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Outcome after HSCT in Philadelphia chromosome positive acute lymphoblastic leukemia in Sweden : a population-based study

Hulegardh, E. (author)
Dept Hematol & Coagulat, Sahlgrenska Univ Hosp, Gothenburg, Sweden,Sahlgrens University Hospital, Sweden
Hägglund, Hans (author)
Uppsala universitet,Karolinska Institutet,Hematologi
Ahlberg, Lucia (author)
Östergötlands Läns Landsting,Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet,Hematologiska kliniken US
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Karlsson, Karin (author)
Lund University,Lunds universitet,Stamcellscentrum (SCC),Avdelningen för stamcellsforskning,Institutionen för laboratoriemedicin,Medicinska fakulteten,Stem Cell Center,Division of stem cell research,Department of Laboratory Medicine,Faculty of Medicine,Skåne University Hospital, Sweden
Karbach, Holger (author)
Umeå universitet,Institutionen för strålningsvetenskaper
Markuszewska-Kuczynska, Alicja (author)
Umeå universitet,Institutionen för strålningsvetenskaper,Dept Hematol, Ctr Canc, Umeå Univ Hosp, Umeå, Sweden,Umeå University Hospital, Sweden
Persson, Inger (author)
Uppsala universitet,Statistiska institutionen
Åström, Maria, 1959- (author)
Region Örebro län,Department of Medicine, Hematology Section, Örebro University Hospital, Örebro, Sweden
Hallböök, Helene (author)
Uppsala universitet,Hematologi
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 (creator_code:org_t)
2014-06-26
2014
English.
In: Medical Oncology. - : Springer Science and Business Media LLC. - 1357-0560 .- 1559-131X. ; 31:8, s. 66-
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Even in the tyrosine kinase inhibitor era, allogeneic hematopoietic stem cell transplantation (HSCT) is regarded as standard care for adult Philadelphia (Ph) positive acute lymphoblastic leukemia (ALL). In this retrospective national study, we have reviewed the outcome after HSCT in Sweden for adult Ph-positive ALL between 2000 and 2009. In total, 51 patients with median age 42 (range 20-66) years underwent HSCT. Mainly allogeneic HSCT was performed (24 related donor, 24 unrelated donor and one cord blood), and only two patients were treated with an autologous HSCT. The 5-year OS was 51 (37-64) %. The probabilities of morphological relapse and non-relapse mortality (NRM) at 5 years were 36 (23-49) and 18 (9-29) %, respectively. For the allogeneic transplanted, the 5-year OS was for patients <40 years 70 (50-90) % and for patients >= 40 years 34 (16-52) %, p = 0.002. The 5-year probability of NRM was for patients <40 years 10 (2-28) % compared to 25 (11-42) % for patients >= 40 years (p = 0.04). Patients with chronic graft-versus-host disease (GVHD) had a 5-year morphological relapse probability of 20 (6-40) % compared to 59 (35-77) % for patients without chronic GVHD (p = 0.03). Age >= 40 years and the absence of chronic GVHD were confirmed as independent negative prognostic factors for relapse and non-relapse mortality in a multivariate analysis although the impact of chronic GVHD was significant only in the older age cohort.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

Acute lymphoblastic leukemia
Philadelphia chromosome
Graft-versus-host disease
Adult
Acute lymphoblastic leukemia
Philadelphia chromosome
Graft-versus-host
disease
Adult

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