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. 2017 Sep 15;8(49):84729–84742. doi: 10.18632/oncotarget.20951

Table 2b. A list of patients who experienced recurrence of IDH mutant gliomas.

b. IDH mutant gliomas with TP53 mutation
Case Age, sex WHO Location Recurrent pattern sPFS (mo) OS (mo) F/U (mo)
TP53 mutation CNAs
M1-1 48F A Gr3 Lt frontal - 177 (alive) 183
R175H (exon 5) +1pter-34.2, +2q36-ter, +7, +9q34.1-ter, −13q14.3-21.3, +16pter-12, +19qcen-13.3, −21q
M1-2 63F GBM Lt frontal 1
+1p, +1q, −2q24.3-31, +2q33-ter, +3pter-23, −4q21.3-ter, +4qcen-13.1, +7, −9p, +9q21.2-21.3, −10q, −13q14.1-22, +17p13-cen, +17qcen-21.2, +18p11.2-cen, +18qcen-21.1, −18q22-ter, −19q, −21q,
M1-3 63F GBM Rt parietal 4
+1q, −2q24.3-32.1, +3p, +4qcen-13.1, −4q21.1-ter, +7, −9p, −11q, −13q14.2-22, −17q25-ter, −18q21.3-ter, −19q, −21q, −22q
M2-1 22F A Gr2 Rt insula - 72 (alive) 115
H193Y (exon 6) none
M2-2 28F A Gr3 Rt insula, temporal, frontal 2
−13q22, +18p, +19, −X
M3-1 46F A Gr2 Lt frontal - 26 (alive) 37
R306* (exon 8) +3p, −5p, +8 −11p, −13q12.1-21.3, +13q22-ter
M3-2 49F A Gr3 Lt frontal 1
+2p, −3q21-ter, +4pter-13.1, −4q21.1-ter, −7p, +7q, −8pter-23.1, −9p, −10q, −11p, −13qcen-22, +13q32-ter, −14q, −17q, −18q
M3-D 50F No OP Ventricular dissemnaiton 5
M4-1 34M A Gr3 Lt frontal NA 10 14 (dead)
IHC
M4-R 35M No OP Rt frontal 4
M5-1 44F A Gr2 Rt frontal - 27 65 (dead)
R273H (exon 8) −3p22-21, +7q, +8q22-ter, +11q23.3-ter, +12p, −13q21-31, −19q
M5-2 46F A Gr3 Rt frontal 1
−4q28-ter, +7q, +8q23-ter, +12p, −Xq
M5-R 47F No OP Lt frontal 4
M6-1 22F A Gr2 Lt frontal - 78 (alive) 108
R248W (exon 7) −11q22-23.1
M6-2 29F GBM Lt frontal 1
−3pter-3q24, −5p, +7, −11p, −11q22-23.1, −13q, −19q, −22, −X
M7-1 22M A Gr2 Rt frontal - 20 36 (dead)
IHC NA
M7-2 23M A Gr2 Rt frontal, Lt frontal 4
+7q, +8q, −19q
M8-1 33M A Gr2 Rt frontal - 12 (alive) 100
R273H (exon 8) +8q22.3-ter, −12q13-24.1
M8-2 34M A Gr3 Rt frontal 1
+4p, −4q, −5qcen-13, −5q21-ter, +8q13-ter, −9pter-21.3, −11p, +12p, −12q22-23
M8-3 38M HGG Rt cerebellum 4
−5q31.1-ter, +8q22.3-ter, +10p, −10q, +12p
M8-R 41M No OP midbrain 4
M8-R 42M No OP Bi basal nucleus 4
M9-1 61F A Gr2 Rt frontal - 20 (alive) 74
Y163C (exon 5) +7q31-ter, −X
M9-2 64F A Gr2 Rt frontal 1
+7q31.1-ter, +12q22-ter, −X
M10-1 30F A Gr2 Rt frontal - 41 (alive) 67
D281G (exon 8) −6q, −9p, −14q22-ter, −19q
M10-2 35F GBM Rt frontal 1
−3p, −6q, −9p. −12p, −14q, −15q, +18, −19q
M11-1 41M A Gr2 Lt frontal - 47 (alive) 78
R175H (exon 5) +7q, +10q24-ter
M11-2 45M A Gr2 Lt frontal 1
−5p, +7q, −18q21.1-ter
M11-3 47M A Gr3 Lt frontal 1
−5p, +7q, −8pter-23.1, −9p, −10pter-13, +10q26.1, −11p, −13qcen-22, −21q21, −22q, −X
M12-1 26M ND Rt frontal - 18 67 (dead)
Y236D (exon 7) +7q, +8q22.1-ter, +11q23.3-ter, +12p, +19
M12-2 30M GBM Rt frontal, lt frontal 4
−4q28-ter, +5pter-q23.3, +7q, +8q, −9p, −9q, −11pter-15.1, −11q23.1-ter, +12p, −13q21.1-22,
+13q31-ter
M12-3 31M HGG Rt frotanl , lt frontal 4
+7q, +8q, −9p, −X
M13-1 37F A Gr2 Lt insula - 29 102 (dead)
Y220C (exon 6) +7
M13-2 44F A Gr3 Lt insula, frontal 2
+2p, −3p21.3-11.2, +7, +8q23-ter, +10pter-12.3, −19q13.2-ter
M13-3 45F A Gr3 Rt frontal 4
NA
M14-1 30M A Gr2 Lt frontal - 9 (alive) 19
G287E (exon 8) +7q, −9p, +10p, +19p
M14-2 31M A Gr3 Lt frontal 1
NA
M14-R 32M No OP Rt frontal 3
M15-1 48M A Gr3 Lt frontal - 51 67 (dead)
R175H (exon5) −4q13-21, +7q, +13q31-ter, +X
M15-2 52M A Gr3 Lt frontal ∼ parietal 2
+2pter-22, +3pter-23, +4q21-24, +4q26-33, −6pter-22, −6q21-ter, +7q, −9pter-21, −12p13, +20q
M16-1 25M A Gr2 Lt parietal - 15 25 (dead)
IHC −4q22-ter, +5pter-23.3, −5q31.2-ter, +7, +8q, +13, −19q, −22
M16-2 27M GBM Lt Parietal 1
−3q11.2-24, +3q24.1-ter, +4p, −4q, +5pter-5q23.3, −5q31.2-ter, −6pter-22.1, +6p22.2-18.3, −6q21-26, +7, +8q, −9p, +13, −14q, +16q, +17q, −18, −19q, +21, −22
M16-RD 27M No OP Lt parietal, temporal, cerebellum 4

This table includes age at diagnosis, gender, histology, tumor location, radiological recurrence pattern, PFS, OS, follow-up time in months, location of the TP53 mutation (TP53 mutant tumors only), and CNAs obtained by metaphase CGH for 1p/19q co-deleted gliomas and TP53 mutant gliomas. The letters ‘R’ and ‘D’ indicate that remote recurrence and intraventricular dissemination were detected, respectively, although additional surgery was not performed. Abbreviation: CNA copy number aberration, PFS progression-free survival, OS overall survival, F/U follow-up, A diffuse or anaplastic astrocytoma, IDH-mutant, O (anaplastic) oligodendroglioma and 1p/19q-codeleted, IDH-mutant, HGG high-grade glioma, Gr grade, IHC immunohistochemistry