Poor prognosis for P2RY8-CRLF2 fusion but not for CRLF2 over-expression in children with intermediate risk B-cell precursor acute lymphoblastic leukemia
Pediatric B-cell precursor acute lymphoblastic leukemia (BCP-ALL) has achieved an 80% cure rate as a result of a risk-adapted therapy largely based on minimal residual disease (MRD) monitoring. However, relapse is still the most frequent adverse event, occurring mainly in the patients with intermedi...
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Veröffentlicht in: | Leukemia 2012-10, Vol.26 (10), p.2245-2253 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Pediatric B-cell precursor acute lymphoblastic leukemia (BCP-ALL) has achieved an 80% cure rate as a result of a risk-adapted therapy largely based on minimal residual disease (MRD) monitoring. However, relapse is still the most frequent adverse event, occurring mainly in the patients with intermediate MRD levels (intermediate risk, IR), emphasizing the need for new prognostic markers. We analyzed the prognostic impact of cytokine receptor-like factor 2 (
CRLF2
) over-expression and
P2RY8-CRLF2
fusion in 464 BCP-ALL patients (not affected by Down syndrome and
BCR-ABL
negative) enrolled in the AIEOP-BFM ALL2000 study in Italy. In 22/464 (4.7%) samples, RQ-PCR showed
CRLF2
over-expression (⩾20 times higher than the overall median).
P2RY8-CRLF2
fusion was detected in 22/365 (6%) cases, with 10/22 cases also showing
CRLF2
over-expression.
P2RY8-CRLF2
fusion was the most relevant prognostic factor independent of
CRLF2
over-expression with a threefold increase in risk of relapse. Significantly, the cumulative incidence of relapse of the
P2RY8-CRLF2+
patients in the IR group was high (61.1%±12.9 vs 17.6%±2.6,
P |
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ISSN: | 0887-6924 1476-5551 |
DOI: | 10.1038/leu.2012.101 |