Five Most Common Prognostically Important Fusion Oncogenes are Detected in the Majority of Pakistani Pediatric Acute Lymphoblastic Leukemia Patients and are Strongly Associated with Disease Biology and Treatment Outcome

Background and Objectives: Acute lymphoblastic leukemia (ALL) is a complex genetic disease involving many fusion oncogenes (FO) having prognostic significance. The frequency of various FO can vary in different ethnic groups, with important implications for prognosis, drug selection and treatment out...

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Published in:Asian Pacific journal of cancer prevention : APJCP Vol. 13; no. 11; pp. 5469 - 5475
Main Authors: Awan, Tashfeen, Iqbal, Zafar, Aleem, Aamer, Sabir, Noreen, Absar, Muhammad, Rasool, Mahmood, Tahir, Ammara H, Basit, Sulman, Khalid, Ahmad Mukhtar, Sabar, Muhammad Farooq, Asad, Sultan, Ali, Agha Shabbir, Mahmood, Amer, Akram, Muhammad, Saeed, Tariq, Saleem, Arsalan, Mohsin, Danish, Shah, Ijaz Hussain, Khalid, Muhammad, Asif, Muhammad, Haq, Riazul, Iqbal, Mudassar, Akhtar, Tanveer
Format: Journal Article
Language:Korean
Published: 2012
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Summary:Background and Objectives: Acute lymphoblastic leukemia (ALL) is a complex genetic disease involving many fusion oncogenes (FO) having prognostic significance. The frequency of various FO can vary in different ethnic groups, with important implications for prognosis, drug selection and treatment outcome. Method: We studied fusion oncogenes in 101 pediatric ALL patients using interphase FISH and RT-PCR, and their associations with clinical features and treatment outcome. Results: Five most common fusion genes i.e. BCR-ABL t (22; 9), TCF3-PBX1 (t 1; 19), ETV6-RUNX1 (t 12; 21), MLL-AF4 (t 4; 11) and SIL-TAL1 (del 1p32) were found in 89/101 (88.1%) patients. Frequency of BCR-ABL was 44.5% (45/101). BCR-ABL positive patients had a significantly lower survival ($43.7{\pm}4.24$ weeks) and higher white cell count as compared to others, except patients with MLL-AF4. The highest relapse-free survival was documented with ETV6-RUNX1 (14.2 months) followed closely by those cases in which no gene was detected (13.100). RFS with BCR-ABL, MLL-AF4, TCF3-PBX1 and SIL-TAL1 was less than 10 months (8.0, 3.6, 5.5 and 8.1 months, respectively). Conclusions: This is the first study from Pakistan correlating molecular markers with disease biology and treatment outcome in pediatric ALL. It revealed the highest reported frequency of BCR-ABL FO in pediatric ALL, associated with poor overall survival. Our data indicate an immediate need for incorporation of tyrosine kinase inhibitors in the treatment of BCR-ABL+ pediatric ALL in this population and the development of facilities for stem cell transplantation.
Bibliography:KISTI1.1003/JNL.JAKO201206735656289
ISSN:1513-7368
2476-762X