Table 2.

Characterization of Patients According to the Primary Tumor

CharacteristicsAdrenal N (%)AbdoP PGL N (%)HN PGL N (%)
N906316
Male66 (73)35 (56)6 (37)
Age at T0, y48,248,347,2
M1 <1 y39 (43)33 (52)7 (44)
Genetics
 N evaluable765916
 Sporadic52 (68)13 (21)4 (25)
 SDHB12 (13)42 (67)9 (56)
 SDHC / SDHD / MDH20 / 1 / 01 / 2 / 10 / 3 / 0
 VHL / MEN2 / NF14 / 3 / 400
Tumor-related syndrome41/87 (47)40 (63)13 (81)
Hormone-related syndrome53/87 (61)39 (62)4 (25)
Hypersecretiona71/80 (89)42/53 (79)3/12 (25)
Metastases
 Bone only14 (16)15 (24)6 (37)
 Soft tissue only49 (54)19 (30)5 (31)
CharacteristicsAdrenal N (%)AbdoP PGL N (%)HN PGL N (%)
N906316
Male66 (73)35 (56)6 (37)
Age at T0, y48,248,347,2
M1 <1 y39 (43)33 (52)7 (44)
Genetics
 N evaluable765916
 Sporadic52 (68)13 (21)4 (25)
 SDHB12 (13)42 (67)9 (56)
 SDHC / SDHD / MDH20 / 1 / 01 / 2 / 10 / 3 / 0
 VHL / MEN2 / NF14 / 3 / 400
Tumor-related syndrome41/87 (47)40 (63)13 (81)
Hormone-related syndrome53/87 (61)39 (62)4 (25)
Hypersecretiona71/80 (89)42/53 (79)3/12 (25)
Metastases
 Bone only14 (16)15 (24)6 (37)
 Soft tissue only49 (54)19 (30)5 (31)

Figures represent the number of evaluable patients (%), means ± SD, or median (IQR).

Abbreviations: AbdoP PGL, abdomino-pelvic paraganglioma; HN PGL, head and neck paraganglioma.

a

Hypersecreting tumor is defined as chromogranin A and/or metanephrines >2N.

Table 2.

Characterization of Patients According to the Primary Tumor

CharacteristicsAdrenal N (%)AbdoP PGL N (%)HN PGL N (%)
N906316
Male66 (73)35 (56)6 (37)
Age at T0, y48,248,347,2
M1 <1 y39 (43)33 (52)7 (44)
Genetics
 N evaluable765916
 Sporadic52 (68)13 (21)4 (25)
 SDHB12 (13)42 (67)9 (56)
 SDHC / SDHD / MDH20 / 1 / 01 / 2 / 10 / 3 / 0
 VHL / MEN2 / NF14 / 3 / 400
Tumor-related syndrome41/87 (47)40 (63)13 (81)
Hormone-related syndrome53/87 (61)39 (62)4 (25)
Hypersecretiona71/80 (89)42/53 (79)3/12 (25)
Metastases
 Bone only14 (16)15 (24)6 (37)
 Soft tissue only49 (54)19 (30)5 (31)
CharacteristicsAdrenal N (%)AbdoP PGL N (%)HN PGL N (%)
N906316
Male66 (73)35 (56)6 (37)
Age at T0, y48,248,347,2
M1 <1 y39 (43)33 (52)7 (44)
Genetics
 N evaluable765916
 Sporadic52 (68)13 (21)4 (25)
 SDHB12 (13)42 (67)9 (56)
 SDHC / SDHD / MDH20 / 1 / 01 / 2 / 10 / 3 / 0
 VHL / MEN2 / NF14 / 3 / 400
Tumor-related syndrome41/87 (47)40 (63)13 (81)
Hormone-related syndrome53/87 (61)39 (62)4 (25)
Hypersecretiona71/80 (89)42/53 (79)3/12 (25)
Metastases
 Bone only14 (16)15 (24)6 (37)
 Soft tissue only49 (54)19 (30)5 (31)

Figures represent the number of evaluable patients (%), means ± SD, or median (IQR).

Abbreviations: AbdoP PGL, abdomino-pelvic paraganglioma; HN PGL, head and neck paraganglioma.

a

Hypersecreting tumor is defined as chromogranin A and/or metanephrines >2N.

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