Ifosfamide, gemcitabine, and vinorelbine: a new induction regimen for refractory and relapsed Hodgkin’s lymphoma
Armando Santoro, Massimo Magagnoli, Michele Spina, Graziella Pinotti, Licia Siracusano, Mariagrazia Michieli, Andrea Nozza, Barbara Sarina, Emanuela Morenghi, Luca Castagna, Umberto Tirelli, Monica Balzarotti
Haematologica January 2007 92: 35-41; doi:10.3324/haematol.10661

Author Affiliations

  1. Armando Santoro⇓,
  2. Massimo Magagnoli,
  3. Michele Spina,
  4. Graziella Pinotti,
  5. Licia Siracusano,
  6. Mariagrazia Michieli,
  7. Andrea Nozza,
  8. Barbara Sarina,
  9. Emanuela Morenghi,
  10. Luca Castagna,
  11. Umberto Tirelli and
  12. Monica Balzarotti
  1. From the Department of Medical Oncology and Hematology, Istituto Clinico Humanitas, Rozzano, Italy (AS, MM, LS, AN, BS, EM, LC, MB), Department of Medical Oncology, Centro di Riferimento Oncologico, Aviano, Italy (MS, MM, UT), Division of Medical Oncology, Ospedale di Circolo, Varese, Italy (GP)
  1. Correspondence: Armando Santoro, M.D., Department of Medical Oncology and Hematology, Istituto Clinico Humanitas, via Manzoni 56, 20089 Rozzano, Milan, Italy. E-mail: armando.santoro{at}humanitas.it
View Abstract

Abstract

Background and Objectives Response to pre-transplant salvage chemotherapy remains the most important prognostic factor for outcome in refractory or relapsed Hodgkin’s lymphoma. Results of a new induction regimen are reported in terms of response rates, toxicity, and stem cell mobilization.

Design and Methods Ninety-one patients with refractory or relapsed Hodgkin’s lymphoma were treated prospectively with a salvage regimen consisting of ifosfamide 2000 mg/m2 on days 1 to 4, gemcitabine 800 mg/m2 on days 1 and 4, vinorelbine 20 mg/m2 on day 1, and prednisolone 100 mg on days 1 to 4 (IGEV).

Results Forty-nine patients (53.8%) achieved a complete remission and 25 (27.5%) a partial response for an overall response rate of 81.3%. In the multivariate analysis response to the last chemotherapy (p<0.0001) and involvement of ≥3 sites (p<0.049) were the most important prognostic factors for response. Adequate CD34+ cell collection was achieved in 78 out of 79 (98.7%) mobilized patients. So far, no treatment-related death has been documented. Thirteen (4.2%) and 27 (8.6%) out of 313 evaluated cycles had to be delayed or reduced, respectively, mainly because of neutropenia and thrombocytopenia. No grade 4 non-hematologic toxicity was observed, except for one episode of mucositis.

Interpretation and Conclusions The high response rate, in particular the complete remission rate, the low toxicity profile, and the very high mobilizing potential of the IGEV regimen strongly suggest that patients with relapsed/refractory Hodgkin’s lymphoma may benefit from the use of this salvage induction regimen.

Since the early 1990s, salvage chemotherapy followed by high dose chemotherapy with autologous bone marrow or peripheral blood stem cell (PBSC) support has become the gold standard treatment for patients with refractory or relapsed Hodgkin’s lymphoma, as clearly shown by several retrospective or phase II studies,1,2 as well as by two prospective randomized trials.3,4 This treatment approach can produce long-term remissions in approximately 40–50% of relapsed patients,5–7 and in up to 25–30% of those with primary refractory disease.8–11 The possibility of a cure depends strongly on several prognostic factors, including duration of the initial remission, extent of disease, prior chemotherapy regimen, presence of B symptoms, and the number of previous chemotherapy lines.2,5,12–15 However, in almost all series, the disease status before high-dose chemotherapy with PBSC support remains the most important factor predicting outcome for these patients.2,4–5, 13–15

Very few studies reported data relating to which standard-dose salvage regimen is the best to induce a good clinical response and shrinkage of bulky disease16 –25 before high-dose therapy. Hence, the identification of new active regimens, combining therapeutic activity and CD34+ stem cell mobilizing potential, is of the utmost importance to increase pre-transplant response rates and, possibly, the final outcome.

In November 1997, following initial experiences with single-agent vinorelbine26 and gemcitabine,27 as well as with a combination of vinorelbine and ifosfamide, 24,28 we designed a new chemotherapy regimen including gemcitabine, vinorelbine, and ifosfamide for patients with refractory or relapsed Hodgkin’s lymphoma. This combination was used in a multicenter study whose results with regards to response rates, toxicity, and stem cell mobilization are reported here.

Design and Methods

Study design

From November 1997 to September 2005, 91 patients with relapsed or primary refractory Hodgkin’s lymphoma after chemotherapy with or without radiotherapy were entered in a study protocol consisting of four cycles of combined ifosfamide, gemcitabine, and vinorelbine (IGEV).The protocol was approved by the Ethics Committee and written informed consent was obtained from all participants. Patients who had failed to achieve complete remission with previous chemotherapy were defined as refractory, those who relapsed after an initial complete remission were classified as having relapsed.

All patients were staged according to the Cotswolds modification of the Ann Arbor system and all underwent at least computed tomography of the thorax and abdomen, and bone marrow biopsy. Starting from 2002, many patients underwent positron emission tomography (PET)-scanning as part of thier staging procedure. Other criteria for eligibility were World Health Organization (WHO) performance status ≤2, and adequate pulmonary, cardiac, renal, and liver function. Human immunodeficiency virus-positive patients were excluded.

Bulky disease was defined as a mediastinal mass larger than one third of the maximum thoracic diameter and/or any node over 10 cm. Disease evaluation was performed after two and four chemotherapy cycles by repeating all examinations that had given an initial positive response. Bone marrow biopsy was repeated when initially positive.

Therapy

The IGEV regimen was administered in an outpatient setting. This regimen consists of ifosfamide 2000 mg/m2 on days 1 to 4 as a 2-hour infusion/day with 2,000 mL saline solution hyperhydration, MESNA 2600 mg/m2 on days 1 to 4, gemcitabine 800 mg/m2 on days 1 and 4, vinorelbine 20 mg/m2 on day 1, and prednisolone 100 mg on days 1 to 4, of each 3-week course. Granulocyte colony-stimulating factor (G-CSF) was administered from day 7 to day 12 of each course or up to apheresis in the course of mobilization. Four courses of chemotherapy were planned, provided there was evidence of at least partial remission after the second cycle. PBSC were collected after the first or second course in the first 11 patients, in order to test the mobilizing potential of the regimen, and thereafter after the third treatment course whenever an objective response was observed. A target yield of at least 3.0 × 106 CD34+ cells/kg of body weight was planned to support each high-dose chemotherapy. The mobilization procedure was considered to have failed when the target yield was not achieved. Apheresis, CD34+ analysis, and cryopreservation procedures have been reported previously. 27 Patients with complete or partial remission after four IGEV courses received single or tandem high-dose chemotherapy.

Monitoring and toxicity assessment

Just 3 weeks before entering the study, each patient underwent a clinical assessment that included evaluation of B symptoms and WHO performance status score, recording of weight, height, blood pressure, and pulse rate, and measurement of palpable or visually identified tumor lesions. All patients underwent the following tests: complete blood cell counts, blood chemistry, coagulation tests, urine analyses, electrocardiography and echocardiography. During therapy, WHO performance status, weight, blood pressure, pulse rate, and a complete blood cell count were obtained before each course. The toxic effects were evaluated according to the WHO Common Toxicity Criteria. Tumor manifestations were reassessed after the second and fourth treatment cycles using the same baseline imaging technique throughout the study. Bidimensional tumor measurements and response evaluation were based on WHO standard criteria.29 Responses were confirmed on two separate measurements made at least 4 weeks apart. PET negativity was mandatory to define complete remission in those patients initially staged by PET. Time to best response and time to disease progression were measured from the start of IGEV treatment to the time of documentation of response or tumor progression. Survival was calculated from the beginning of therapy to the time of death from any cause.

Statistics

Our analysis included all patients who completed IGEV treatment before November 2005. Data are described as numbers and percentages, or means and standard deviations, when appropriate. The prognostic factors were subjected to univariate logistic regression analysis to determine whether they also influenced the response to IGEV. All variables showing a p value <0.1 were considered as candidates for a stepwise logistic regression procedure. All calculations were performed using Stata 9 software (www.stata.com).

Results

Patients’ characteristics

Ninety-one patients with primary refractory or relapsed Hodgkin’s lymphoma were enrolled and evaluated for response to and toxicity of IGEV. The patients’ main characteristics before the initiation of IGEV chemotherapy are listed in Table 1. There were 52 males and 39 females; their median age was 30 years (range 17–59 years). Nodular sclerosis was the most frequent histological subtype (74.7%). A high percentage of patients had B symptoms (59.3%), extranodal involvement (47.2%), more than three involved sites (45.1%), and/or bulky disease (45.1%). As regards response to the last chemotherapy before IGEV administration, 36 patients (39.6%) were refractory, whereas the remaining 55 patients (60.4%) achieved a complete remission, which lasted less than 12 months in 28, and over 12 months in 27 cases.

View this table:
Table 1.

Response rate as a function of the patients’ characteristics before IGEV chemotherapy.

According to the initial stage of their disease, all patients had received from four to eight courses of at least one previous chemotherapy combination. The majority of patients (76.9%) had received only one regimen, with a range from one to four. All patients had been treated with an anthracycline-containing regimen: 38 with adriamycin, bleomycin, vinblastine, dacarbazine (ABVD); 18 with mechlorethamine, oncovin, procarbazine, prednisolone (MOPP) alternated with ABVD; 29 with epidoxorubicin, cyclophosphamide, vinorelbine, bleomycin, prednisone (VEBEP); and 6 with other regimens. Four patients had relapsed after high-dose chemotherapy with PBSC support. Fifty-five patients had received radiotherapy as part of their previous treatment program for Hodgkin’s lymphoma. The median follow-up time was 26 months, with a range from 5 to 94 months.

Response to IGEV

Forty-nine patients (53.8%) achieved complete remission and 25 (27.5%) partial remission with an overall response rate of 81.3% (Table 1). Prognostic factors influencing the likelihood of patients achieving a response were disease status at accrual (relapsed vs refractory, p<0.001), and previous radiotherapy (p<0.019), while a trend was observed for number of involved sites (p=0.076). All other prognostic factors such as age, B symptoms, histology, extranodal involvement, bulky disease, number of previous chemotherapy regimens, duration of previous complete remission (≤12 months vs >12 months), and previous high-dose chemotherapy with PBSC support, did not influence the response rate significantly.

Prognostic factors associated with response, according to the univariate p<0.1 criterion, were entered into a multivariate logistic regression model (Table 2). The significant predictive factors were response to the last chemotherapy before IGEV (complete remission vs. partial remission vs. induction failure; p<0.0001), and number of involved sites (≤3 vs >3 sites, p=0.049), whereas previous radiotherapy lost significance in multi variate analysis.

View this table:
Table 2.

Multivariate analysis for response.

Overall, 64 out of 74 patients in complete or partial remission after IGEV proceeded to single (29 cases) or tandem (35 cases) high-dose chemotherapy with PBSC support. Another five responsive patients who had been treated with IGEV following relapse after previous high-dose chemotherapy with PBSC were allocated to receive non-myeloablative allogeneic transplants. The remaining five patients refused high-dose therapy. The 3-year freedom from progression and overall survival rates were 52.98% and 70.03%, respectively, for the entire series. However long-term results were influenced by response to previous chemotherapy as well as to the IGEV regimen. Details on freedom from progression and overall survival require a longer follow-up.

Treatment delivery and toxicity

The details on treatment delivery and toxicity are reported in Table 3. No treatment-related deaths have been documented so far. Only one treatment toxicity-related admission to the hospital occurred. Out of 313 cycles evaluated, 13 (4.2%) were delayed and 27 (8.6%) reduced mainly because of neutropenia and thrombocytopenia. Overall, the IGEV-related toxic effects were mild with a relatively low incidence of grade 3 and 4 toxicity according to WHO Common Toxicity Criteria. In particular, grade 4 hematologic toxicity was recorded in a very limited number of cycles. Platelet transfusion support was required in 15 cycles (4.8%), and red blood cells were transfused in 25 cycles (8.0%). As regards non-hematologic toxicity, no grade 4 effects were recorded except for one case of mucositis. No grade 3 or 4 renal, neurological, hepatic, or myocardial function toxicity was observed. Eleven infections (3.5%) were documented; however, all patients recovered quickly. Grade 3 ifosfamide-related cystitis occurred in one case and promptly recovered with hyperhydration and mesna supplementation. In no case was ifosfamide stopped or reduced because of cystitis.

View this table:
Table 3.

Main toxicity according to WHO Common Toxicity Criteria.

Stem cell collection

Seventy-nine patients underwent stem cell mobilization with G-CSF (236 μg/kg per day) from day 7 to leukapheresis after one (4 patients), two (7 patients), three (60 patients) and four (8 patients) IGEV cycles (Table 4). Twelve patients did not undergo stem cell mobilization because of disease progression before the third IGEV cycle (9 cases) or allocation to allogeneic transplantation (3 cases). Leukapheresis was performed when the number of CD34+ cells/mL was at least 12 and conducte daily possibly until over 3 × 106 or 6 × 106 CD34+ cells/kg were collected according to whether single or tandem high-dose chemotherapy procedures were planned. In all cases harvesting started from between day 11 and 17 (median, day 13) following the beginning of IGEV chemotherapy. An adequate CD34+ cell collection (i.e. over 3 × 106 CD34+ cells/kg for each high-dose chemotherapy procedure) was achieved in 78 out of 79 (98.7%) mobilized patients, the only failure pooling 2.3 × 106 CD34+ cells/kg.

View this table:
Table 4.

Peripheral blood stem cell collection.

The median number of CD34+ cells collected was 10.5 × 106/kg (range, 3.0–39.0 × 106/kg) with a median of one (range 1–3) apheresis procedure for patients elegible for single high dose treatment, whereas the median number of CD34+ cells was 10.3 × 106/kg (range, 6.0–22.0 × 106/Kg) with a median of two (range, 1–3) apheresis procedures for candidates for tandem transplant. Overall the target yields of 3 × 106 and 6 × 106 CD34+cells/kg were reached in 69.0% and 44.0% of cases, respectively, after the first apheresis procedure and in 20.7% and 50.0%, after the second apheresis.

Discussion

The response rates to pre-transplant induction chemotherapy regimens and/or their mobilizing potential, as well as their impact on outcome have been assessed accurately in only a small number of studies (Table 5). Usually induction chemotherapy has produced an overall response rate of around 70–80% and the complete remission rate has been lower than 30–35%.

View this table:
Table 5.

Summary of results with pre-transplant salvage regimens

Our study outlines the results of a prospective program evaluating a new chemotherapy regimen (IGEV) for the treatment of 91 patients with refractory/relapsed Hodgkin’s lymphoma. The study regimen, which was based on the results of previous protocols including vinorelbine,26 gemcitabine,27 and ifosfamide plus vinorelbine,24,28 induced an overall response rate of 81.3%, which is comparable to rates reported in the past. However, the incidence of complete remission induced by four courses of IGEV, was very high (53.8%) compared with previous data (Table 5). The complete remission rate in refractory patients (33.3%) is also noteworthy even though it is lower than that observed in relapsed patients (67.3%). As a consequence disease status (i.e. relapsed vs. refractory) disease extent (i.e., number of involved sites before IGEV) remain the most important predictors of response in multivariate analysis.

With regard to toxicity, IGEV was very well tolerated with one hospitalization and no treatment-related deaths. Only a very limited number of cycles had to be delayed because of hematologic or non-hematologic toxicity, and from a general viewpoint toxicity was mild. Grade 4 hematologic toxicity was recorded in a very low number of cycles. Furthermore, no grade 4 extrahematologic toxicity was observed, except for one episode of mucositis, and no patient developed grade 3 toxicity apart from mucositis (1.9% of cycles), cystitis (0.3% of cycles) and nausea and vomiting (3.2% of cycles). These data compare very favorably with those from other series in which a higher incidence of side-effects was documented (Table 5).

Finally the capacity to mobilize PBSC is a critical requirement for a pre-transplant induction regimen. In the majority of previous reports on high-dose chemotherapy, data on CD34+ cell mobilization are lacking and details on PBSC mobilization and collection are reported in a limited number of studies11,23,30–32 (Table 6). An adequate stem cell collection (>2 × 106 CD34+ cells/kg) was observed in over 80% of patients. In the present series, the target yield of 3 × 106 or 6 × 106 CD34+ cells/kg after IGEV was reached in almost all patients (98.7%), with a failed harvest of 2.3 × 106 CD34+ cells in only one patient. Furthermore, a single apheresis procedure was sufficient to achieve the target yield in a high percentage of cases. These data confirm our previous experience with ifosfamide plus vinorelbine28 and are better than those attained with the two widely used regimens: ICE11 and miniBEAM.23

View this table:
Table 6.

Summary of stem cell collection with induction chemotherapy.

In conclusion, our results strongly suggest the benefit of IGEV as a salvage induction regimen in patients with refractory or relapsed Hodgkin’s lymphoma. This is clearly supported by the high response rate, in particular the complete remission rate, the very favorable toxicity profile, and also the very high mobilizing potential.

Acknowledgments

We are very grateful to patients and their families for their participation in the study. We also thank Rita Finotto and Antonietta Del Vecchio for their support in conducting the study

Footnotes

  • Author Contributions

    AS acted as principal investigator: he designed the protocol, co-ordinated the study, and wrote the report. MM, MB, MS, GP, LS, AN, and UT participated in the data collection, analysis and interpretation. IC, MM, and BS provided guidance regarding the interpretation of the study results; EM analyzed the data. The study sponsor had no role in the study design, in the data collection, analysis, and interpretation, or in the writing of the report. The corresponding author had full access to the data and took final responsability to submit this report for publication.

  • Conflict of Interest

    The authors reported no potential conflicts of interest.

  • Received August 16, 2006.
  • Accepted November 8, 2006.

References

  1. ↵
    1. Seyfarth B,
    2. Josting A,
    3. Dreyling M,
    4. Schmitz N
    (2006) Relapse in common lymphoma subtypes: salvage treatment options for follicular lymphoma, diffuse large cell lymphoma and Hodgkin disease. Br J Haematol 133:3–18.
    OpenUrlCrossRefMedlineWeb of Science
  2. ↵
    1. Magagnoli M,
    2. Castagna L,
    3. Balzarotti M,
    4. Demarco M,
    5. Santoro A
    What is the best option to cure patients with resistant/relapse Hodgkin’s disease? Current stem cell research and therapy, Submitted.
  3. ↵
    1. Linch DC,
    2. Winfield D,
    3. Goldstone AH,
    4. Moir D,
    5. Hancock B,
    6. McMillan A,
    7. et al.
    (1993) Dose intensification with autologus bone marrow transplantation in relapsed and resistant Hodgkin’s disease: results of a BNLI randomized trial. Lancet 341:1051–4.
    OpenUrlCrossRefMedlineWeb of Science
  4. ↵
    1. Schmitz N,
    2. Pfistner B,
    3. Sextro M,
    4. Sieber M,
    5. Carella AM,
    6. Haenel M,
    7. et al.
    (2002) German Hodgkin's Lymphoma Study Group; Lymphoma Working Party of the European Group for Blood and Marrow Transplantation. Aggressive conventional chemotherapy compared with high-dose chemotherapy with autologous haemopoietic stem cell transplantation for relapsed chemosensitive Hodgkin’s disease: a randomized trial. Lancet 359:2065–71.
    OpenUrlCrossRefMedlineWeb of Science
  5. ↵
    1. Sureda A,
    2. Arranz R,
    3. Iriondo A,
    4. Carreras E,
    5. Lahuerta JJ,
    6. Garcia-Conde J,
    7. et al.
    (2001) Grupo Espanol de Linfomas/Transplante Autologo de Medula Osea Spanish Co operative Group Autologous stem cell transplantation for Hodgkin’s disease: results and prognostic factors in 494 patients from the Grupo Espanol de Linfomas/Transplante de Medula Osea Spanish cooperative group. J Clin Oncol 19:1395–404.
    OpenUrlAbstract/FREE Full Text
    1. Brice P,
    2. Divine M,
    3. Simon D,
    4. Coiffier B,
    5. Leblond V,
    6. Simon M,
    7. et al.
    (1999) Feasibility of tandem autologous stem-cell transplantation in induction failure or very unfavorable relapse from Hodgkin’s disease. Ann Oncol 10:1485–8.
    OpenUrlAbstract/FREE Full Text
  7. ↵
    1. Sweetenham JW,
    2. Taghipour G,
    3. Milligan D,
    4. Blystad AK,
    5. Caballero D,
    6. Fassas A,
    7. et al.
    (1997) High-dose therapy and autologus stem cell rescue for patients with Hodgkin’s disease in first relapse after chemotherapy: results from the EBMT. Bone Marrow Transplant 20:745–52.
    OpenUrlCrossRefMedlineWeb of Science
  8. ↵
    1. Lazarus HM,
    2. Loberiza FR Jr.,
    3. Zhang MJ,
    4. Armitage JO,
    5. Ballen KK,
    6. Bashey A,
    7. et al.
    (1995) High dose cyclophosphamide, carmustine (BCNU), and etoposide (VP16-213) with or without cisplatin (CBV +/− P) and autologous transplantation for patients with Hodgkin’s disease who fail to enter a complete remission after combination chemotherapy. Blood 86:451–6.
    OpenUrlAbstract/FREE Full Text
    1. Prince HM,
    2. Crump M,
    3. Imrie K,
    4. Stewart AK,
    5. Girouard C,
    6. Brandwein JM,
    7. et al.
    (1996) Intensive therapy and autotransplant for patients with an incomplete response to front line therapy for lymphoma. Ann Oncol 7:1043–9.
    OpenUrlAbstract/FREE Full Text
    1. Lazarus HM,
    2. Rowlings PA,
    3. Zhang MJ,
    4. Vose JM,
    5. Armitage JO,
    6. Bierman PJ,
    7. et al.
    (1999) Autotransplants for Hodgkin’s disease in patients never achieving remission: a report from the Autologous Blood and Marrow Transplant Registry. J Clin Oncol 17:534–45.
    OpenUrlAbstract/FREE Full Text
  11. ↵
    1. Moskowitz CH,
    2. Kewalramani T,
    3. Nimer SD,
    4. Gonzalez M,
    5. Zelenetz AD,
    6. Yahalom J
    (2004) Effectiveness of high dose chemoradiotherapy and autologous stem cell transplantation for patients with biopsy-proven primary refractory Hodgkin’s disease. Br J Haematol 124:645–52.
    OpenUrlCrossRefMedlineWeb of Science
  12. ↵
    1. Bonfante V,
    2. Santoro A,
    3. Viviani S,
    4. Devizzi L,
    5. Balzarotti M,
    6. Soncini F,
    7. et al.
    (1997) Outcome of patients with Hodgkin’s disease failing after primary MOPP-ABVD. J Clin Oncol 15:528–34.
    OpenUrlAbstract/FREE Full Text
  13. ↵
    1. Horning SJ,
    2. Chao NJ,
    3. Negrin RS,
    4. Hoppe RT,
    5. Long GD,
    6. Hu WW,
    7. et al.
    (1997) High-dose therapy and autologous hematopoietic progenitor cell transplantation for recurrent or refractory Hodgkin’s disease: analysis of the Stanford University results and prognostic indices. Blood 89:801–13.
    OpenUrlAbstract/FREE Full Text
    1. Josting A,
    2. Rueffer U,
    3. Franklin J,
    4. Sieber M,
    5. Diehl V,
    6. Engert A
    (2000) Prognostic factors and treatment outcome in primary progressive Hodgkin’s lymphoma: a report from the German Hodgkin Lymphoma Study Group. Blood 96:1280–6.
    OpenUrlAbstract/FREE Full Text
  15. ↵
    1. Yuen AR,
    2. Rosenberg SA,
    3. Hoppe RT,
    4. Halpern JD,
    5. Horning SJ
    (1997) Comparison between conventional salvage therapy and high-dose therapy with autografting for recurrent or refractory Hodgkin’s disease. Blood 89:814–22.
    OpenUrlAbstract/FREE Full Text
  16. ↵
    1. Pfreundschuh MG,
    2. Rueffer U,
    3. Lathan B,
    4. Schmitz N,
    5. Brosteanu O,
    6. Hasenclever D,
    7. et al.
    (1994) Dexa-BEAM in patients with Hodgkin’s disease refractory to multidrug chemotherapy regimens: a trial of the German Hodgkin’s Disease Study Group. J Clin Oncol 12:580–6.
    OpenUrlAbstract
    1. Josting A,
    2. Rudolph C,
    3. Reiser M,
    4. Mapara M,
    5. Sieber M,
    6. Kirchner HH,
    7. et al.
    (2002) Time-intensified dexamethasone/ cisplatin/cytarabine: an effective salvage therapy with low toxicity in patients with relapsed and refractory Hodgkin’s disease. Ann Oncol 13:1628–35.
    OpenUrlAbstract/FREE Full Text
    1. Moskowitz CH,
    2. Nimer SD,
    3. Zelenetz AD,
    4. Trippett T,
    5. Hedrick EE,
    6. Filippa DA,
    7. et al.
    (2001) A 2-step comprehensive high-dose chemoradiotherapy second-line program for relapsed and refractory Hodgkin disease: analysis by intent to treat and development of a prognostic model. Blood 97:616–23.
    OpenUrlAbstract/FREE Full Text
    1. Rodriguez J,
    2. Rodriguez MA,
    3. Fayad L,
    4. McLaughlin P,
    5. Swan F,
    6. Sarris A,
    7. et al.
    (1999) ASHAP: a regimen for cytoreduction of refractory or recurrent Hodgkin’s disease. Blood 93:3632–6.
    OpenUrlAbstract/FREE Full Text
    1. Colwill R,
    2. Crump M,
    3. Couture F,
    4. Danish R,
    5. Stewart AK,
    6. Sutton DM,
    7. et al.
    (1995) Mini-BEAM as salvage therapy for relapsed or refractory Hodgkin’s disease before intensive therapy and autologous bone marrow transplantation. J Clin Oncol 13:396–402.
    OpenUrlAbstract/FREE Full Text
    1. Martin A,
    2. Fernandez-Jimenez MC,
    3. Caballero MD,
    4. Canales MA,
    5. Perez-Simon JA,
    6. Garcia de Bustos J,
    7. et al.
    (2001) Long-term follow-up in patients treated with Mini-BEAM as salvage therapy for relapsed or refractory Hodgkin’s disease. Br J Haematol 113:161–71.
    OpenUrlCrossRefMedlineWeb of Science
    1. Baetz T,
    2. Belch A,
    3. Couban S,
    4. Imrie K,
    5. Yau J,
    6. Myers R,
    7. et al.
    (2003) Gemcitabine, dexamethasone and cisplatin is an active and non-toxic chemotherapy regimen in relapsed or refractory Hodgkin’s disease: a phase II study by the National Cancer Institute of Canada Clinical Trials Group. Ann Oncol 14:1762–7.
    OpenUrlAbstract/FREE Full Text
  23. ↵
    1. Kuruvilla J,
    2. Nagy T,
    3. Pintilie M,
    4. Tsang R,
    5. Keating A,
    6. Crump M
    (2006) Similar response rates and superior early progression-free survival with gemcitabine, dexamethasone, and cisplatin salvage therapy compared with carmustine, etoposide, cytarabine, and melphalan salvage therapy prior to autologous stem cell transplantation for recurrent or refractory Hodgkin lymphoma. Cancer 106:353–60.
    OpenUrlCrossRefMedlineWeb of Science
  24. ↵
    1. Bonfante V,
    2. Viviani S,
    3. Santoro A,
    4. Devizzi L,
    5. Di Russo A,
    6. Zanini M,
    7. et al.
    (1998) Ifosfamide and vinorelbine: an active regimen for patients with relapsed or refractory Hodgkin’s disease. Br J Haematol 103:533–7.
    OpenUrlCrossRefMedlineWeb of Science
  25. ↵
    1. Ferme C,
    2. Bastion Y,
    3. Lepage E,
    4. Berger F,
    5. Brice P,
    6. Morel P,
    7. et al.
    (1995) MINE regimen as intensive salvage chemotherapy for relapsed and refractory Hodgkin's disease. Ann Oncol 6:543–9.
    OpenUrlAbstract/FREE Full Text
  26. ↵
    1. Devizzi L,
    2. Santoro A,
    3. Bonfante V,
    4. Viviani S,
    5. Balzarini L,
    6. Valagussa P,
    7. et al.
    (1994) Vinorelbine: an active drug in the management of patients with heavily pre-treated Hodgkin’s disease. Ann Oncol 5:817–20.
    OpenUrlAbstract/FREE Full Text
  27. ↵
    1. Santoro A,
    2. Bredenfeld H,
    3. Devizzi L,
    4. Tesch H,
    5. Bonfante V,
    6. Viviani S,
    7. et al.
    (2000) Gemcitabine in the treatment of refractory Hodgkin’s disease: results of a multicenter phase II study. J Clin Oncol 18:2615–25.
    OpenUrlAbstract/FREE Full Text
  28. ↵
    1. Magagnoli M,
    2. Sarina B,
    3. Balzarotti M,
    4. Castagna L,
    5. Timofeeva I,
    6. Nozza A,
    7. et al.
    (2001) Mobilising potential of ifosfamide/vinorelbine-based chemotherapy in pretreated malignant lymphoma. Bone Marrow Transplant 28:923–7.
    OpenUrlCrossRefMedlineWeb of Science
  29. ↵
    1. Cheson BD,
    2. Horning SJ,
    3. Coiffier B,
    4. Shipp MA,
    5. Fisher RI,
    6. Connors JM,
    7. et al.
    (1999) Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas. NCI Sponsored International Working Group. J Clin Oncol 17:1244–54.
    OpenUrlAbstract/FREE Full Text
  30. ↵
    1. Smardova L,
    2. Engert A,
    3. Haverkamp H,
    4. Raemakers J,
    5. Baars J,
    6. Pfistner B,
    7. et al.
    (2005) Successful mobilization of peripheral blood stem cells with the DHAP regimen (dexamethasone, cytarabine, cisplatinum) plus granulocyte colony-stimulating factor in patients with relapsed Hodgkin's disease. Leuk Lymphoma 46:1017–22.
    OpenUrlCrossRefMedlineWeb of Science
    1. Akhtar S,
    2. Tbakhi A,
    3. Humaidan H,
    4. El Weshi A,
    5. Rahal M,
    6. Maghfoor I
    (2006) ESHAP + fixed dose G-CSF as auto logous peripheral blood stem cell mobilization regimen in patients with relapsed or refractory diffuse large cell and Hodgkin's lymphoma: a single institution result of 127 patients. Bone Marrow Transplant 37:277–82.
    OpenUrlCrossRefMedlineWeb of Science
  32. ↵
    1. McQuaker I,
    2. Haynes A,
    3. Stainer C,
    4. Byrne J,
    5. Russell N
    (1999) Mobilisation of peripheral blood stem cells with IVE and G-CSF improves CD34+ cell yields and engraftment in patients with non-Hodgkin's lymphomas and Hodgkin's disease. Bone Marrow Transplant 24:715–22.
    OpenUrlCrossRefMedlineWeb of Science
View Abstract
Back to top
Email
Print
Citation Tools
Request Permissions

Jump To

More in this TOC Section

Related Articles

Cited By...