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844    Part VII  Hematologic Malignancies


          TABLE   Genetic Rearrangements in T-ALL
          56.18
         Transcription factor oncogenes
         Genetic Lesion                       Gene                 Frequency %                          Outcome
         t(1;14)(p32;q11)                     TAL1                 3                                    Poor/None
         t(1;7)(p32;q34)                      TAL1                 <1                                   Poor/None
         1p32 deletion                        TAL1                 25                                   Poor/None
         5’super-enhancer generating mutations  TAL1               5                                    Unknown
         t(7;9)(q34;q32)                      TAL2                 1                                    NA
         t(19)(q34;p13)                       LYL1                 1                                    NA
         t(14;21)(q11.2;q22)                  BHLHB1               1                                    NA
         t(11;14)(p15;q11)                    LMO1                 1                                    NA
         t(7;11)(q34;p15)                     LMO1                                                      NA
         t(11;14)(p13;q11)                    LMO2                 6                                    No impact
         t(7;11)(q34;p13)                     LMO2                 <1                                   No impact
         11p13 deletion                       LMO2                 3                                    No impact
         t(10;14)(q24;q11)                    TLX1                 5–10 Pediatric T-ALL                 No impact
         t(7;10(q35;q24)                      TLX1                 30 Adult T-ALL                       No impact
         del(10(q24-q26)                      TLX1                                                      No impact
         t(5;14)(q35;q32)                     TLX3                 20–25 Pediatric ALL and 5 Adult T-ALL  Unknown
         inv(7)(p15q34)                       HOXA                 3
         t(7;7)(p15q34)                       HOXA                 3
         t(10;11)(p13;q14)                    PICALM-MLL10         5–10                                 Poor
         t(11;19)(q23;p13)                    KMT2A-MLL1           5                                    Poor
         9q34 deletion                        SET-NUP214           3                                    Unknown
         inv(14)(q11.2q13)                    NKX2-1               5 Pediatric T-ALL                    Unknown
         inv(14)((q13q32.33)                  NKX2-1
         t(7;14)(q34;q13)                     NKX2-1
         t(14;20(q11;p11)                     NKX2-2               1                                    Unknown
         t(2;14)(q22;q32)                     ZEB2                 <1                                   NA
         t(6;7)(q23;q34)                      MYB                  3                                    NA
         t(8;14)(q24;q11)                     MYC                  1                                    NA
         NOTH1 pathway
         t(7;9)(q34;q34.3)                    NOTH1                <1                                   NA
         Activating mutations                 NOTH1                >60                                  good
         Activating mutations                 FBXW7                8–30                                 poor/none
         Cell Cycle
         9p21 deletion                        CDKN2A               >70                                  good
         t(7;12)(q34;p13)                     CCND2                3                                    NA
         13q14.2 deletion                     RB1                  12 Pediatric  T-ALL                  No impact
         12p13.2 deletion                     CDKN1B               12                                   NA
         Transcription factor tumor suppressors
         Inactivating mutation or deletion    WT1                  10                                   no imact
         Inactivating mutation or deletion    LEF1                 10–15                                NA
         Inactivating mutation or deletion    ETV6                 13                                   No impact
         Inactivating mutation or deletion    BCL11B               10                                   no imact
         Inactivating mutation or deletion    RUNX1                10–20                                no imact
         Inactivating mutation or deletion    GATA3                5                                    poor
         Signal transduction
         10q23 deletion                       PTEN                 10–15                                poor
         Inactivating mutation                PTEN                 10–15                                no imact
         Episomal 9q34 amplification          NUP214-ABL1          5                                    poor
         t(9;14)(q34;q32                      EML1-ABL1            <1                                   NA
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