Skip to main content
Log in

PET beim Hodgkin-Lymphom

Verbessert die Positronenemissionstomographie die Behandlung?

PET in Hodgkin’s lymphoma

Can positron emission tomography improve the therapy?

  • Leitthema
  • Published:
Der Onkologe Aims and scope

Zusammenfassung

Wenn die FDG-PET nach 2 Zyklen Chemotherapie (Interim-PET) negativ ist, entwickelt sich nur selten ein Rezidiv. Daraus folgt ein hoher negativer prognostischer Wert der FDG-PET im Therapiemonitoring des Hodgkin-Lymphoms. Der Schritt zur responseadaptierten Therapie (Therapie-Deeskalation) mittels Interim-PET sollte in Therapieoptimierungsstudien wissenschaftlich begleitet werden. Dies erhöht die Patientensicherheit und sollte eine Referenzbegutachtung der Interim-PET einschließen. Nach Abschluss der Chemotherapie konnte in der HD15-Studie der German Hodgkin Study Group (GHSG) ein progressionsfreies Überleben bei 95% der PET-negativen Patienten in partieller Remission gezeigt werden. Bei Verzicht auf eine Strahlentherapie bei Patienten in partieller Remission mit Restgewebe ≥2,5 cm erhöhte sich die Rate an Frührezidiven im Vergleich zur Patientengruppe in kompletter Remission nicht. Das Gesamtüberleben nach 5 Jahren bleibt abzuwarten. Eine solche Therapiekonsequenz muss sich aber stets an der Intensität der zuvor durchgeführten Chemotherapie orientieren.

Abstract

PET-negative patients after 2 cycles of chemotherapy (interim-PET) rarely develop a relapse. Thus, the negative prognostic value of interim-PET in therapy monitoring of Hodgkin’s lymphoma is high. The next clinical step towards response-adapted therapy (therapy de-escalation) using interim-PET should be embedded in clinical trials and scientific evaluation. This increases the safety for the patients and PET should be evaluated by a second reader. After completion of chemotherapy the progression-free survival was 95% for PET-negative patients in partial remission, as shown in the HD15 trial of the German Hodgkin Study Group (GHSG). Thus, consolidation radiotherapy can be omitted in PET patients with residual tissue of ≥2.5 cm without increasing the risk for progression or early relapse as compared to patients in complete remission. The impact of this finding on the overall survival at 5 years must be awaited. However, such therapy consequences must always be oriented to the intensity of the preceding chemotherapy.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Abb. 1
Abb. 2
Abb. 3
Abb. 4
Abb. 5
Abb. 6
Abb. 7
Abb. 8

Literatur

  1. Aleman BM, Belt-Dusebout AW van den, Klokman WJ et al (2003) Long-term cause-specific mortality of patients treated for Hodgkin’s disease. J Clin Oncol 21:3431–3439

    Article  PubMed  Google Scholar 

  2. Avigdor A, Bulvik S, Levi I et al (2009) Two cycles of escalated BEACOPP followed by four cycles of ABVD utilizing early-interim PET/CT scan is an effective regime for advanced high-risk Hodgkin’s lymphoma. Ann Oncol doi10.1093/annonc/mdp271

  3. Cheson BD, Pfistner B, Juweid ME et al (2007) Revised response criteria for malignant lymphoma. J Clin Oncol 25:579–586

    Article  PubMed  Google Scholar 

  4. Dann EJ, Bar-Shalom R, Tamir A et al (2007) Risk-adapted BEACOPP regimen can reduce the cumulative dose of chemotherapy for standard and high-risk Hodgkin lymphoma with no impairment of outcome. Blood 109:905–909

    Article  CAS  PubMed  Google Scholar 

  5. Wit M de, Bohuslavizki KH, Buchert R et al (2001) 18FDG-PET following treatment as valid predictor for disease-free survival in Hodgkin’s lymphoma. Ann Oncol 12:29–37

    Article  PubMed  Google Scholar 

  6. Diehl V, Franklin J, Pfreundschuh M 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

    Article  CAS  PubMed  Google Scholar 

  7. Gallamini A, Rigacci L, Merli F et al (2006) The predicive value of positron emission tomography scanning performed after two courses of standard therapy on treatment outcome in advanced stage Hodgkin’s lymphoma. Haematologica 91:475–481

    PubMed  Google Scholar 

  8. Gallamini A, Hutchings M, Rigacci L et al (2007) Early interim 2-[18F]-fluoro-2-deoxy-D-glucose positron emission tomography is prognostically superior to international prognostic score in advanced-stage Hodgkin’s lymphoma: a report from a joint Italian-Danish study. J Clin Oncol 25:3746–3752

    Article  CAS  PubMed  Google Scholar 

  9. Hutchings M, Mikhaeel NG, Fields PA et al (2005) Prognostic value of interim PET after two or three cycles of chemotherapy in Hodgkin lymphoma. Ann Oncol 16:1160–1168

    Article  CAS  PubMed  Google Scholar 

  10. Hutchings M, Loft A, Hansen M et al (2006) FDG-PET after two cycles of chemotherapy predicts treatment failure and progression-free survival in Hodgkin Lymphoma. Blood 107:52–59

    Article  CAS  PubMed  Google Scholar 

  11. Hutchings M, Loft A, Hansen M et al (2006) Positron emission tomography with or without computed tomography in the primary staging of Hodgkin’s lymphoma. Haematologica 91:482–489

    PubMed  Google Scholar 

  12. Hutchings M, Loft A, Hansen M et al (2007) Clinical impact of FDG-PET/CT in the planning of radiotherapy for early-stage Hodgkin lymphoma. Eur J Haematol 78:206–212

    Article  PubMed  Google Scholar 

  13. Hutchings M, Barrington SF (2009) PET/CT for therapy response assessment in lymphoma. J Nucl Med 50:21S–30S

    Article  CAS  PubMed  Google Scholar 

  14. Jerusalem G, Beguin Y, Fassotte MF et al (2003) Early detection of relapse by whole-body emission tomography in the follow-up of patients with Hodgkin’s disease. Ann Oncol 14:123–130

    Article  CAS  PubMed  Google Scholar 

  15. Juweid ME, Stroobants S, Hoekstra OS et al (2007) Use of positron emission tomography for response assessment of lymphoma: consensus of the imaging subcommittee of international harmonization project in lymphoma. J Clin Oncol 25:571–578

    Article  PubMed  Google Scholar 

  16. Kobe C, Dietlein M, Franklin J et al (2008) Positron emission tomography has a high negative predictive value for progression or early relapse for patients with residual disease after first line chemotherapy in advanced-stage Hodgkin Lymphoma. Blood 112:3989–3994

    Article  CAS  PubMed  Google Scholar 

  17. Kobe C, Dietlein M, Mauz-Körholz C et al (2008) FDG-PET in Hodgkin lymphoma. Nuklearmedizin 47:235–238

    CAS  PubMed  Google Scholar 

  18. Körholz D, Claviez A, Hasenclever D et al (2004) The concept of the GPOH-HD 2003 therapy study for pediatric Hodgkin’s disease: evolution in the tradition of the DAL/GPOH studies. Klin Padiatr 216:150–156

    Article  PubMed  Google Scholar 

  19. Markova J, Kobe C, Skopalova M et al (2009) FDG-PET for assessment of early treatment response after 4 cycles of chemotherapy in patients with advanced-stage Hodgkin lymphoma has a high negative predictive value. Ann Oncol 20:1270–1274

    Article  CAS  PubMed  Google Scholar 

  20. Meignan M, Gallamini A, Haioun C (2009) Report on the first international workshop on interim-PET scan im lymphoma. Leuk Lymphoma doi 10.1080/1042890903040048

  21. Naumann R, Beuthien-Baumann B, Reiss A et al (2004) Substantial impact of FDG PET imaging on the therapy decision in patients with early-stage Hodgkin’s lymphoma. Br J Cancer 90:620–625

    Article  CAS  PubMed  Google Scholar 

  22. Pakos EE, Fotopoulos AD, Ioannidis JP et al (2005) 18F-FDG PET for evaluation of bone marrow infiltration in staging of lymphoma: a meta-analysis. J Nucl Med 46:958–963

    PubMed  Google Scholar 

  23. Picardi M, De Renzo A, Pane F et al (2007) Randomized comparison of consolidation radiation versus observation in bulky Hodgkin’s lymphoma with post-chemotherapy negative positron emission tompgraphy scans. Leuk Lymphoma 48:1721–1727

    Article  PubMed  Google Scholar 

  24. Rigacci L, Vitolo U, Nassi L et al (2007) Positron emission tomography in the staging of patients with Hodgkin’s lymphoma. A prospective multicentric study by the Intergruppo Italiano Linfomi. Ann Hematol 86:897–903

    Article  PubMed  Google Scholar 

  25. Spaepen K, Stroobants S, Dupont P et al (2001) Can positron emission tomography with [18F]-fluorodeoxyglucose after first-line treatment distinguish Hodgkin’s disease patients who need additional therapy from others in whom additional therapy would mean avoidable toxicity? Br J Haematol 115:272–278

    Article  CAS  PubMed  Google Scholar 

  26. Weihrauch MR, Re D, Scheidhauer K et al (2001) Thoracic positron emission tomography using 18F-fluorodeoxyglucose for the evaluation of residual mediastinal Hodgkin’s disease. Blood 98:2930–2934

    Article  CAS  PubMed  Google Scholar 

  27. Zinzani PL, Tani M, Fanti S et al (2006) Early positron emission tomography (PET) restaging: a predictive final response in Hodgkin’s disease patients. Ann Oncol 17:1296–1300

    Article  CAS  PubMed  Google Scholar 

  28. Zinzani PL, Stefoni V, Tani M et al (2009) Role of [18F]fluorordeoxyglucose positron emission tomography scan in the follow-up of lymphoma. J Clin Oncol 27:1781–1787

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. Dietlein.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dietlein, M., Eich, H., Fuchs, M. et al. PET beim Hodgkin-Lymphom. Onkologe 16, 18–27 (2010). https://doi.org/10.1007/s00761-009-1767-0

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00761-009-1767-0

Schlüsselwörter

Keywords

Navigation