Reduced-intensity chemotherapy and PET-guided radiotherapy in patients with advanced stage Hodgkin's lymphoma (HD15 trial): a randomised, open-label, phase 3 non-inferiority trial

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ENGERT Andreas HAVERKAMP Heinz KOBE Carsten MARKOVA Jana RENNER Christoph HO Antony ZIJLSTRA Josee KRÁL Zdeněk FUCHS Michael HALLEK Michael KANZ Lothar DOEHNER Hartmut DOERKEN Bernd ENGEL Nicole TOPP Max KLUTMANN Susanne AMTHAUER Holger BOCKISCH Andreas KLUGE Regine KRATOCHWIL Clemens SCHOBER Otmar GREIL Richard ANDREESEN Reinhard KNEBA Michael PFREUNDSCHUH Michael STEIN Harald EICH Hans Theodor MUELLER Rolf-Peter DIETLEIN Markus BORCHMANN Peter DIEHL Volker

Rok publikování 2012
Druh Článek v odborném periodiku
Časopis / Zdroj Lancet
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
Doi http://dx.doi.org/10.1016/S0140-6736(11)61940-5
Obor Onkologie a hematologie
Klíčová slova POSITRON-EMISSION-TOMOGRAPHY; MOPP/ABV HYBRID; INTERGROUP TRIAL; PROGNOSTIC SCORE; DISEASE PATIENTS; STANFORD-V; ABVD; RISK; COMBINATIONS; PROGRESSION
Popis Background The intensity of chemotherapy and need for additional radiotherapy in patients with advanced stage Hodgkin's lymphoma has been unclear. We did a prospective randomised clinical trial comparing two reduced-intensity chemotherapy variants with our previous standard regimen. Chemotherapy was followed by PET-guided radiotherapy. Methods In this parallel group, open-label, multicentre, non-inferiority trial (HD15), 2182 patients with newly diagnosed advanced stage Hodgkin's lymphoma aged 18-60 years were randomly assigned to receive either eight cycles of BEACOPP(escalated) (8xB(esc) group), six cycles of BEACOPP(escalated) (6xB(esc) group), or eight cycles of BEACOPP(14) (8xB(14) group). Randomisation (1:1:1) was done centrally by stratified minimisation. Non-inferiority of the primary endpoint, freedom from treatment failure, was assessed using repeated CIs for the hazard ratio (HR) according to the intention-to-treat principle. Patients with a persistent mass after chemotherapy measuring 2.5 cm or larger and positive on PET scan received additional radiotherapy with 30 Gy; the negative predictive value for tumour recurrence of PET at 12 months was an independent endpoint. This trial is registered with Current Controlled Trials, number ISRCTN32443041. Findings Of the 2182 patients enrolled in the study, 2126 patients were included in the intention-to-treat analysis set, 705 in the 8xB(esc) group, 711 in the 6xB(esc) group, and 710 in the 8xB(14) group. Freedom from treatment failure was sequentially non-inferior for the 6xB(esc) and 8xB(14) groups as compared with 8xB(esc). 5-year freedom from treatment failure rates were 84.4% (97.5% CI 81.0-87.7) for the 8xB(esc) group, 89.3% (86.5-92.1) for 6xB(esc) group, and 85.4% (82.1-88.7) for the 8xB(14) group (97.5% CI for difference between 6xB(esc) and 8xB(esc) was 0.5-9.3). Overall survival in the three groups was 91.9%, 95.3%, and 94.5% respectively, and was significantly better with 6xB(esc) than with 8xB(esc) (97.5% CI 0.2-6.5). The 8xB(esc) group showed a higher mortality (7.5%) than the 6xB(esc) (4.6%) and 8xB(14) (5.2%) groups, mainly due to differences in treatment-related events (2.1%, 0.8%, and 0.8%, respectively) and secondary malignancies (1.8%, 0.7%, and 1.1%, respectively). The negative predictive value for PET at 12 months was 94.1% (95% CI 92.1-96.1); and 225 (11%) of 2126 patients received additional radiotherapy. Interpretation Treatment with six cycles of BEACOPP(escalated) followed by PET-guided radiotherapy was more effective in terms of freedom from treatment failure and less toxic than eight cycles of the same chemotherapy regimen. Thus, six cycles of BEACOPP(escalated) should be the treatment of choice for advanced stage Hodgkin's lymphoma. PET done after chemotherapy can guide the need for additional radiotherapy in this setting.

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