Tags

Type your tag names separated by a space and hit enter

Clinical impact of nucleophosmin mutations and Flt3 internal tandem duplications in patients older than 60 yr with acute myeloid leukaemia.
Eur J Haematol. 2008 Mar; 80(3):208-15.EJ

Abstract

BACKGROUND

Nucleophosmin (NPM1) and Flt3 internal tandem duplications (Flt3-ITD mutations) represent the most frequent molecular aberrations in patients with acute myeloid leukemia (AML). While NPM1 mutations are associated with favourable prognosis in younger AML patients, Flt3-ITD mutations reflect an unfavourable prognostic factor in these patients. So far, especially NPM1 mutations have not yet been evaluated exclusively in older patients.

PATIENTS AND METHODS

We retrospectively analysed the prevalence of NPM1 and Flt3-ITD mutations and its association with complete remission (CR), and survival in 99 elderly patients (median age 71 yr, range 60-85 yr) newly diagnosed for AML. Primary treatment approach was curative in 54, and palliative in 38 patients, while seven patients received best supportive care only. The mean follow-up of surviving patients was 600 d.

RESULTS

Sixty-seven patients were tested negative for NPM1 and Flt3-ITD mutations (group 1), 16 patients carried only a NPM1 mutation (group 2) and nine patients had only a Flt3-ITD mutation (group 3) while additional seven patients were positive for both aberrations (group 4). We can demonstrate a significant higher rate of CR comparing wildtype vs. NPM1 positive patients (40.5% for group 1 vs. 80.0% for group 2, P = 0.03) for patients receiving curative therapy. Interestingly, there is no significant difference in overall survival between group 1 and group 2 (Log-rank test P = 0.22, median 440 d vs. 1125 d). In contrast, patients carrying a Flt3-ITD mutation had a significant worse overall survival compared to wildtype patients (P = 0.03, median 210 d for group 3 + 4 vs. 634 d for group 1 + 2) while no difference of CR rate could be observed (42.8% vs. 48.9%, P = 0.91).

CONCLUSION

As elderly but medically fit patients with AML carrying a NPM1 mutation have a high CR rate, age itself should not be a barrier for induction treatment. However, new therapeutic concepts of postremission therapy (e.g. allogeneic stem cell transplantation after dose-reduced conditioning) should be considered for these patients in first CR.

Authors+Show Affiliations

Department of Internal Medicine II (Oncology and Hematology), Universitätsklinikum, Jena, Germany. sebastian.scholl@med.uni-jena.deNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

18081718

Citation

Scholl, Sebastian, et al. "Clinical Impact of Nucleophosmin Mutations and Flt3 Internal Tandem Duplications in Patients Older Than 60 Yr With Acute Myeloid Leukaemia." European Journal of Haematology, vol. 80, no. 3, 2008, pp. 208-15.
Scholl S, Theuer C, Scheble V, et al. Clinical impact of nucleophosmin mutations and Flt3 internal tandem duplications in patients older than 60 yr with acute myeloid leukaemia. Eur J Haematol. 2008;80(3):208-15.
Scholl, S., Theuer, C., Scheble, V., Kunert, C., Heller, A., Mügge, L. O., Fricke, H. J., Höffken, K., & Wedding, U. (2008). Clinical impact of nucleophosmin mutations and Flt3 internal tandem duplications in patients older than 60 yr with acute myeloid leukaemia. European Journal of Haematology, 80(3), 208-15.
Scholl S, et al. Clinical Impact of Nucleophosmin Mutations and Flt3 Internal Tandem Duplications in Patients Older Than 60 Yr With Acute Myeloid Leukaemia. Eur J Haematol. 2008;80(3):208-15. PubMed PMID: 18081718.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Clinical impact of nucleophosmin mutations and Flt3 internal tandem duplications in patients older than 60 yr with acute myeloid leukaemia. AU - Scholl,Sebastian, AU - Theuer,Claudia, AU - Scheble,Veit, AU - Kunert,Christa, AU - Heller,Anita, AU - Mügge,Lars-Olof, AU - Fricke,Hans-Joerg, AU - Höffken,Klaus, AU - Wedding,Ulrich, PY - 2007/12/18/pubmed PY - 2008/3/4/medline PY - 2007/12/18/entrez SP - 208 EP - 15 JF - European journal of haematology JO - Eur J Haematol VL - 80 IS - 3 N2 - BACKGROUND: Nucleophosmin (NPM1) and Flt3 internal tandem duplications (Flt3-ITD mutations) represent the most frequent molecular aberrations in patients with acute myeloid leukemia (AML). While NPM1 mutations are associated with favourable prognosis in younger AML patients, Flt3-ITD mutations reflect an unfavourable prognostic factor in these patients. So far, especially NPM1 mutations have not yet been evaluated exclusively in older patients. PATIENTS AND METHODS: We retrospectively analysed the prevalence of NPM1 and Flt3-ITD mutations and its association with complete remission (CR), and survival in 99 elderly patients (median age 71 yr, range 60-85 yr) newly diagnosed for AML. Primary treatment approach was curative in 54, and palliative in 38 patients, while seven patients received best supportive care only. The mean follow-up of surviving patients was 600 d. RESULTS: Sixty-seven patients were tested negative for NPM1 and Flt3-ITD mutations (group 1), 16 patients carried only a NPM1 mutation (group 2) and nine patients had only a Flt3-ITD mutation (group 3) while additional seven patients were positive for both aberrations (group 4). We can demonstrate a significant higher rate of CR comparing wildtype vs. NPM1 positive patients (40.5% for group 1 vs. 80.0% for group 2, P = 0.03) for patients receiving curative therapy. Interestingly, there is no significant difference in overall survival between group 1 and group 2 (Log-rank test P = 0.22, median 440 d vs. 1125 d). In contrast, patients carrying a Flt3-ITD mutation had a significant worse overall survival compared to wildtype patients (P = 0.03, median 210 d for group 3 + 4 vs. 634 d for group 1 + 2) while no difference of CR rate could be observed (42.8% vs. 48.9%, P = 0.91). CONCLUSION: As elderly but medically fit patients with AML carrying a NPM1 mutation have a high CR rate, age itself should not be a barrier for induction treatment. However, new therapeutic concepts of postremission therapy (e.g. allogeneic stem cell transplantation after dose-reduced conditioning) should be considered for these patients in first CR. SN - 1600-0609 UR - https://www.unboundmedicine.com/medline/citation/18081718/Clinical_impact_of_nucleophosmin_mutations_and_Flt3_internal_tandem_duplications_in_patients_older_than_60_yr_with_acute_myeloid_leukaemia_ L2 - https://doi.org/10.1111/j.1600-0609.2007.01019.x DB - PRIME DP - Unbound Medicine ER -