Single or Tandem Autologous Stem-Cell Transplantation Given According to Prognostic Factors at Relapse for Hodgkin Lymphoma.

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 2069-2069
Author(s):  
Pauline Brice ◽  
Franck Morschhauser ◽  
Marine Divine ◽  
Christophe Ferme ◽  
Gilles Salles

Abstract Patients with relapsed hodgkin lymphoma (HL)have a different prognostic after high-dose therapy (HDT)according to time to relapse and extend of relapse. From 1995 to 1997, 48 patients with early relapse or refractory HL were included in a pilot study of tandem transplantation to evaluate the feasibility before the protocol. From 1998 to 2002, 200 patients with refractory disease or first relapse of HL were prospectively treated with induction chemotherapy followed by HDT and autologous stem-cell transplantation (ASCT). Patients were stratified in 2 groups according to prognostic factors at relapse: groupe 1 (unfavorable relapse: primary refractory disease or early/disseminated relapse) and group 2 (favorable relapse: patients with either early or disseminated relapse). Induction chemotherapy consisted of ifosfamide/etoposide with doxorubicin (IVA) in 70% of patients or with vinorelbine and mitoguazone (MINE)for the remainings. Group 1, patients received 2 cycles of chemotherapy, PBSC collection and tandem ASCT, with a CBV mitoxantrone (30 mg/m2) and 2 months later cytarabine (6g/m2), melphalan (140mg/m2)with total body irradiation (40%) or busulfan (12 mg/kg) followed by the second ASCT. Group 2, patients received 3 cycles of chemotherapy, PBSC collection and a BEAM regimen followed by ASCT. Final results, updated, January 2005 are presented with 245 evaluable patients. Results: after induction chemotherapy overall response rate was at 61% in group 1 and 96% in group 2. In group 1, 70% received the two ASCT, the major reason not to receive the procedure was disease progression after induction chemotherapy (10%) or after the first ASCT (15%), than low stem-cell collection (4%) or toxicity (2%). In group 2, 97% of patients received ASCT and 1 patient received a tandem ASCT for refractory relapse. 5 patients died from toxicity in group1 and none in group2, but 2 secondary leukemia were observed in this group. In intent to treat analysis, at a 3 years median follow-up from the relapse, the EFS was at 45% in group 1 versus 75% in group 2 and the survival at 55% in group 1 versus 80% in group 2. Despite a different consolidation between group 1 and 2, results remained better in group 2. In conclusion, these results confirmed the importance of prognostic factors at relapse of HL.No differences were found in the unfavorable group 1 between refractory patients and early/disseminated relapse. HL patients with adverse prognostic factors (group 1) but responding to second line chemotherapy and eligible for tandem ASCT may benefit from this procedure with an EFS at 70%. The major cause of failure was chemoresistance either at induction or after high-dose therapy.

Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 4388-4388
Author(s):  
Nicolas Novitzky ◽  
Cecile E. Du Toit ◽  
Andrew B. McDonald

Abstract Introduction: The optimal schedule for the treatment of AML remains to be defined. No systematic analysis of the dose intensity of anthracycline agents during induction chemotherapy has been published. We have compared the outcome of 2 consecutive protocols where daunorubicin was given at two different dose intensities. Methods and patients: Consecutive patients with AML younger than 60 years and who had adequate organ function and were HIV non reactive were entered into a prospective study. Induction therapy included etoposide 100 mg/m2 (for 7 days), cytarabine 100 mg/m2 (as infusion for 7 days) and daunorubicin 75 mg/m2 (for 3 days) followed by one similar consolidation course where daunorubicin was reduced to 60 mg/ (for 3 days) (Group 1). Patients remaining in CR were offered autologous or allogeneic stem cell transplantation (if HLA donor available). They were compared to a previous cohort (Group 2; 1993–1998) who had received similar combination therapy but Daunorubicin was given at 45 mg/m2 and was followed by 2 consolidation courses. Group 2 patients achieving CR were also offered high dose therapy and stem cell grafts. Results: Seventy one individuals (Group 1) with AML with median age of 36 years (14–60) were studied. Fourteen had favourable cytogenetics but had other adverse prognostic factors; 22 had intermediate risk while 16 had adverse karyotypes and no results were available in 20 cases. Three patients had biphenotypic leukaemia. Circulating blast count greater than 50x109/L was present in 17 individuals. Remission was achieved in 80% (57 patients; 8 after 2 courses). Four patients did not receive consolidation because they had persistent fungal infection (n=2), cardiotoxicity (n=1) or refusal. Reduction in cardiac ejection fraction was seen in 3 individuals. Thirty nine patients underwent autologous (n=17) or allogeneic stem cell transplantation (n=22). At median follow up of 338 days, 39% survive disease free. Only two individuals of 19 who achieved CR but did not receive high dose therapy is alive (p < 0.05). Unfavourable cytogenetics but not older age (above median) was associated with adverse outcome. Kaplan and Meier analysis showed superior survival was associated with Allogeneic SCT (73%) than autologous (58%; p= 0.08). Patients in the historical control fraction, (Group 2) had no significant pre-treatment differences with Group 1. Remission in Group 2 was achieved in 59% (p= 0.03). CR occurred with a single course in 86% vs. 64% (p= 0.02) respectively. There were no differences in the toxicity profile between these two combinations. Disease recurred in 28% and 50% (p= 0.07) patients. For the 142 individuals, median follow up is 254 (range 19–4451) and 453 (12–1702; p= 0.01) days. Survival is 23% and 39% respectively, favouring patients treated in Group 1 (Log Rank; p= 0.03). Conclusions: We conclude that increasing daunorubicin during induction chemotherapy was not associated with excessive toxicity, while remission rates were of 80% and 58%. However, a particularly favourable outcome was seen in patients receiving allogeneic stem cell transplantation.


2019 ◽  
pp. 1-6 ◽  
Author(s):  
Rabia Wali ◽  
Haleema Saeed ◽  
Naveed Patrus ◽  
Shehla Javed ◽  
Saadiya Javed Khan

PURPOSE Hodgkin lymphoma is the most common cancer in children, adolescents, and young adults. Overall survival is approximately 80% to 90%. A subset of these patients has refractory disease or experience disease relapse. Conventional salvage therapies and autologous stem-cell transplantation is usually considered the standard of care for these patients. Our analysis reports outcomes in these patients. PATIENTS AND METHODS After institutional review board approval, a retrospective analysis of patients with Hodgkin lymphoma who were up to 18 years of age and who had refractory or relapsed disease at Shaukat Khanum Memorial Cancer Hospital and Research Centre from September 2009 to December 2013 was performed. Patients who underwent high-dose chemotherapy followed by stem-cell rescue were included in this analysis. RESULTS A total of 567 patients with Hodgkin lymphoma registered at the hospital. Sixty of the patients (10.6%) had either primary progressive or refractory disease or relapse after finishing with first-line chemotherapy. High-dose chemotherapy followed by stem cell was administered to 25 of these patients (42%). Thirteen patients (40%) had progressive disease (PD), five (22%) had early relapse, and seven (38%) had late relapse. A number of salvage regimens were used, including etoposide, prednisolone, ifosfamide, and cisplatin; dexamethasone, cytarabine, and carboplatin; and gemcitabine plus vinorelbine. Re-evaluation was performed before taking patients to a high dose, and it showed complete response in 17 patients (68%), partial response in six patients (24%), and PD in two patients (8%). Twenty-one patients (84%) are in remission after transplantation, with two patients (8%) having died as a result of disease progression and two patients (2%) having relapsed after treatment. Overall survival is 92% at 4 years, with event-free survival of 80% at 4 years. CONCLUSION Our retrospective analysis shows good outcomes in patients who had PD or refractory disease. Disease response before transplantation is important in predicting outcomes.


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