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Clinical Significance of ALK-1 Gene Abnormalities in Diffuse Large Cell Lymphoma
- Source :
- Clinical Medicine Insights. Oncology, Clinical Medicine Insights: Oncology, Vol 6 (2012), Clinical Medicine Insights: Oncology, Vol 2012, Iss 6, Pp 395-405 (2012)
- Publication Year :
- 2012
-
Abstract
- Objectives To detect relative frequency of anaplastic lymphoma kinase (ALK-1) gene abnormality in diffuse large cell lymphoma (DLCL) using fluorescence in situ hybridization (FISH), and correlate its presence with clinicopathological features which may be useful for choice of therapy and predict survival in newly diagnosed cases. Patients and Methods A prospective study was done between March 2004 and October 2009. Fifty patients newly diagnosed with DLCL were enrolled into the study. Immunophenotyping was done and detection of ALK-1 gene abnormalities were carried out by immunohistochemically (IHC) and FISH. Patients that proved to be ALK-1 positive were treated with standard cyclophosphamide –hydroxydaunorubicin-oncovin-prednisone (CHOP) protocol. Results All ALK +ve patients achieved complete remission (CR) vs. 93.5% CR and 6.5% partial remission (PR) for ALK –ve patients respectively. Disease free survival (DFS) at 24 months was 81.8% in the CHOP-14 group (ALK-1−) vs. 100% for the CHOP-21 group (ALK-1+). Overall survival (OS) at 30 months was 80.4% in the CHOP-14 group vs. 100% for the CHOP-21 group.
- Subjects :
- medicine.medical_specialty
Cyclophosphamide
CHOP
Bioinformatics
Gastroenterology
lcsh:RC254-282
Immunophenotyping
FISH
Internal medicine
hemic and lymphatic diseases
medicine
Anaplastic lymphoma kinase
Clinical significance
Prospective cohort study
ALK-1
Original Research
medicine.diagnostic_test
business.industry
Cancer
medicine.disease
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
ALCL
Oncology
business
Fluorescence in situ hybridization
medicine.drug
IHC
Subjects
Details
- ISSN :
- 11795549
- Volume :
- 6
- Database :
- OpenAIRE
- Journal :
- Clinical Medicine Insights. Oncology
- Accession number :
- edsair.doi.dedup.....d408b435d0e573ec1f92c700ae27548a