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Allogeneic stem cell transplantation using lymphoablative rather than myeloablative conditioning regimen for relapsed or refractory lymphomas
Hematological oncology, 2017-03, Vol.35 (1), p.17-24
Yoon, Jae‐Ho
Jeon, Young‐Woo
Lee, Sung‐Eun
Cho, Byung‐Sik
Eom, Ki‐Seong
Kim, Yoo‐Jin
Lee, Seok
Kim, Hee‐Je
Min, Chang‐Ki
Lee, Jong‐Wook
Min, Woo‐Sung
Cho, Seok‐Goo
2017
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Yoon, Jae‐Ho
Jeon, Young‐Woo
Lee, Sung‐Eun
Cho, Byung‐Sik
Eom, Ki‐Seong
Kim, Yoo‐Jin
Lee, Seok
Kim, Hee‐Je
Min, Chang‐Ki
Lee, Jong‐Wook
Min, Woo‐Sung
Cho, Seok‐Goo
Titel
Allogeneic stem cell transplantation using lymphoablative rather than myeloablative conditioning regimen for relapsed or refractory lymphomas
Ist Teil von
Hematological oncology, 2017-03, Vol.35 (1), p.17-24
Ort / Verlag
England: Wiley Subscription Services, Inc
Erscheinungsjahr
2017
Quelle
Wiley-Blackwell Journals
Beschreibungen/Notizen
In relapsed or refractory non‐Hodgkin lymphoma (NHL), allogeneic hematopoietic stem cell transplantation (allo‐HSCT) provides graft‐versus‐lymphoma activity resulting in fewer incidences of relapse. However, therapy‐related mortality (TRM) remains an important challenge. We attempted to introduce our reduced‐intensity conditioning (RIC) regimen. From 2007 to 2013, we treated 28 relapsed or refractory NHLs with allo‐HSCT. All were pre‐conditioned with fludarabine [FLU, 180 mg/body surface area (BSA)/6 days] and melphalan (MEL, 70 mg/BSA/1 day); 25 (all but 3) were additionally treated with total body irradiation (TBI, 800 cGy/4Fx/2 days). Peripheral blood stem cells were collected from matched siblings (n = 10) or suitably matched unrelated (n = 18) donors. There were eight diffuse large B‐cell lymphomas, seven peripheral T‐cell lymphoma not otherwise specified, give lymphoblastic lymphomas, two mantle cell lymphomas, and six various other lymphomas. Of these patients, 10 relapsed after auto‐HSCT, 5 relapsed after chemotherapy, and 13 were refractory lymphomas. After allo‐HSCT, complete remission was achieved in 22 (78.5%) patients. After a median follow‐up of 24.8 months, 3‐year overall survival and disease‐free survival were 62.4 and 59.2% and the 3‐year TRM and relapse incidence were 14.9 and 28.6% respectively. Acute and chronic graft‐versus‐host diseases (GVHDs) were identified in 17 (≥Grade II in 12 patients) and 18 patients respectively, and the group with chronic GVHD showed favourable survival outcomes. In relapsed or refractory NHL, RIC‐allo‐HSCT using FLU + MEL + 800 cGy TBI showed favourable survival outcomes with acceptable TRM and relapse incidence. Copyright © 2015 John Wiley & Sons, Ltd.
Sprache
Englisch
Identifikatoren
ISSN: 0278-0232
eISSN: 1099-1069
DOI: 10.1002/hon.2201
Titel-ID: cdi_proquest_miscellaneous_1881769573
Format
–
Schlagworte
Adolescent
,
Adult
,
allogeneic
,
Antineoplastic Agents, Alkylating - administration & dosage
,
Disease-Free Survival
,
Female
,
Follow-Up Studies
,
Graft vs Tumor Effect
,
hematopoietic stem cell transplantation
,
Hematopoietic Stem Cell Transplantation - methods
,
Humans
,
Lymphoma
,
Lymphoma, Non-Hodgkin - therapy
,
Male
,
Melphalan - administration & dosage
,
Middle Aged
,
Myeloablative Agonists - administration & dosage
,
Neoplasm Recurrence, Local - therapy
,
non‐Hodgkin lymphoma
,
Prognosis
,
reduced intensity conditioning regimen
,
refractory
,
relapse
,
Retrospective Studies
,
Stem cells
,
Transplantation Conditioning - methods
,
Transplantation, Homologous - methods
,
Treatment Outcome
,
Vidarabine - administration & dosage
,
Vidarabine - analogs & derivatives
,
Whole-Body Irradiation
,
Young Adult
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