Lee Harris N, Stein H, Vardiman JW (2001) World Health Organization Classification of tumors. Pathology and genetics of tumors of haematopoietic and lymphoid tissues. IARC Press, Lyon
7.
Zurück zum Zitat Gutensohn N, Cole P (1981) Childhood social environment and Hodgkin’s disease. N Engl J Med 304:135–140PubMed Gutensohn N, Cole P (1981) Childhood social environment and Hodgkin’s disease. N Engl J Med 304:135–140PubMed
9.
Zurück zum Zitat Jarrett RF, MacKenzie J (1999) Epstein-Barr virus and other candidate viruses in the pathogenesis of Hodgkin’s disease. Semin Hematol 36:260–269PubMed Jarrett RF, MacKenzie J (1999) Epstein-Barr virus and other candidate viruses in the pathogenesis of Hodgkin’s disease. Semin Hematol 36:260–269PubMed
10.
Zurück zum Zitat Alexander FE, Ricketts TJ, McKinney PA, Cartwright RA (1991) Community lifestyle characteristics and incidence of Hodgkin’s disease in young people. Int J Cancer 48:10–14PubMedCrossRef Alexander FE, Ricketts TJ, McKinney PA, Cartwright RA (1991) Community lifestyle characteristics and incidence of Hodgkin’s disease in young people. Int J Cancer 48:10–14PubMedCrossRef
11.
12.
Zurück zum Zitat Jarrett RF, Stark GL, White J, Angus B, Alexander FE, Krajewski AS et al (2005) Impact of tumor Epstein-Barr virus status on presenting features and outcome in age-defined subgroups of patients with classic Hodgkin lymphoma: a population-based study. Blood 106:2444–2451. doi:10.1182/blood-2004-09-3759 PubMedCrossRef Jarrett RF, Stark GL, White J, Angus B, Alexander FE, Krajewski AS et al (2005) Impact of tumor Epstein-Barr virus status on presenting features and outcome in age-defined subgroups of patients with classic Hodgkin lymphoma: a population-based study. Blood 106:2444–2451. doi:10.​1182/​blood-2004-09-3759 PubMedCrossRef
14.
Zurück zum Zitat Weiss LM, Strickler JG, Warnke RA, Purtilo DT, Sklar J (1987) Epstein-Barr viral DNA in tissues of Hodgkin’s disease. Am J Pathol 129:86–91PubMed Weiss LM, Strickler JG, Warnke RA, Purtilo DT, Sklar J (1987) Epstein-Barr viral DNA in tissues of Hodgkin’s disease. Am J Pathol 129:86–91PubMed
17.
Zurück zum Zitat Rosenberg SA (1996) The management of Hodgkin’s disease: half a century of change. The Kaplan Memorial Lecture. Ann Oncol 7:555–560PubMed Rosenberg SA (1996) The management of Hodgkin’s disease: half a century of change. The Kaplan Memorial Lecture. Ann Oncol 7:555–560PubMed
18.
Zurück zum Zitat Bonadonna G, Bonfante V, Viviani S, Di Russo A, Villani F, Valagussa P (2004) ABVD plus subtotal nodal versus involved-field radiotherapy in early-stage Hodgkin’s disease: long-term results. J Clin Oncol 22:2835–2841. doi:10.1200/JCO.2004.12.170 PubMedCrossRef Bonadonna G, Bonfante V, Viviani S, Di Russo A, Villani F, Valagussa P (2004) ABVD plus subtotal nodal versus involved-field radiotherapy in early-stage Hodgkin’s disease: long-term results. J Clin Oncol 22:2835–2841. doi:10.​1200/​JCO.​2004.​12.​170 PubMedCrossRef
19.
Zurück zum Zitat Engert A, Schiller P, Josting A, Herrmann R, Koch P, Sieber M et al (2003) Involved-field radiotherapy is equally effective and less toxic compared with extended-field radiotherapy after four cycles of chemotherapy in patients with early-stage unfavorable Hodgkin’s lymphoma: results of the HD8 trial of the German Hodgkin’s Lymphoma Study Group. J Clin Oncol 21:3601–3608. doi:10.1200/JCO.2003.03.023 PubMedCrossRef Engert A, Schiller P, Josting A, Herrmann R, Koch P, Sieber M et al (2003) Involved-field radiotherapy is equally effective and less toxic compared with extended-field radiotherapy after four cycles of chemotherapy in patients with early-stage unfavorable Hodgkin’s lymphoma: results of the HD8 trial of the German Hodgkin’s Lymphoma Study Group. J Clin Oncol 21:3601–3608. doi:10.​1200/​JCO.​2003.​03.​023 PubMedCrossRef
20.
Zurück zum Zitat Meyer RM, Gospodarowicz MK, Connors JM, Pearcey RG, Bezjak A, Wells WA et al (2005) Randomized comparison of ABVD chemotherapy with a strategy that includes radiation therapy in patients with limited-stage Hodgkin’s lymphoma: National Cancer Institute of Canada Clinical Trials Group and the Eastern Cooperative Oncology Group. J Clin Oncol 23:4634–4642. doi:10.1200/JCO.2005.09.085 PubMedCrossRef Meyer RM, Gospodarowicz MK, Connors JM, Pearcey RG, Bezjak A, Wells WA et al (2005) Randomized comparison of ABVD chemotherapy with a strategy that includes radiation therapy in patients with limited-stage Hodgkin’s lymphoma: National Cancer Institute of Canada Clinical Trials Group and the Eastern Cooperative Oncology Group. J Clin Oncol 23:4634–4642. doi:10.​1200/​JCO.​2005.​09.​085 PubMedCrossRef
21.
Zurück zum Zitat Canellos GP, Anderson JR, Propert KJ, Nissen N, Cooper MR, Henderson ES et al (1992) Chemotherapy of advanced Hodgkin’s disease with MOPP, ABVD, or MOPP alternating with ABVD. N Engl J Med 327:1478–1484PubMed Canellos GP, Anderson JR, Propert KJ, Nissen N, Cooper MR, Henderson ES et al (1992) Chemotherapy of advanced Hodgkin’s disease with MOPP, ABVD, or MOPP alternating with ABVD. N Engl J Med 327:1478–1484PubMed
22.
Zurück zum Zitat Gobbi PG, Levis A, Chisesi T, Broglia C, Vitolo U, Stelitano C et al (2005) ABVD versus modified Stanford V versus MOPPEBVCAD with optional and limited radiotherapy in intermediate- and advanced-stage Hodgkin’s lymphoma: final results of a multicenter randomized trial by the Intergruppo Italiano Linfomi. J Clin Oncol 23:9198–9207. doi:10.1200/JCO.2005.02.907 PubMedCrossRef Gobbi PG, Levis A, Chisesi T, Broglia C, Vitolo U, Stelitano C et al (2005) ABVD versus modified Stanford V versus MOPPEBVCAD with optional and limited radiotherapy in intermediate- and advanced-stage Hodgkin’s lymphoma: final results of a multicenter randomized trial by the Intergruppo Italiano Linfomi. J Clin Oncol 23:9198–9207. doi:10.​1200/​JCO.​2005.​02.​907 PubMedCrossRef
23.
Zurück zum Zitat Diehl V, Franklin J, Pfreundschuh M, Lathan B, Paulus U, Hasenclever D et al (2003) Standard and increased-dose BEACOPP chemotherapy compared with COPP-ABVD for advanced Hodgkin’s disease. N Engl J Med 348:2386–2395. doi:10.1056/NEJMoa022473 PubMedCrossRef Diehl V, Franklin J, Pfreundschuh M, Lathan B, Paulus U, Hasenclever D et al (2003) Standard and increased-dose BEACOPP chemotherapy compared with COPP-ABVD for advanced Hodgkin’s disease. N Engl J Med 348:2386–2395. doi:10.​1056/​NEJMoa022473 PubMedCrossRef
25.
Zurück zum Zitat Aleman BM, van den Belt-Dusebout AW, Klokman WJ, Van’t Veer MB, Bartelink H, van Leeuwen FE (2003) Long-term cause-specific mortality of patients treated for Hodgkin’s disease. J Clin Oncol 21:3431–3439. doi:10.1200/JCO.2003.07.131 PubMedCrossRef Aleman BM, van den Belt-Dusebout AW, Klokman WJ, Van’t Veer MB, Bartelink H, van Leeuwen FE (2003) Long-term cause-specific mortality of patients treated for Hodgkin’s disease. J Clin Oncol 21:3431–3439. doi:10.​1200/​JCO.​2003.​07.​131 PubMedCrossRef
26.
Zurück zum Zitat Diehl V, Fuchs M (2007) Early, intermediate and advanced Hodgkin’s lymphoma: modern treatment strategies. Ann Oncol 18(Suppl 9):71–79. doi:10.1093/annonc/mdm297 Diehl V, Fuchs M (2007) Early, intermediate and advanced Hodgkin’s lymphoma: modern treatment strategies. Ann Oncol 18(Suppl 9):71–79. doi:10.​1093/​annonc/​mdm297
28.
Zurück zum Zitat Segi M, Fujisaku S, Kurihara M, Narai Y, Sasajima K (1960) The age-adjusted death rates for malignant neoplasms in some selected sites in 23 countries in 1954–1955 and their geographical correlation. Tohoku J Exp Med 72:91–103PubMedCrossRef Segi M, Fujisaku S, Kurihara M, Narai Y, Sasajima K (1960) The age-adjusted death rates for malignant neoplasms in some selected sites in 23 countries in 1954–1955 and their geographical correlation. Tohoku J Exp Med 72:91–103PubMedCrossRef
29.
Zurück zum Zitat Ries LA, Kosary CL, Hankey BF, Miller BA, Clegg LX, Edwards BK (2000) SEER cancer statistics review, 1973–1996. NIH Pub. No.99-2789. National Cancer Institute, Bethesda Ries LA, Kosary CL, Hankey BF, Miller BA, Clegg LX, Edwards BK (2000) SEER cancer statistics review, 1973–1996. NIH Pub. No.99-2789. National Cancer Institute, Bethesda
32.
Zurück zum Zitat Josting A, Wiedenmann S, Franklin J, May M, Sieber M, Wolf J et al (2003) Secondary myeloid leukemia and myelodysplastic syndromes in patients treated for Hodgkin’s disease: a report from the German Hodgkin’s Lymphoma Study Group. J Clin Oncol 21:3440–3446. doi:10.1200/JCO.2003.07.160 PubMedCrossRef Josting A, Wiedenmann S, Franklin J, May M, Sieber M, Wolf J et al (2003) Secondary myeloid leukemia and myelodysplastic syndromes in patients treated for Hodgkin’s disease: a report from the German Hodgkin’s Lymphoma Study Group. J Clin Oncol 21:3440–3446. doi:10.​1200/​JCO.​2003.​07.​160 PubMedCrossRef
33.
Zurück zum Zitat Behringer K, Josting A, Schiller P, Eich HT, Bredenfeld H, Diehl V et al (2004) Solid tumors in patients treated for Hodgkin’s disease: a report from the German Hodgkin Lymphoma Study Group. Ann Oncol 15:1079–1085. doi:10.1093/annonc/mdh273 PubMedCrossRef Behringer K, Josting A, Schiller P, Eich HT, Bredenfeld H, Diehl V et al (2004) Solid tumors in patients treated for Hodgkin’s disease: a report from the German Hodgkin Lymphoma Study Group. Ann Oncol 15:1079–1085. doi:10.​1093/​annonc/​mdh273 PubMedCrossRef
35.
36.
Zurück zum Zitat Ng AK, Bernardo MV, Weller E, Backstrand K, Silver B, Marcus KC et al (2002) Second malignancy after Hodgkin disease treated with radiation therapy with or without chemotherapy: long-term risks and risk factors. Blood 100:1989–1996. doi:10.1182/blood-2002-02-0634 PubMedCrossRef Ng AK, Bernardo MV, Weller E, Backstrand K, Silver B, Marcus KC et al (2002) Second malignancy after Hodgkin disease treated with radiation therapy with or without chemotherapy: long-term risks and risk factors. Blood 100:1989–1996. doi:10.​1182/​blood-2002-02-0634 PubMedCrossRef
37.
Zurück zum Zitat van Leeuwen FE, Klokman WJ, Hagenbeek A, Noyon R, van den Belt-Dusebout AW, van Kerkhoff EH et al (1994) Second cancer risk following Hodgkin’s disease: a 20-year follow-up study. J Clin Oncol 12:312–325PubMed van Leeuwen FE, Klokman WJ, Hagenbeek A, Noyon R, van den Belt-Dusebout AW, van Kerkhoff EH et al (1994) Second cancer risk following Hodgkin’s disease: a 20-year follow-up study. J Clin Oncol 12:312–325PubMed
39.
Zurück zum Zitat Engel C, Loeffler M, Schmitz S, Tesch H, Diehl V (2000) Acute hematologic toxicity and practicability of dose-intensified BEACOPP chemotherapy for advanced stage Hodgkin’s disease. German Hodgkin’s Lymphoma Study Group (GHSG). Ann Oncol 11:1105–1114. doi:10.1023/A:1008301225839 PubMedCrossRef Engel C, Loeffler M, Schmitz S, Tesch H, Diehl V (2000) Acute hematologic toxicity and practicability of dose-intensified BEACOPP chemotherapy for advanced stage Hodgkin’s disease. German Hodgkin’s Lymphoma Study Group (GHSG). Ann Oncol 11:1105–1114. doi:10.​1023/​A:​1008301225839 PubMedCrossRef
40.
Zurück zum Zitat Dorr RT (1992) Bleomycin pharmacology: mechanism of action and resistance, and clinical pharmacokinetics. Semin Oncol 19:3–8PubMed Dorr RT (1992) Bleomycin pharmacology: mechanism of action and resistance, and clinical pharmacokinetics. Semin Oncol 19:3–8PubMed
42.
Zurück zum Zitat Holoye PY, Luna MA, MacKay B, Bedrossian CW (1978) Bleomycin hypersensitivity pneumonitis. Ann Intern Med 88:47–49PubMed Holoye PY, Luna MA, MacKay B, Bedrossian CW (1978) Bleomycin hypersensitivity pneumonitis. Ann Intern Med 88:47–49PubMed
43.
Zurück zum Zitat Van Barneveld PW, van der Mark TW, Sleijfer DT, Mulder NH, Koops HS, Sluiter HJ et al (1984) Predictive factors for bleomycin-induced pneumonitis. Am Rev Respir Dis 130:1078–1081PubMed Van Barneveld PW, van der Mark TW, Sleijfer DT, Mulder NH, Koops HS, Sluiter HJ et al (1984) Predictive factors for bleomycin-induced pneumonitis. Am Rev Respir Dis 130:1078–1081PubMed
44.
Zurück zum Zitat Dearnaley DP, Horwich A, A’Hern R, Nicholls J, Jay G, Hendry WF et al (1991) Combination chemotherapy with bleomycin, etoposide and cisplatin (BEP) for metastatic testicular teratoma: long-term follow-up. Eur J Cancer 27:684–691PubMedCrossRef Dearnaley DP, Horwich A, A’Hern R, Nicholls J, Jay G, Hendry WF et al (1991) Combination chemotherapy with bleomycin, etoposide and cisplatin (BEP) for metastatic testicular teratoma: long-term follow-up. Eur J Cancer 27:684–691PubMedCrossRef
45.
Zurück zum Zitat Jules-Elysee K, White DA (1990) Bleomycin-induced pulmonary toxicity. Clin Chest Med 11:1–20PubMed Jules-Elysee K, White DA (1990) Bleomycin-induced pulmonary toxicity. Clin Chest Med 11:1–20PubMed
46.
Zurück zum Zitat Levi JA, Raghavan D, Harvey V, Thompson D, Sandeman T, Gill G et al (1993) The importance of bleomycin in combination chemotherapy for good-prognosis germ cell carcinoma. Australasian Germ Cell Trial Group. J Clin Oncol 11:1300–1305PubMed Levi JA, Raghavan D, Harvey V, Thompson D, Sandeman T, Gill G et al (1993) The importance of bleomycin in combination chemotherapy for good-prognosis germ cell carcinoma. Australasian Germ Cell Trial Group. J Clin Oncol 11:1300–1305PubMed
47.
Zurück zum Zitat Real E, Roca MJ, Vinuales A, Pastor E, Grau E (1999) Life threatening lung toxicity induced by low doses of bleomycin in a patient with Hodgkin’s disease. Haematologica 84:667–668PubMed Real E, Roca MJ, Vinuales A, Pastor E, Grau E (1999) Life threatening lung toxicity induced by low doses of bleomycin in a patient with Hodgkin’s disease. Haematologica 84:667–668PubMed
48.
Zurück zum Zitat Bredenfeld H, Franklin J, Nogova L, Josting A, Fries S, Mailander V et al (2004) Severe pulmonary toxicity in patients with advanced-stage Hodgkin’s disease treated with a modified bleomycin, doxorubicin, cyclophosphamide, vincristine, procarbazine, prednisone, and gemcitabine (BEACOPP) regimen is probably related to the combination of gemcitabine and bleomycin: a report of the German Hodgkin’s Lymphoma Study Group. J Clin Oncol 22:2424–2429. doi:10.1200/JCO.2004.09.114 PubMedCrossRef Bredenfeld H, Franklin J, Nogova L, Josting A, Fries S, Mailander V et al (2004) Severe pulmonary toxicity in patients with advanced-stage Hodgkin’s disease treated with a modified bleomycin, doxorubicin, cyclophosphamide, vincristine, procarbazine, prednisone, and gemcitabine (BEACOPP) regimen is probably related to the combination of gemcitabine and bleomycin: a report of the German Hodgkin’s Lymphoma Study Group. J Clin Oncol 22:2424–2429. doi:10.​1200/​JCO.​2004.​09.​114 PubMedCrossRef
49.
Metadaten
Titel
Hodgkin lymphoma in Tyrol—a population-based study
verfasst von
Dominic Fong
Michael Steurer
Richard Greil
Eberhard Gunsilius
Gilbert Spizzo
Guenther Gastl
Alexandar Tzankov
Publikationsdatum
01.05.2009
Verlag
Springer-Verlag
Erschienen in
Annals of Hematology / Ausgabe 5/2009
Print ISSN: 0939-5555
Elektronische ISSN: 1432-0584
DOI
https://doi.org/10.1007/s00277-008-0618-1

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