Yıl: 2021 Cilt: 54 Sayı: 1 Sayfa Aralığı: 115 - 127 Metin Dili: Türkçe DOI: 10.5505/aot.2021.82473 İndeks Tarihi: 15-06-2021

Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti

Öz:
Giriş ve amaç: Bu çalışmada 1990 yılında yapılmış Hodgkin lenfoma tezinden yola çıkılarakgünümüzde HL tanı, görüntüleme ve tedavi sindeki güncel gelişim vaka örneklemleri ile incelenecektir.Son 30 yıldaki tedavi endikasyonu değişimleri, radyoterapi tedavi alanlarındaki küçülmeler veradyoterapi doz düşümleri tarihsel süreçler dikkate alınarak karşılaşmalı olarak değerlendirilecektir.Yöntem ve gereçler: Yazarın 1985- 1990 yıları arasında Ankara Numune Hastanesi RadyoterapiKliniğinde tedavisi tamamlanan hastaların demografik ve klinik, özellikleri özetlenecek ve o tarihtekigüncel görüntüleme yöntemleri ve tedavi yaklaşımları, günümüzdeki yaklaşımlarla kıyaslanacaktır.Bulgular: 1985-1990 yılları arasında Ankara Numune Hastanesinde Hodgkin lenfoma tanısı ile tedaviedilen 60 vakanın verileri incelenmiştir. Ortanca yaş 31 olarak bulundu. Evre ve histolojik tip gruplararasında eşit olarak dağılmıştı. Başlangıç tutulum alanlar; servikal-supraklavikular bölge 34 vaka (%56), inguinofemoral 8 vaka (%13), aksiller 7 vaka (%11), mediastinal 5 vaka (%8,2), abdominal 3 vaka (% 5,3), tonsil 2 vaka (%3), primer beyin 1 vaka olarak görüldü. Diafram altı başlayan vakalar totalin% 18 lik bölümüydü. Miks sellüler tip en çok görülen gurubu oluşturdu. Bin dokuz yüz seksenli yıllardaEvre IA ve II A Hodgkin lenfoma da standart tedavi şekli Sub Total Lenfod Işınlama (Mantle, InvertedY) idi. Bu dönemde Hodgkin lenfoma görüntülemesinde kullanılan en gelişmiş yöntem Bi-PedalLenfanjigrafi iken günümüzde FDG PET-CT primer görüntüleme yöntemidir. Bu çalışmada radyoterapialan 58 hastanın 6 sında yineleme olmuştur. Yinelemelerin 4 ü alan dışı, 2 si alan içi olarak raporlanmıştıTartışma ve sonuç: Alan dışı nükslerin fazlalığı ve geniş alan radyoterapi uygulamalarının özellikleçocukluk yaş grubunda oluşturduğu büyüme gelişme gerilikleri, kardiak sorunlar, ikincil kanserlerinartışı gibi yan etkiler araştırmacıları yeni tedavi şekilleri aramaya yöneltmiştir. Günümüzde giderekboyut olarak küçülmüş ve dozu azaltılmış radyoteapi uygulamaları iyi kemoterapi uygulamaları ileeşleştirilmiştir. Hem kemoterapideki iyileşmeler hem de radyoterapi tekniğindeki gelişmeler 5 yıllıkyaşamı %90 seviyelerinin üzerine çıkarırken morbid yan etkiler tarihsel makalelerde anekdot olarakkalmıştır.
Anahtar Kelime:

Hodgkin Lymphoma Treatment; What Has Changed in the Last 30 Years

Öz:
Introduction: In this study, based on the Hodgkin lymphoma thesis made in 1990, current developments in Hodgkin lymphoma diagnosis, imaging and treatment are examined with case samples. Changes in treatment indication in the last 30 years, shrinkage in radiotherapy treatment areas and radiotherapy dose reductions are evaluated comparatively, taking into account historical processes. Methods: The demographic and clinical characteristics of the patients whose treatment was completed in the radiotherapy clinic of Ankara Numune Hospital between 1985-1990 will be summarized and the current imaging methods and treatment approaches at that time are compared with current approaches. Results: The data of 60 cases treated with the diagnosis of Hodgkin lymphoma in Ankara Numune Hospital between 1985-1990 are analyzed. The median age was 31. Histologic types and stages are distributed evenly between the groups. The initial involvement areas are such that; 34 cases start in the cervical-supraclavicular region (56%), eight in inguinofemoral (13%), seven in axillary (11%), five in mediastinal (8.2), three in the abdominal (5.3%), two in the tonsillar (3%), one in primary cerebral. Diseases that initiated under the diaphragm were 18% of the total. Mixcellular type constituted the most common group. In the 1980s, the standard treatment method for Stage IA and II A Hodgkin lymphoma was Sub Total Lymphoid Irradiation (Mantle, Inverted Y). In this period, the most advanced technique used in Hodgkin lymphoma imaging was Bi-Pedal Lymphangygraphy, while FDG PET-CT is the primary imaging method today. In this study, the number of recurrent patients is to be found 6 out of 58 who received radiotherapy. Four of them were outside the field, and two were within. Discussion and conclusion: The excessive number of out of field recurrences, side effects such as growth and development retardation, cardiac problems, and increase in secondary cancers caused (especially in the childhood age group) by wide-field radiotherapy applications; led researchers to seek new treatment modalities. Nowadays, applications of radiotherapy with reduced size and decreased dose combined with better chemotherapy practices. While improvements in both chemotherapy and radiotherapy techniques have increased the 5-year life above 90%, morbid side effects have remained anecdotal in historical articles
Anahtar Kelime:

Belge Türü: Makale Makale Türü: Araştırma Makalesi Erişim Türü: Erişime Açık
  • 1. Richard T. Hoppe. Hodgkin Lymphoma. In: Perez and Brady’s Principles and Practice of Radiation Oncology. (Lww.com). Lippincott Williams & Wilkins, a Wolters Kluwer. Philadelphia, 2013; 1531-47.
  • 2. Monika L. Metzger, Hiroto Inaba, Stephanie Terezakis, and Louis S. Constine. Lymphomas in children. In: Perez and Brady’s Principles and Practice of Radiation Oncology. Lww.com). Lippincott Williams & Wilkins, a Wolters Kluwer. Philadelphia, 2019; 1695- 1712.
  • 3. Kenneth B. Roberts, Kara M. Kelly, and Louis S. Constine. Pediatric Hodgkin’s Lymphoma. In: Guderson and Tepper, Clinical Radiation Oncology. (expert consult. inkling.com/ redeem). Elsevier, Philadelphia, 2016 ;1464-85.
  • 4. Andrea K. Ng, Lawrence M. Weiss, and Ann S. LaCasce. Hodgkin’s Lymphoma. In: Guderson and Tepper, Clinical Radiation Oncology. (expert consult.inkling.com/redeem). Elsevier, Philadelphia, 2016;1506-23.
  • 5. Mauz-Korholz C, Hasenclever D, Dorffel W, et al: Procarbazine-free OEPA-COPDAC chemotherapy in boys and standard OPPA-COPP in girls have comparable effectiveness in pediatric Hodgkin’s lymphoma: The GPOH-HD-2002 study. J Clin Oncol. 2010; 28(23):3680–3686.
  • 6. Group E-PHsL. Recommendations for the Diagnostics and Treatment of children and adolescents with a classical Hodgkin’s Lymphoma during the Interim phase between the end of the EuroNet-PHL-C1 Study and the start of the EuroNet-PHL-C2 Study. 2013; [cited 2014 January 4, 2014].
  • 7. Engert A, Schiller P, Josting A, et al. Involvedfield radiotherapy is equally effective and less toxic compared with extended-field radiotherapy after four cycles of chemotherapy in patients with early-stage unfavourable Hodgkin’s lymphoma: results of the HD8 trial of the German Hodgkin’s Lymphoma Study Group. J Clin Oncol 2003; 21: 3601–8.
  • 8. Metzger ML, Weinstein HJ, Hudson MM, et al: Association between radio-therapy vs no radiotherapy based on early response to VAMP chemotherapy and survival among children with favorable-risk Hodgkin lymphoma. JAMA. 2012; 307 (24): 2609–2616.
  • 9. Meyer RM, Gospodarowicz MK, Connors JM et al. ABVD alone versus radiation-based therapy in limited-stage Hodgkin’s lymphoma. N Engl J Med. 2012; 366(5): 399–408.
  • 10. Illidge T, Specht L, Yahalom J. Modern Radiation Therapy for Nodal Non-Hodgkin Lymphoma—Target Definition and Dose Guidelines From the International Lymphoma Radiation Oncology Group. IJROBP. 2014; 89 (1):49–58.
  • 11. Girinsky T, van der Maazen R, Specht L et al. Involved-node radiotherapy (INRT) in patients with early Hodgkin lymphoma: concepts and guidelines. Radiother Oncol. 2006; 79: 270–277.
  • 12. Bradford S. Hoppe and Richard T. Hoppe. In Target Volume Delineation for Conformal and Intensity-Modulated Radiation Therapy. (www. springer. com). Switzerland, 2015; 451-64.
  • 13. Yahalom J, Mauch P. The involved field is back: issues in delineating the radiation field in Hodgkin’s disease. Ann Oncol. 2002; 13(Suppl 1):79– 83.
  • 14. Dörffel W, Rühl U, Lüders H, et al: Treatment of children and adolescents with Hodgkin lymphoma without radiotherapy for patients in complete remission after chemotherapy: Final results of the multinational trial GPOH-HD95. J Clin Oncol. 2013; 31(12): 1562–1568.
  • 15. Kung FH, Schwartz CL, Ferree CR, et al. POG 8625: A randomized trial comparing chemotherapy with chemoradiotherapy for children and adolescents with Stages I, IIA, IIIA1 Hodgkin Disease: A report from the Children’s Oncology Group. J Pediatr Hematol Oncol. 2006; 28(6):362–368.
  • 16. Rigacci L, Vitolo U, Nassi L, et al.: Positron emission tomography in the staging of patients with Hodgkin’s lymphoma. A prospective multicentric study by the Intergruppo Italiano Linfomi. Ann Hematol. 2007; 86:897-903.
  • 17. Erturk SM, Van den Abbeele AD: Role of PET/CT scanning in initial and post-treatment assessment of Hodgkin disease. J Natl Compr Canc Netw. 2008; 6: 623-632.
  • 18. Hutchings M, Loft A, Hansen M, et al.: Position emission tomography with or without computed tomography in the primary staging of Hodgkin’s lymphoma. Haematologica. 2006; 91: 482-489.
  • 19. Pelosi E, Pregno P, Penna D, et al.: Role of whole-body [18F] fluorodeoxyglucose positron emission tomography/computed tomography (FDGPET/CT) and conventional techniques in the staging of patients with Hodgkin and aggressive non Hodgkin lymphoma. Radiol Med. 2008; 113: 578-590.
  • 20. Hoppe BS, Flampouri S, Su Z et al. (Consolidative involved- node proton therapy for Stage IA-IIIB mediastinal Hodgkin lymphoma: preliminary dosimetric outcomes from a Phase II study. Int J Radiat Oncol Biol Phys. 2012; 83(1): 260– 267.
  • 21. Tukenova M, Guibout C et al. Role of cancer treatment in long term overall and cardiovascular mortality after childhood cancer. J Clin Oncol. 2010; 28:1308–15.
  • 22. Travis LB, Gospodarowicz M et al. Lung cancer following chemotherapy and radiotherapy for Hodgkin’s disease. J Natl Cancer Inst. 2002; 94:182–92.
  • 23. Travis LB, Hill DA et al. Breast cancer following radiotherapy and chemotherapy among young women with Hodgkin disease. JAMA. 2003; 290:465–75.
  • 24. Specht L, Yahalom J, Illidge T et al. Modern radiation therapy for Hodgkin lymphoma: field and dose guidelines from the International Lymphoma Radiation Oncology Group (ILROG). Int J Radiat Oncol Biol Phys. 2014; 89(4): 854-62.
  • 25. Thar TL, Million RR, Hausner RJ, et al: Hodgkin’s disease, stages I and II: Relationship of recurrence to size of disease, radiation dose, and number of sites involved. Cancer. 1979; 43(3):1101– 1105.
  • 26. Keller FG, Castellino SM, Chen l, et al. Results of the AHOD0431 trial of response adopted therapy and salvage strategy for limited stage classical lymphoma: Report From Children Oncology Group. Cancer 2018; 124: 3210-3219.
  • 27. Mauz-Köholz C, hasenclaver D, Dörffell W, et al. Procarbazine free OEPA-COPDAC chemotherapy in boys and standart OPPA-COP in girls have comparable effectiveness in pediatric Hodgkin lymphoma: the GHOH-hd-2002 study. J Clin Oncol 2010; 28(23),3680- 3686.
  • 28. Diehl V, Brillant C, Engert A, et al. HD10: Investigating reduction of combined modality treatment intensity in early stage Hodgkin’s lymphoma. Interim analysis of a randomized trial of the German Hodgkin Study Group (GHSG) [Abstract]. J Clin Oncol 2005; 23: 16S–5561.
  • 29. NCCN Clinical Practise Guidelines in Oncology (NCCN Guidelines), Pediatric Hodgkin Lymphoma. NCCN.org. Version 2.2021-October 21,2020
  • 30. Landman-Parker J, Pacquement H, Leblanc T, et al: Localized childhood Hodgkin’s disease: Response-adapted chemotherapy with etoposide, bleomycin, vinblastine, and prednisone before lowdose radiation therapy results of the French Society of Pediatric Oncology Study MDH90. J Clin Oncol. 2000; 18(7):1500–1507.
  • 31. Donaldson SS, Hudson MM, Lamborn KR, et al: VAMP and low-dose, involved-field radiation for children and adolescents with favorable, early-stage Hodgkin’s disease: Results of a prospective clinical trial. J Clin Oncol. 2002; 20(14): 3081–3087.
  • 32. NCCN Clinical Practise Guidelines in Oncology (NCCN Guidelines), Hodgkin Lymphoma. NCCN.org. Version 2.2 020 April.
  • 33. Hasenclever D, Diehl V: A prognostic score for advanced Hodgkin’s disease. International Prognostic Factors Project on Advanced Hodgkin’s Disease. N Engl J Med. 1998; 339(21): 1506–1514.
  • 34. Hutchinson RJ, Fryer CJ, Davis PC, et al: MOPP or radiation in addition to ABVD in the treatment of pathologically staged advanced Hodgkin’s disease in children: results of the Children’s Cancer Group Phase III Trial. J Clin Oncol. 1998; 16(3):897–906.
  • 35. Ferme C, Eghbali H, Hagenbeek A, et al. MOPP/ABV hybrid and irradiation in unfavorable supradiaphragmatic clinical stages III Hodgkin’s disease. Comparison of three treatment modalities. Preliminary results of the EORTC-GELA H8U randomized trial in 995 patients. Blood. 000; 96: A576.
  • 36. Fabian CJ, Mansfield CM, Dahlberg S, et al: Low-dose involved field radiation after chemotherapy in advanced Hodgkin disease. A Southwest Oncology Group randomized study. Ann Intern Med. 1994; 120(11): 903–912.
  • 37. Poen JC, Hoppe RT, Horning SJ: High-dose therapy and autologous bone marrow transplantation for relapsed/refractory Hodgkin’s disease: The impact of involved field radiotherapy on patterns of failure and survival. Int J Radiat Oncol Biol Phys. 1996; 36(1):3–12..
APA Cetindag M (2021). Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti. , 115 - 127. 10.5505/aot.2021.82473
Chicago Cetindag Mehmet Faik Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti. (2021): 115 - 127. 10.5505/aot.2021.82473
MLA Cetindag Mehmet Faik Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti. , 2021, ss.115 - 127. 10.5505/aot.2021.82473
AMA Cetindag M Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti. . 2021; 115 - 127. 10.5505/aot.2021.82473
Vancouver Cetindag M Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti. . 2021; 115 - 127. 10.5505/aot.2021.82473
IEEE Cetindag M "Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti." , ss.115 - 127, 2021. 10.5505/aot.2021.82473
ISNAD Cetindag, Mehmet Faik. "Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti". (2021), 115-127. https://doi.org/10.5505/aot.2021.82473
APA Cetindag M (2021). Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti. ACTA ONCOLOGICA TURCICA, 54(1), 115 - 127. 10.5505/aot.2021.82473
Chicago Cetindag Mehmet Faik Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti. ACTA ONCOLOGICA TURCICA 54, no.1 (2021): 115 - 127. 10.5505/aot.2021.82473
MLA Cetindag Mehmet Faik Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti. ACTA ONCOLOGICA TURCICA, vol.54, no.1, 2021, ss.115 - 127. 10.5505/aot.2021.82473
AMA Cetindag M Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti. ACTA ONCOLOGICA TURCICA. 2021; 54(1): 115 - 127. 10.5505/aot.2021.82473
Vancouver Cetindag M Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti. ACTA ONCOLOGICA TURCICA. 2021; 54(1): 115 - 127. 10.5505/aot.2021.82473
IEEE Cetindag M "Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti." ACTA ONCOLOGICA TURCICA, 54, ss.115 - 127, 2021. 10.5505/aot.2021.82473
ISNAD Cetindag, Mehmet Faik. "Hodgkin Lenfoma Tedavisi; Son 30 Yılda Neler Değişti". ACTA ONCOLOGICA TURCICA 54/1 (2021), 115-127. https://doi.org/10.5505/aot.2021.82473