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Clinical and Laboratory Features of Patients with Marginal Zone Lymphoma: A Single Center Experience

Year 2023, Volume: 45 Issue: 2, 259 - 268, 15.03.2023
https://doi.org/10.20515/otd.1205914

Abstract

Marginal zone lymphoma (MZL) is a slowly progressing subtype of Non-Hodgkin Lymphoma (NHL). There are four subtypes: extranodal MZL of mucosa-associated lymphoid tissue (MALT lymphoma), nodal MZL, splenic MZL, and primary cutaneous MZL. Due to its heterogeneity and rarity, treatment management in MZL has not been clearly defined. In this study, clinical features and survival data of 36 patients with MZL were examined. The mean total follow-up period of the patients was 64.5 months. Follow-up periods ranged from 6 to 240 months. Thirty-two (88.8%) of the patients were alive. The median OS was 54 months. There were 4 patients (11.1%) who died and 22 (61%) patients who had relapsed. The median PFS was 45 months. Sixteen (44.5%) patients received CHOP or R-CHOP, 13 (36.1%) patients received weekly rituximab, 3 (8.3%) patients received rituximab-bendamustine. When treatment responses were evaluated, complete response was found in 22 (61.1%) patients, stable disease in 9 (25%) and partial response in 5 (13.9%). No progressive disease was observed in the response evaluation performed at the end of the first-line treatment. In our study, the effects of variables such as age, gender, stage, MALT-IPI score, treatment response, lactate dehydrogenase (LDH), β2-microglobulin, albumin, bone marrow infiltration at the time of diagnosis, liver involvement and non-hematopoietic area involvement on survival were examined. No significant effects were found (p>0.05). MALT-IPI score (p=0.029) and β2-microglobulin elevation (p=0.041) were found to be risk factors with adverse effects on PFS according to univariate survival analysis. According to the results of multivariate analysis, no statistically significant effects on survival were found (p>0.05). MALT-IPI score can be used to predict disease prognosis, but according to the results obtained from our study, adding β2-microglobulin to this score may be considered. Evaluating MZL subtypes separately will reduce the difficulty in interpreting results due to patient heterogeneity.

References

  • 1. Teras LR, DeSantis CE, Cerhan JR, et al. 2016 US lymphoid malignancy statistics by World Health Organization subtypes. CA Cancer J Clin 2016;66:443-59
  • 2. Alaggio R, Amador C, Anagnostopoulos I, Attygalle AD, Araujo IB de O, Berti E, vd. The 5th edition of the World Health Organization classification of haematolymphoid tumours: lymphoid neoplasms. Leukemia. 2022;36(7):1720-48.
  • 3. Swerdlow SH, Campo E, Harris NL, et al. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. Revised Fourth Edition. IARC, 2017.
  • 4. Zucca E, Bertoni F. The spectrum of MALT lymphoma at different sites: biological and therapeutic relevance. Blood. 2016;127:2082-2092.
  • 5. Khalil MO, Morton LM, Devesa SS, et al. Incidence of marginal zone lymphoma in the United States, 2001-2009 with a focus on primary anatomic site. Br J Haematol 2014;165:67-77.
  • 6. Price EJ, Rauz S, Tappuni AR, et al. The British Society for Rheumatology guideline for the management of adults with primary Sjögren’s syndrome. Rheumatology (Oxford) 2017;56:1643-7.
  • 7. Cerhan JR, Habermann TM. Epidemiology of marginal zone lymphoma. Ann Lymphoma. 2021;5:1.
  • 8. Zucca E, Arcaini L, Buske C, et al. Marginal zone lymphomas: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2020;31:17-29
  • 9. Sriskandarajah P, Dearden CE. Epidemiology and environmental aspects of marginal zone lymphomas. Best Pract Res Clin Haematol. 2017;30:84-91.
  • 10. Reid R, Friedberg JW. Management of marginal zone lymphoma. Oncology (Williston Park). 2013;27:840-842-844.
  • 11. Raderer M, Wöhrer S, Streubel B, et al. Assessment of disease dissemination in gastric compared with extragastric mucosa-associated lymphoid tissue lymphoma using extensive staging: a singlecenter experience. J Clin Oncol. 2006;24:3136-3141.
  • 12. Chae H, Cho H, Sa H-S, et al. The limited role of comprehensive staging work-up in ocular adnexal extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue type (MALToma) with excellent prognosis. Br J Haematol. 2021;193:848-851.
  • 13. Thieblemont C, Cascione L, Conconi A, et al. A MALT lymphoma prognostic index. Blood. 2017;130:1409-1417.
  • 14. Luminari S, Merli M, Rattotti S, et al. Early progression as a predictor of survival in marginal zone lymphomas: an analysis from the FIL-NF10 study. Blood 2019;134:798-801.
  • 15. Mulligan SP, Matutes E, Dearden C, Catovsky D. Splenic lymphoma with villous lymphocytes. Natural history and response to therapy in 50 cases. British Journal of Haematology. 1991;78:206–9.
  • 16. Troussard X, Valensi F, Duchayne E, et al. Splenic lymphoma with villous lymphocytes: clinical presentation, biology and prognostic factors in a series of 100 patients. Groupe Francais d’Hematologie Cellulaire (GFHC). Br J Haematol. 1996;93:731–6.
  • 17. Goda JS, Gospodarowicz M, Pintilie M, et al. Long-term outcome in localized extranodal mucosa-associated lymphoid tissue lymphomas treated with radiotherapy. Cancer, 2010; 116:3815-24.
  • 18. Zucca E, Conconi A, Pedrinis E, et al. International Extranodal Lymphoma Study Group Nongastric marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue. Blood, 2003;101:2489-95.
  • 19. Teckie S, Lovie S, Navarett S, Yahalom J. Clinical outcomes and patterns of relapse in 320 patients with early and advanced-stage marginal zone lymphoma: the role of radiotherapy. Hematol Oncol, 2013;31:130.
  • 20. Raderer M, Wöhrer S, Streubel B, et al. Assessment of disease dissemination in gastric compared with extragastric mucosa-associated lymphoid tissue lymphoma using extensive staging: a single-center experience. J Clin Oncol, 2006;24:3136-41.
  • 21. Zucca E, Stathis A, Bertoni F. The management of nongastric MALT lymphomas. Oncology (Williston Park), 2014;28:86-93.
  • 22. Dreyling M, Thieblemont C, Gallamini A, et al. ESMO Consensus conferences: guidelines on malignant lymphoma. part 2: marginal zone lymphoma, mantle cell lymphoma, peripheral T-cell lymphoma. Ann Oncol, 2013;24:857-77.
  • 23. Treglia G, Zucca E, Sadeghi R et al. Detection rate of fluorine-18-fluorodeoxyglucose positron emission tomography in patients with marginal zone lymphoma of MALT type: a meta-analysis. Hematol Oncol, 2015;33:113-24.
  • 24. Chacon J, Mollejo M, Munoz E, et al. Splenic marginal zone lymphoma: clinical characteristics and prognostic factors in a series of 60 patients. Blood. 2002;100:1648–54.
  • 25. Oh SY, Kim WS, Kim JS, et al. Phase II study of R-CVP followed by rituximab maintenance therapy for patients with advanced marginal zone lymphoma: Consortium for Improving Survival of Lymphoma (CISL) study. Cancer Commun (Lond). 2019;39:58.
  • 26. Salar A, Domingo-Domenech E, Panizo C, et al. First-line response-adapted treatment with the combination of bendamustine and rituximab in patients with mucosa-associated lymphoid tissue lymphoma (MALT2008-01): a multicentre, single-arm, phase 2 trial. Lancet Haematol. 2014;1:104-11.
  • 27. Alderuccio JP, Beaven AW, Shouse G, et al. Frontline bendamustine and rituximab in extranodal marginal zone lymphoma: an international analysis. Blood. 2020;136(Suppl 1):2-3.
  • 28. Knauf W, Abenhardt W, Koenigsmann M, et al. Rare lymphomas in routine practice - treatment and outcome in marginal zone lymphoma in the prospective German Tumour Registry Lymphatic Neoplasms. Hematol Oncol. 2021;39: 313-325.
  • 29. Thieblemont C, Felman P, Berger F, et al. Treatment of splenic marginal zone B-cell lymphoma: an analysis of 81 patients. Clin Lymphoma. 2002;3:41–47.
  • 30. Thieblemont C, Bastion Y, Berger F, et al. Mucosa-associated lymphoid tissue gastrointestinal and nongastrointestinal lymphoma behavior: analsyis of 108 patients. J Clin Oncol. 1997;15:1624-30.
  • 31. Radaszkiewicz T, Dragosics B, Bauer P. Gastrointestinal malignant lymphomas of the mucosa-associated lymphoid tissue: factors relevant to prognosis. Gastroenterology. 1992;102:1628-38.
  • 32. Montalban C. Abraira V. Arcaini L.et al. Risk stratification for splenic marginal zone lymphoma based on haemoglobin concentration, platelet count, high lactate dehydrogenase level and extrahilar lymphadenopathy: development and validation on 593 cases. Br J Haematol. 2012; 159: 164-171

Marjinal Zon Lenfomalı Hastaların Klinik ve Laboratuar Özellikleri: Tek Merkez Deneyimi

Year 2023, Volume: 45 Issue: 2, 259 - 268, 15.03.2023
https://doi.org/10.20515/otd.1205914

Abstract

Marjinal zon lenfoma (MZL), Non-Hodgkin Lenfoma (NHL)’nın yavaş seyirli bir alt tipidir. Mukoza ilişkili lenfoid dokunun ekstranodal MZL’sı (MALT lenfoma), nodal MZL, splenik MZL, primer kutanöz MZL olmak üzere dört alt tipi vardır. Heterojenitesi ve nadirliği sebebiyle MZL’da tedavi yönetimi net olarak tanımlanamamıştır. Bu çalışmada MZL tanılı 36 hastanın klinik özellikleri ve sağkalım verileri incelenmiştir. Hastaların toplam takip süresi ortalama 64.5 aydı. Takip süreleri 6-240 ay arasındaydı. Hastaların 32’si (%88.8) hayattaydı. Ortanca OS 54 aydı. Ölen 4 hasta (%11.1), relaps olan 22 (%61) hasta vardı. Ortanca PFS 45 aydı. On altı (%44.5) hasta CHOP veya R-CHOP, 13 (%36.1) hasta haftalık rituksimab, 3 (%8.3) hasta rituksimab-bendamustin tedavileri almıştı. Tedavi yanıtları değerlendirildiğinde 22 (%61.1) hastada tam yanıt, 9’unda (%25) stabil hastalık, 5’inde (%13.9) kısmi yanıt saptandı. İlk sıra tedavi bitiminde yapılan yanıt değerlendirilmesinde progresif hastalık görülmedi. Çalışmamızda yaş, cinsiyet, evre, MALT-IPI skoru, tedavi yanıtı, laktat dehidrogenaz (LDH), β2-mikroglobulin, albümin, tanı anında kemik iliği infiltrasyonu, karaciğer tutulumu ve hematopoetik olmayan alan tutulumu gibi değişkenlerin sağkalım üzerine etkileri incelendi ancak OS üzerine istatistiksel olarak anlamlı etkileri saptanmadı (p>0.05). MALT-IPI skoru (p=0.029) ve β2-mikroglobulin yüksekliğinin (p=0.041) tek değişkenli sağkalım analizine göre PFS üzerine olumsuz etkileri olan birer risk faktörü oldukları görüldü. Çoklu değişkenli analiz sonuçlarına göre ise sağkalım üzerine istatistiksel olarak anlamlı etkileri saptanmadı (p>0.05). MALT-IPI skoru hastalık prognozunu öngörmede kullanılabilir ancak çalışmamızdan elde edilen sonuçlara göre bu skora β2-mikroglobulin eklenmesi düşünülebilir. MZL alt tiplerinin ayrı ayrı değerlendirilmesi hasta heterojenitesine bağlı sonuçların yorumlanmasındaki güçlüğü azaltacaktır.

References

  • 1. Teras LR, DeSantis CE, Cerhan JR, et al. 2016 US lymphoid malignancy statistics by World Health Organization subtypes. CA Cancer J Clin 2016;66:443-59
  • 2. Alaggio R, Amador C, Anagnostopoulos I, Attygalle AD, Araujo IB de O, Berti E, vd. The 5th edition of the World Health Organization classification of haematolymphoid tumours: lymphoid neoplasms. Leukemia. 2022;36(7):1720-48.
  • 3. Swerdlow SH, Campo E, Harris NL, et al. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. Revised Fourth Edition. IARC, 2017.
  • 4. Zucca E, Bertoni F. The spectrum of MALT lymphoma at different sites: biological and therapeutic relevance. Blood. 2016;127:2082-2092.
  • 5. Khalil MO, Morton LM, Devesa SS, et al. Incidence of marginal zone lymphoma in the United States, 2001-2009 with a focus on primary anatomic site. Br J Haematol 2014;165:67-77.
  • 6. Price EJ, Rauz S, Tappuni AR, et al. The British Society for Rheumatology guideline for the management of adults with primary Sjögren’s syndrome. Rheumatology (Oxford) 2017;56:1643-7.
  • 7. Cerhan JR, Habermann TM. Epidemiology of marginal zone lymphoma. Ann Lymphoma. 2021;5:1.
  • 8. Zucca E, Arcaini L, Buske C, et al. Marginal zone lymphomas: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2020;31:17-29
  • 9. Sriskandarajah P, Dearden CE. Epidemiology and environmental aspects of marginal zone lymphomas. Best Pract Res Clin Haematol. 2017;30:84-91.
  • 10. Reid R, Friedberg JW. Management of marginal zone lymphoma. Oncology (Williston Park). 2013;27:840-842-844.
  • 11. Raderer M, Wöhrer S, Streubel B, et al. Assessment of disease dissemination in gastric compared with extragastric mucosa-associated lymphoid tissue lymphoma using extensive staging: a singlecenter experience. J Clin Oncol. 2006;24:3136-3141.
  • 12. Chae H, Cho H, Sa H-S, et al. The limited role of comprehensive staging work-up in ocular adnexal extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue type (MALToma) with excellent prognosis. Br J Haematol. 2021;193:848-851.
  • 13. Thieblemont C, Cascione L, Conconi A, et al. A MALT lymphoma prognostic index. Blood. 2017;130:1409-1417.
  • 14. Luminari S, Merli M, Rattotti S, et al. Early progression as a predictor of survival in marginal zone lymphomas: an analysis from the FIL-NF10 study. Blood 2019;134:798-801.
  • 15. Mulligan SP, Matutes E, Dearden C, Catovsky D. Splenic lymphoma with villous lymphocytes. Natural history and response to therapy in 50 cases. British Journal of Haematology. 1991;78:206–9.
  • 16. Troussard X, Valensi F, Duchayne E, et al. Splenic lymphoma with villous lymphocytes: clinical presentation, biology and prognostic factors in a series of 100 patients. Groupe Francais d’Hematologie Cellulaire (GFHC). Br J Haematol. 1996;93:731–6.
  • 17. Goda JS, Gospodarowicz M, Pintilie M, et al. Long-term outcome in localized extranodal mucosa-associated lymphoid tissue lymphomas treated with radiotherapy. Cancer, 2010; 116:3815-24.
  • 18. Zucca E, Conconi A, Pedrinis E, et al. International Extranodal Lymphoma Study Group Nongastric marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue. Blood, 2003;101:2489-95.
  • 19. Teckie S, Lovie S, Navarett S, Yahalom J. Clinical outcomes and patterns of relapse in 320 patients with early and advanced-stage marginal zone lymphoma: the role of radiotherapy. Hematol Oncol, 2013;31:130.
  • 20. Raderer M, Wöhrer S, Streubel B, et al. Assessment of disease dissemination in gastric compared with extragastric mucosa-associated lymphoid tissue lymphoma using extensive staging: a single-center experience. J Clin Oncol, 2006;24:3136-41.
  • 21. Zucca E, Stathis A, Bertoni F. The management of nongastric MALT lymphomas. Oncology (Williston Park), 2014;28:86-93.
  • 22. Dreyling M, Thieblemont C, Gallamini A, et al. ESMO Consensus conferences: guidelines on malignant lymphoma. part 2: marginal zone lymphoma, mantle cell lymphoma, peripheral T-cell lymphoma. Ann Oncol, 2013;24:857-77.
  • 23. Treglia G, Zucca E, Sadeghi R et al. Detection rate of fluorine-18-fluorodeoxyglucose positron emission tomography in patients with marginal zone lymphoma of MALT type: a meta-analysis. Hematol Oncol, 2015;33:113-24.
  • 24. Chacon J, Mollejo M, Munoz E, et al. Splenic marginal zone lymphoma: clinical characteristics and prognostic factors in a series of 60 patients. Blood. 2002;100:1648–54.
  • 25. Oh SY, Kim WS, Kim JS, et al. Phase II study of R-CVP followed by rituximab maintenance therapy for patients with advanced marginal zone lymphoma: Consortium for Improving Survival of Lymphoma (CISL) study. Cancer Commun (Lond). 2019;39:58.
  • 26. Salar A, Domingo-Domenech E, Panizo C, et al. First-line response-adapted treatment with the combination of bendamustine and rituximab in patients with mucosa-associated lymphoid tissue lymphoma (MALT2008-01): a multicentre, single-arm, phase 2 trial. Lancet Haematol. 2014;1:104-11.
  • 27. Alderuccio JP, Beaven AW, Shouse G, et al. Frontline bendamustine and rituximab in extranodal marginal zone lymphoma: an international analysis. Blood. 2020;136(Suppl 1):2-3.
  • 28. Knauf W, Abenhardt W, Koenigsmann M, et al. Rare lymphomas in routine practice - treatment and outcome in marginal zone lymphoma in the prospective German Tumour Registry Lymphatic Neoplasms. Hematol Oncol. 2021;39: 313-325.
  • 29. Thieblemont C, Felman P, Berger F, et al. Treatment of splenic marginal zone B-cell lymphoma: an analysis of 81 patients. Clin Lymphoma. 2002;3:41–47.
  • 30. Thieblemont C, Bastion Y, Berger F, et al. Mucosa-associated lymphoid tissue gastrointestinal and nongastrointestinal lymphoma behavior: analsyis of 108 patients. J Clin Oncol. 1997;15:1624-30.
  • 31. Radaszkiewicz T, Dragosics B, Bauer P. Gastrointestinal malignant lymphomas of the mucosa-associated lymphoid tissue: factors relevant to prognosis. Gastroenterology. 1992;102:1628-38.
  • 32. Montalban C. Abraira V. Arcaini L.et al. Risk stratification for splenic marginal zone lymphoma based on haemoglobin concentration, platelet count, high lactate dehydrogenase level and extrahilar lymphadenopathy: development and validation on 593 cases. Br J Haematol. 2012; 159: 164-171
There are 32 citations in total.

Details

Primary Language Turkish
Subjects Health Care Administration
Journal Section ORİJİNAL MAKALE
Authors

Fatih Yaman 0000-0002-0494-571X

Nur Oguz Davutoglu 0000-0003-3898-3527

Filiz Yavaşoğlu 0000-0002-4017-4668

Neslihan Andıc 0000-0003-0510-4733

Hava Üsküdar Teke 0000-0002-4434-4580

Eren Gunduz 0000-0001-7455-2949

Publication Date March 15, 2023
Published in Issue Year 2023 Volume: 45 Issue: 2

Cite

Vancouver Yaman F, Oguz Davutoglu N, Yavaşoğlu F, Andıc N, Üsküdar Teke H, Gunduz E. Marjinal Zon Lenfomalı Hastaların Klinik ve Laboratuar Özellikleri: Tek Merkez Deneyimi. Osmangazi Tıp Dergisi. 2023;45(2):259-68.


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