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Single center experience in patients with a diagnosis of nodular lymphocyte predominant Hodgkin lymphoma

Year 2021, Volume: 3 Issue: Supplement 1, 40 - 41, 07.03.2021
https://doi.org/10.46310/tjim.877049

Abstract

Nodular lymphocyte predominant Hodgkin lymphoma is an infrequent disease. It is associated with a favorable prognosis. The most important problems with the management of the disease are relapses, transformation to non-Hodgkin lymphoma, and treatment-related toxicities. In early stages of disease, watchful waiting, surgery, radiotherapy, and single-agent rituximab are the treatment options. Chemo-immunotherapy may be preferred in early disease with high tumor and symptom burden. In advanced disease, chemo-immunotherapy with or without radiotherapy is used. Good responses can be achieved in relapsed disease. The risk of transformation is high. It is reasonable to obtain re-biopsies at relapses. Transformed disease and the primary disease have been shown to be clonally-related in most cases. Prognosis of transformed disease which is treated with salvage chemo-immunotherapy followed by autologous stem cell transplantation is similar to that of de novo diffuse large B-cell lymphoma. All of the data regarding the treatment come from retrospective data.

References

  • Spinner MA, Varma G, Advani RH. Modern principles in the management of nodular lymphocyte-predominant Hodgkin lymphoma. Br J Haematol. 2019 Jan;184(1):17-29. doi: 10.1111/bjh.15616. Epub 2018 Nov 28. PMID: 30485408.
  • Hartmann S, Eichenauer DA. Nodular lymphocyte predominant Hodgkin lymphoma: pathology, clinical course and relation to T-cell/histiocyte rich large B-cell lymphoma. Pathology. 2020 Jan;52(1):142-153. doi: 10.1016/j.pathol.2019.10.003. Epub 2019 Nov 28. PMID: 31785822.
  • Borchmann S, Joffe E, Moskowitz CH, Zelenetz AD, Noy A, Portlock CS, Gerecitano JF, Batlevi CL, Caron PC, Drullinsky P, Hamilton A, Hamlin PA Jr, Horwitz SM, Kumar A, Matasar MJ, Moskowitz AJ, Owens CN, Palomba ML, Younes A, Straus DJ. Active surveillance for nodular lymphocyte-predominant Hodgkin lymphoma. Blood. 2019 May 16;133(20):2121-2129. doi: 10.1182/blood-2018-10-877761. Epub 2019 Feb 15. PMID: 30770396; PMCID: PMC7022227.
Year 2021, Volume: 3 Issue: Supplement 1, 40 - 41, 07.03.2021
https://doi.org/10.46310/tjim.877049

Abstract

References

  • Spinner MA, Varma G, Advani RH. Modern principles in the management of nodular lymphocyte-predominant Hodgkin lymphoma. Br J Haematol. 2019 Jan;184(1):17-29. doi: 10.1111/bjh.15616. Epub 2018 Nov 28. PMID: 30485408.
  • Hartmann S, Eichenauer DA. Nodular lymphocyte predominant Hodgkin lymphoma: pathology, clinical course and relation to T-cell/histiocyte rich large B-cell lymphoma. Pathology. 2020 Jan;52(1):142-153. doi: 10.1016/j.pathol.2019.10.003. Epub 2019 Nov 28. PMID: 31785822.
  • Borchmann S, Joffe E, Moskowitz CH, Zelenetz AD, Noy A, Portlock CS, Gerecitano JF, Batlevi CL, Caron PC, Drullinsky P, Hamilton A, Hamlin PA Jr, Horwitz SM, Kumar A, Matasar MJ, Moskowitz AJ, Owens CN, Palomba ML, Younes A, Straus DJ. Active surveillance for nodular lymphocyte-predominant Hodgkin lymphoma. Blood. 2019 May 16;133(20):2121-2129. doi: 10.1182/blood-2018-10-877761. Epub 2019 Feb 15. PMID: 30770396; PMCID: PMC7022227.
There are 3 citations in total.

Details

Primary Language English
Subjects ​Internal Diseases
Journal Section Short Report
Authors

Ömer Candar 0000-0001-7602-6926

Fahir Özkalemkaş 0000-0001-9710-134X

Vildan Ozkocaman 0000-0003-0014-7398

Tuba Ersal This is me 0000-0001-5419-3221

İbrahim Ethem Pınar 0000-0001-9907-1498

Cumali Yalçın This is me 0000-0002-5129-2977

Bedrettin Orhan 0000-0003-3970-2344

Publication Date March 7, 2021
Submission Date February 18, 2021
Acceptance Date March 5, 2021
Published in Issue Year 2021 Volume: 3 Issue: Supplement 1

Cite

EndNote Candar Ö, Özkalemkaş F, Ozkocaman V, Ersal T, Pınar İE, Yalçın C, Orhan B (March 1, 2021) Single center experience in patients with a diagnosis of nodular lymphocyte predominant Hodgkin lymphoma. Turkish Journal of Internal Medicine 3 Supplement 1 40–41.

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