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Augmented ICE in Patients With Poor-Risk Refractory and Relapsed Lymphomas
Sun Loo1, Andrew Lim1, Sze Ting Lee2
1Department of Clinical Haematology, Austin Health, Heidelberg, Victoria, Australia.
Dose-intensified ifosfamide and etoposide (augmented ICE) shows high response rates in relapsed/refractory lymphoma patients undergoing autologous stem cell transplant. This salvage chemotherapy regimen improves outcomes but increases toxicity.
Area of Science:
- Hematology
- Oncology
- Stem Cell Transplantation
Background:
- Salvage chemotherapy sensitivity is crucial for outcomes in relapsed/refractory lymphoma patients awaiting autologous stem cell transplant.
- Conventional dose ifosfamide, carboplatin, and etoposide (ICE) shows limited efficacy in patients with early relapse or primary refractory disease.
- Augmented ICE offers a dose-intensified approach to improve outcomes in this challenging patient population.
Purpose of the Study:
- To evaluate the response, deliverability, toxicities, and outcomes of augmented ICE in transplant-eligible patients with relapsed/refractory diffuse large-B-cell lymphoma (DLBCL) or Hodgkin lymphoma (HL).
Main Methods:
- Retrospective evaluation of 21 patients (13 DLBCL, 8 HL) receiving augmented ICE between 2010-2020.
- Augmented ICE involved higher doses of ifosfamide (10 g/m²) and etoposide (600 mg/m²) compared to standard ICE.
- Patients achieving complete or partial response proceeded to autologous stem cell transplant.
Main Results:
- High overall response rates: 85% for DLBCL and 100% for HL.
- 19 of 21 patients completed 2 cycles; 18 proceeded to transplant.
- Significant toxicities included febrile neutropenia (86%) and reversible ifosfamide encephalopathy (2 patients).
- 5-year OS/PFS: DLBCL (62%/45%), HL (100%/88%).
Conclusions:
- Augmented ICE demonstrates a high response rate and facilitates transplant realization in relapsed/refractory lymphoma.
- The intensified regimen comes at the cost of increased toxicity, requiring careful management.
- This approach offers a viable option for improving outcomes in select lymphoma patients.
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