- Angelo Michele Carella1⇓,
- Monica Bellei2,
- Pauline Brice3,
- Christian Gisselbrecht3,
- Giuseppe Visani4,
- Philippe Colombat5,
- Francesco Fabbiano6,
- Amedea Donelli7,
- Stefano Luminari2,
- Pierre Feugier8,
- Peter Browett9,
- Hans Hagberg10 and
- Massimo Federico2
- 1 Div. Ematologia, A.O.U. San Martino, Genova, Italy
- 2 Oncologia II, Dip. Oncologia ed Ematologia, Univ. Modena e Reggio Emilia, Modena, Italy
- 3 Institut d’Hematologie, Hopital Saint-Louis, Paris, France
- 4 Div. Ematologia, Ospedale San Salvatore, Pesaro, Italy
- 5 Service d’Oncologie Medicale et des Maladies des Sang, Centre Hopital Bretonneau, Tours, France
- 6 Div. Ematologia, Ospedale Cervello, Palermo, Italy
- 7 Ematologia, Dip. Oncologia ed Ematologia, Univ. Modena e Reggio Emilia, Modena, Italy
- 8 Dep. Hematology-Internal Medicine, University Hospital of Nancy, France
- 9 Molecular Hematology and Laboratory Medicine, University Auckland, Auckland, New Zealand
- 10 Departments of Oncology, Radiology, and Clinical Immunology, Uppsala Univ, Uppsala, Sweden
- Correspondence: Angelo Michele Carella, MD, Divisione di Ematologia 1, A.O.U. San Martino, l.go R. Benzi 10, 16132 Genova, Italy. E-mail:
The inclusion of high-dose therapy/autologous stem cell transplantation (HDT/ASCT) in the initial treatment plan for patients with unfavorable Hodgkin’s lymphoma (HL) has been a matter of debate for the last two decades. In 1991, Carella et al.1 published a pilot study of HDT and ASCT in patients with unfavorable HL who had achieved CR with conventional-dose therapy. In an attempt to improve the cure rate of advanced, unfavorable HL and to reduce the risk of relapse after initial response, in April 1993 we started a large co-operative study comparing HDT/ASCT versus conventional chemotherapy (CHT) in patients in CR or PR after four courses of ABVD or other doxorubicin-containing regimens.
Between April 1993 and December 2000, 208 patients were registered on the trial; among these, 163 fully complied with the protocol requests and were randomly assigned to receive HDT plus ASCT (HDT-ASCT Arm, 83 patients) versus four additional courses of the same standard chemotherapy used in the induction phase (CHT Arm, 80 patients). Unfavorable HL was defined using a Strauss-derived system.2 The details relative to patients’ characteristics, entry criteria, treatment protocol and statistical analysis have been previously described.3 At the end of the treatment program, 92% of patients in HDT-ASCT arm and 89% in CHT arm achieved a CR (p=0.6). The 5-year FFS rates were 75% (95% confidence interval [CI], range 65–85) in the HDT-ASCT arm and 82% (95% CI, range 73–90) in the CHT arm (p=0.4). The 5-year OS rates were 88% (95% CI, range 80–96) in the HDT-ASCT arm and 88% (95% CI, range 79–96) in the CHT Arm (p=0.99). The 5-year RFS rates were 88% in the HDT-ASCT arm (95% CI, range 80–96) and 94% in the CHT arm (95% CI, range 88–100), and there was no statistical difference (p=0.3). We now present the updated results of this study after an extended follow-up period of four years (median follow-up of alive patients is currently 107 months, range 9–172). In Table 1 we present a flow diagram showing what became of all the patients assigned to each arm and, finally, 10-year OS, RFS and FFS.
The 10-year OS were 85% (95% CI, range 78–90) and 84% (95% CI, range 77–89) for patients who underwent HDT-ASCT or CHT respectively. Also after an extended follow-up, no significant difference emerged between the two arms (p=0.7) (Figure 1A). Since the Hasenclever prognostic score has emerged to be more robust than the Strauss prognostic system, we also performed the analysis of our data according to the former.4 We compared outcome in the two arms but we found no statistical difference [10 year OS: IPS 0–2 (49 pts.): 98% (ASCT), 84% (CHT), p=0.5; IPS 3–6 (84 pts.): 85% (ASCT), 88% (CHT), p=0.8; 10 year FFS: IPS 0–2 (49 pts.): 84% (ASCT), 75% (CHT), p=0.4; IPS 3–6 (84 pts.): 79% (ASCT), 83% (CHT), p=0.8]. The 10-year FFS was 79% (95% CI, range 72–85) for patients in the HDT-ASCT arm and 75% (95% CI, range 67–82) for patients in the CHT arm (p=0.8) (Figure 1B). No difference in late toxicity was observed between the two groups: overall late toxicity consisted of 2 bone necrosis in the HDT/ASCT arm and 2 second malignancies, (cancer of the testis with gastric metastases and one a MDS/AML). In addition to these failures, 2 patients have died from a second malignancy (both lung cancers), one in each arm.
Therefore, after a median follow-up of 107 months, our data definitely support the view that for patients responding to initial conventional CHT the consolidation with HDT/ASCT is not superior to consolidation with conventional-dose therapy and, most importantly, confirm that HDT/ASCT as consolidation therapy should no longer be offered to these patients.
Another relevant issue of our study was the evaluation of safety of an early use of HDT followed by ASCT. According to published data, 2% of deaths caused by HDT/ASCT toxicity can be expected.5 In the present study, only one toxic death occurred thus confirming the increasing safety of this procedure when performed in the initial course of the disease. Of course, these conclusions refer to a population diagnosed with HL in the pre-FDG-PET era, when the treatment decisions were based on adverse risk factors present at time of diagnosis, before treatment was started. Currently, we have more chance of reducing treatment related toxicities and of avoiding undue treatment in selected groups of patients who can be cured with standard-dose regimens. Using FDG-PET scan in the evaluation of treatment response in HL, the negative predictive value is high (81–100%) showing the ability of FDG-PET to identify patients with excellent prognosis.6–8 To these patients we can reasonably apply the conclusions of our study, that is that they do not benefit from an early intensification with HDT and ASCT. The ongoing worldwide trials will most probably provide a definite answer to the role of early PET in the selection of patients at high risk of relapse candidates for intensification with HDT and ASCT.
Angelo Michele Carella and Massimo Federico contributed equally to this study.
Funding: supported by a grant from “Associazione Angela Serra per la Ricerca sul Cancro,” Modena, Italy.
- Copyright© 2009 Ferrata Storti Foundation