Klin Padiatr 2020; 232(02): 106
DOI: 10.1055/s-0040-1701897
PW VI-X
Guided Poster Walk
© Georg Thieme Verlag KG Stuttgart · New York

PW VI-X-01 Relapse-localization in pediatric patients with Hodgkin lymphoma

AY Lundgaard
1   Department of Oncology, University of Copenhagen, Rigshospitalet, Copenhagen, Denmark
,
LL Hjalgrim
2   Department of Pediatric Haematology and Oncology, University of Copenhagen, Rigshospitalet, Copenhagen, Denmark
,
AK Berthelsen
1   Department of Oncology, University of Copenhagen, Rigshospitalet, Copenhagen, Denmark
3   Department of Clinical Physiology, Nuclear Medicine and PET, University of Copenhagen, Rigshospitalet, Copenhagen, Denmark
,
L Specht
1   Department of Oncology, University of Copenhagen, Rigshospitalet, Copenhagen, Denmark
,
L Borgwardt
3   Department of Clinical Physiology, Nuclear Medicine and PET, University of Copenhagen, Rigshospitalet, Copenhagen, Denmark
,
MV Maraldo
1   Department of Oncology, University of Copenhagen, Rigshospitalet, Copenhagen, Denmark
› Author Affiliations
Further Information

Publication History

Publication Date:
18 March 2020 (online)

 
 

Introduction Radiotherapy (RT) is the single most effective modality to achieve local control of Hodgkin lymphoma (HL) [1]. However, large treatment fields of the past are associated with an increased morbidity and mortality in long-term survivors [2]. In the management of pediatric patients with HL (pHL), recent treatment protocols use a response-based approach to achieve omission of consolidating RT following combination chemotherapy due to the risk of late toxicity. Event-free survival rates decrease with up to 10% when RT is omitted, but salvage treatment is effective and overall survival rates are similar so far [3] [4]. However, intensive salvage treatment is also associated with significant late effects. It is recognized that most relapses occur within the initially involved sites if RT is not used [5]. Here, we analyze the relapse-localization relative to the initially involved site, and if irradiated, to the irradiated site in pHL.

Methods The Danish Childhood Cancer Registry was used to identify children diagnosed with HL and those who relapsed from 1990–2018 at two institutions. Patient characteristics, treatment details (including RT plans), and diagnostic imaging were collected. We merged scans from the time of diagnosis and the time of relapse using the Eclipse treatment planning system (Varian Medical Systems) and visually assessed the relapse-localization relative to the initially involved site and, if irradiated, the irradiated site.

Results A total of 130 children were diagnosed with HL and 18 relapses were registered. Out of 18 patients 3 had refractory disease resulting in 15 relapses and a crude relapse-rate of 11.5%. The patients’ median age at time of diagnosis was 13 years (range 5–17) and the median time to relapse was 6 months (range 2–59). Out of 15 patients 14 relapsed within the initially involved site. Six patients had received RT and 5 relapsed within both the initially involved and irradiated site (3 single site, 2 multiple sites). One patient relapsed outside of both the initially involved site and the irradiated site. Out of 5 patients with initially bulky disease, 2 relapsed within (no RT) and 3 relapsed outside (2 irradiated, 1 not) the site of bulky disease.

Conclusion It is reasonable to conclude that most relapses occur within the initially involved sites, and that RT improves local control. However, the number of relapses is small, and it is difficult to draw conclusions regarding the relapse pattern. Relapses-localization in pHL from all of Denmark will be analyzed.


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Conflict of Interest:

The authors report no conflicts of interest.

  • References

  • 1 Specht L. Radiotherapy for Hodgkin Lymphoma. Cancer J. 2018; 24 (05) : 237-243 .
  • 2 Castellino SM, Geiger AM, Mertens AC. , et al. Morbidity and mortality in long-term survivors of Hodgkin lymphoma: a report from the Childhood Cancer Survivor Study. Blood. 2011; 117 (06) : 1806-1816 .
  • 3 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 .
  • 4 Wolden SL, Chen L, Kelly KM. , et al. Long-term results of CCG 5942: a randomized comparison of chemotherapy with and without radiotherapy for children with Hodgkin’s lymphoma–a report from the Children’s Oncology Group. J Clin Oncol. 2012; 30 (26) : 3174-3180 .
  • 5 Krasin MJ, Rai SN, Kun LE. , et al. Patterns of Treatment Failure in Pediatric and Young Adult Patients With Hodgkin’s Disease: Local Disease Control With Combined-Modality Therapy. J Clin Oncol. 2005; 23 (33) : 8406-8413 .

  • References

  • 1 Specht L. Radiotherapy for Hodgkin Lymphoma. Cancer J. 2018; 24 (05) : 237-243 .
  • 2 Castellino SM, Geiger AM, Mertens AC. , et al. Morbidity and mortality in long-term survivors of Hodgkin lymphoma: a report from the Childhood Cancer Survivor Study. Blood. 2011; 117 (06) : 1806-1816 .
  • 3 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 .
  • 4 Wolden SL, Chen L, Kelly KM. , et al. Long-term results of CCG 5942: a randomized comparison of chemotherapy with and without radiotherapy for children with Hodgkin’s lymphoma–a report from the Children’s Oncology Group. J Clin Oncol. 2012; 30 (26) : 3174-3180 .
  • 5 Krasin MJ, Rai SN, Kun LE. , et al. Patterns of Treatment Failure in Pediatric and Young Adult Patients With Hodgkin’s Disease: Local Disease Control With Combined-Modality Therapy. J Clin Oncol. 2005; 23 (33) : 8406-8413 .