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Interesting activity of pegylated liposomal doxorubicin in primary refractory and multirelapsed Hodgkin lymphoma patients: bridge to transplant
- Source :
- Hematological oncology. 36(2)
- Publication Year :
- 2017
-
Abstract
- Most patients with classical Hodgkin lymphoma (cHL) can be cured with frontline therapy, and those with relapsed or refractory (R/R) disease can often be cured with salvage therapy and autologous stem cell transplantation (ASCT).1-3 However, the prognosis of patients who relapse after or are ineligible to ASCT has historically been extremely poor, with a median overall survival of just over 2 years.1-3 Achieving durable responses in this patient population is a critical treatment goal so far only rarely achieved with conventional chemotherapy.4,5 Brentuximab vedotin (BV) has demonstrated efficacy in patients treated after failure of ASCT, with objective responses seen in 75% of patients in a phase 2 study.6 Recently, because of the unique genetics of cHL, the check point inhibitors nivolumab and pembrolizumab were tested in phase 1 to 2 studies that demonstrated objective responses in 70% to 85% heavily pretreated patients with R/R cHL.7-10 Among the different conventional salvage chemotherapy regimens and conventional single agents, such as bendamustine, BV, nivolumab, and pembrolizumab, there is another drug with interesting results in the setting of R/R cHL, but less known and used: the pegylated liposomal doxorubicin (PLD)
- Subjects :
- Oncology
Adult
Male
Cancer Research
medicine.medical_specialty
Pegylated Liposomal Doxorubicin
Polyethylene Glycols
03 medical and health sciences
0302 clinical medicine
Refractory
Recurrence
Internal medicine
medicine
Humans
Doxorubicin
Bridge to transplant
business.industry
Hematology
General Medicine
Middle Aged
Hodgkin Disease
030220 oncology & carcinogenesis
Hodgkin lymphoma
Female
business
030215 immunology
medicine.drug
Subjects
Details
- ISSN :
- 10991069
- Volume :
- 36
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Hematological oncology
- Accession number :
- edsair.doi.dedup.....a250ed5e537f13dbbc6950830cf9f8ba