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Poster Discussion session - Haematological malignancies

2782 - ALK positive Anaplastic large cell lymphoma: molecular diagnosis and minimal residual disease monitoring

Date

21 Oct 2018

Session

Poster Discussion session - Haematological malignancies

Topics

Targeted Therapy

Tumour Site

Lymphomas

Presenters

Marketa Kalinova

Citation

Annals of Oncology (2018) 29 (suppl_8): viii359-viii371. 10.1093/annonc/mdy286

Authors

M. Kalinova1, L. Krskova2, M. Mrhalova3, E. Kabickova4, P. Riha4, R. Kodet2

Author affiliations

  • 1 Department Of Pathology And Molecular Medicine, 2nd Faculty of Medicine Motol University Hospital, 15006 - Prague /CZ
  • 2 Department Of Pathology And Molecular Medicine, 2nd Faculty of Medicine Motol University Hospital, 15006 - Prague/CZ
  • 3 Department Of Pathology And Molecular Medicine, Motol University Hospital, 15006 - Prague/CZ
  • 4 Department Of Paediatric Haematology And Oncology, 2nd Faculty of Medicine Motol University Hospital, 15006 - Prague/CZ
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Resources

Abstract 2782

Background

ALK positive anaplastic large cell lymphoma (ALCL) is characterized by expression of the anaplastic lymphoma kinase (ALK), frequently associated with the t(2;5)(p23;q35), fusing the ALK and nucleophosmin (NPM) genes. In the remaining cases immunohistochemically (IHC) proven ALK+ ALCL, the ALK gene was shown to have various translocation partners.

Methods

In our study molecular diagnostics included detection of the most frequent fusion gene NPM/ALK by PCR. NPM/ALK negative tumors were analyzed by ALK specific Rapid Amplification of 5´cDNA Ends (5´ RACE). Molecular findings were correlated with IHC localization of ALK protein, I-FISH and with expression of the 3´end of ALK mRNA using quantitative PCR (Q-RT-PCR). We monitored minimal residual disease (MRD) using Q-RT-PCR of the 3´end of ALK mRNA. 5´RACE is a method for detection of unknown translocation partners of a fusion gene. We prepared Q-RT-PCR assay for the quantitative assessment of quantification of 3´end ALK mRNA, and housekeeping gene.

Results

We analysed ALK+ ALCL from 76 patients (1-80 years, median 17 years). Chromosomal breakpoints affecting the ALK locus were detected by I-FISH in all investigated tumors. The NPM/ALK was detected in 57/76 patients. 5´RACE identified ATIC/ALK in 7 patients, CLTC/ALK in 2 patients. Other fusion genes (TPM4/ALK, TPM3/ALK, ALO17/ALK, MYH9/ALK) were each found separately in single individual patients. In all specimens, overexpression of 3´end ALK mRNA suitable for the MRD detection was found (median 69462 copies). We evaluated MRD by the monitoring 3´end of ALK mRNA levels in 430 residual samples (149x bone marrow, 269x peripheral blood) from 31 ALK+ ALCL patients with median follow-up time 798 days. Levels of 3´end ALK mRNA showed a good correlation with clinical course of the disease.

Conclusions

Molecular diagnostics allows for detecting translocation partners of ALK gene. Q-RT-PCR based analysis of 3´end ALK mRNA is a promising and rapid approach for diagnostics and MRD monitoring of patients with ALK+ ALCL.

Clinical trial identification

Legal entity responsible for the study

Ministry of Health, Czech Republic.

Funding

Supported by the project (Ministry of Health, Czech Republic) for conceptual development of research organization 00064203 (University Hospital Motol, Prague, Czech Republic).

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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