Despite the mature results of the new intensive treatments, ABVD is still considered the standard therapy of the HL. Here we report the 2-year results of a phase 2 study which explore the possibility to ameliorate the performance of this (g)old schedule. Primary End-Points: CR and early cardio-toxicity. Secondary End-Points: survival (FFP,OS) and late cardio-toxicity. 23/25 CR (CI 90%) to validate the study (80% standard vs 90% DD-DI ABVD, CI +/− 10% one tail test, 5% sig stat level). Modifications of the standard (st) ABVD and strategy concepts are summarized as follow:

  1. Each patient received a total of 6 cycles without RT

  2. Adryamicin (ADM) was escalated from 50 to 70 mg/m2 in the cycles 1,2,3,4. The cumulative dose of ADM was 380 mg/m2.

  3. The intercycle period was shortened from 28 to 21 days for all 6 cycles; the 4 drugs were delivered at day 1 and 11 of each cycle

  4. G-CSF was given from d4 to d8, and from d14 to d18 of each cycle

  5. The therapy program was driven by dynamic indicators such as interim-PET and CT fusion images.

  6. Normalisation of PET images at the end of 2nd cycles was indicator of early CR, while the persistence of PET+ lesion(s) at the end of the 4th cycle was indicator of failure and consequently the treatment was shift to a high-dose CT/CD34+ rescue program.

  7. RT was eliminated. At the end of 6th cycle, PET- residual masses were monitored by PET/TC fusion images.

  8. An historical group of 94 HL pts treated with 6–8 cycles of st-ABVD +/− RT was used to compare response, survival and toxicity data.

Compared to st-ABVD the theoretical relative dose-intensity (RDI) values of drugs were 1.86 for ADM, 1.33 for DTIC, Bleomycin and Vinblastine, and 1.46 for the entire schedule. Administered RDIs of the schedule (delivered cycles = 184) ranged between 1.10 to 1.55 (median value 1.39).

Results: from June 2004 to August 2006 thirty-nine pts were enrolled (tab1). As the 8th August 2006 thirty-five out of 39 pts have performed the interim-PET-TC fusion images and thirty-two completed the treatment: 100% of valuable pts obtained the early CR (35/35) and CR (32/32). All pts are alive and free of disease (tab2 and fig.1).

Cardiac functions were monitored by ECG, Ecography, MUGA scan, pro-BNP, and troponin T. Toxicity was mild and similar to standard ABVD.

Dose-dense and dose-intense ABVD is feasible, well tolerated and highly active in newly diagnosed patients with advanced/intermediated Hodgkin’s lymphoma: six cycles without RT seem superior to 6–8 cycles of ABVD +/− RT (fig 1) and may be a promising program for optimal long-term results.

tab1

presentation features

Features
total 39 100% 
Early unfavourable 23% 
Advanced 30 77% 
Age > 45 –yr 10% 
Bulky 19 44% 
Stage IV 13 33% 
B symptoms 25 64% 
Extranodal 23% 
VES > 50 mm 20 51% 
LDH Ratio > 1 15 38% 
IPS ≥ 3 10 26% 
N. Sites>3 28 72% 
Male 13 33% 
Features
total 39 100% 
Early unfavourable 23% 
Advanced 30 77% 
Age > 45 –yr 10% 
Bulky 19 44% 
Stage IV 13 33% 
B symptoms 25 64% 
Extranodal 23% 
VES > 50 mm 20 51% 
LDH Ratio > 1 15 38% 
IPS ≥ 3 10 26% 
N. Sites>3 28 72% 
Male 13 33% 
tab.2

Response and Survival

N. of patientspercent
*n°. of valuable pts as 8 August 2006 
Early CR 35/35* 100% 
CR 32/32* 100% 
FFP-2yr 32/32* 100% 
OS-2yr 32/32* 100% 
N. of patientspercent
*n°. of valuable pts as 8 August 2006 
Early CR 35/35* 100% 
CR 32/32* 100% 
FFP-2yr 32/32* 100% 
OS-2yr 32/32* 100% 

Freedom From Progression

Freedom From Progression

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Disclosure: No relevant conflicts of interest to declare.

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