SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:uu-380884"
 

Search: onr:"swepub:oai:DiVA.org:uu-380884" > Minimal residual di...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Minimal residual disease quantification by flow cytometry provides reliable risk stratification in T-cell acute lymphoblastic leukemia

Modvig, S (author)
Madsen, H O (author)
Umeå universitet,Patologi
Marincevic, Millaray, 1983- (author)
Uppsala universitet,Klinisk och experimentell patologi,Rose-Marie Amini
show more...
Rosthøj, S (author)
Tierens, A (author)
Juvonen, V (author)
Osnes, L T N (author)
Vålerhaugen, H (author)
Hultdin, M (author)
Thörn, Ingrid, 1957- (author)
Uppsala universitet,Klinisk och experimentell patologi,Rose-Marie Amini
Matuzeviciene, R (author)
Stoskus, M (author)
Marincevic, Millaray, 1983- (author)
Uppsala universitet,Klinisk och experimentell patologi,Rose-Marie Amini
Fogelstrand, L (author)
Lilleorg, A (author)
Toft, N (author)
Jónsson, O G (author)
Pruunsild, K (author)
Vaitkeviciene, G (author)
Vettenranta, K (author)
Lund, B (author)
Abrahamsson, J (author)
Schmiegelow, K (author)
Marquart, H V (author)
show less...
 (creator_code:org_t)
2018-12-14
2019
English.
In: Leukemia. - : Nature Publishing Group. - 0887-6924 .- 1476-5551. ; 33:6, s. 1324-1336
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Minimal residual disease (MRD) measured by PCR of clonal IgH/TCR rearrangements predicts relapse in T-cell acute lymphoblastic leukemia (T-ALL) and serves as risk stratification tool. Since 10% of patients have no suitable PCR-marker, we evaluated flowcytometry (FCM)-based MRD for risk stratification. We included 274 T-ALL patients treated in the NOPHO-ALL2008 protocol. MRD was measured by six-color FCM and real-time quantitative PCR. Day 29 PCR-MRD (cut-off 10-3) was used for risk stratification. At diagnosis, 93% had an FCM-marker for MRD monitoring, 84% a PCR-marker, and 99.3% (272/274) had a marker when combining the two. Adjusted for age and WBC, the hazard ratio for relapse was 3.55 (95% CI 1.4-9.0, p = 0.008) for day 29 FCM-MRD ≥ 10-3 and 5.6 (95% CI 2.0-16, p = 0.001) for PCR-MRD ≥ 10-3 compared with MRD < 10-3. Patients stratified to intermediate-risk therapy on day 29 with MRD 10-4-<10-3 had a 5-year event-free survival similar to intermediate-risk patients with MRD < 10-4 or undetectable, regardless of method for monitoring. Patients with day 15 FCM-MRD < 10-4 had a cumulative incidence of relapse of 2.3% (95% CI 0-6.8, n = 59). Thus, FCM-MRD allows early identification of patients eligible for reduced intensity therapy, but this needs further studies. In conclusion, FCM-MRD provides reliable risk prediction for T-ALL and can be used for stratification when no PCR-marker is available.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Klinisk laboratoriemedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Clinical Laboratory Medicine (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)

Keyword

Patologi
Pathology

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

  • Leukemia (Search for host publication in LIBRIS)

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view