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. Author manuscript; available in PMC: 2022 Mar 1.
Published in final edited form as: Gynecol Oncol. 2020 Dec 26;160(3):786–792. doi: 10.1016/j.ygyno.2020.12.007

Table 2:

Cohort demographics

N (total 393) %

Mean age at diagnosis (SD) 59.9 (12.4)

Histology:
  High grade serous 281 71.5%
  Low grade serous 21 5.3%
  Endometrioid 28 7.1%
  Clear cell 21 5.3%
  Adenocarcinoma 19 4.8%
  Carcinosarcoma 14 3.6%
  Other 9 2.3%

Grade:
  1-2 35 8.9%
  3 355 90.3%
  Unknown 3 0.8%

Stage*:
  I 34 8.7%
  II 23 5.9%
  III 275 70.0%
  IV 55 14.0%
  Unknown 6 1.5%

Platinum Response:
  Sensitive 219 68.2%
  Resistant/refractory 82 31.8%
  Unknown 92 55.7%

Cytoreduction:
  Optimal 274 69.7%
  Suboptimal 106 27.0%
  Unknown 13 3.3%

Neoadjuvant chemotherapy:
  Yes 48 12.2%
  No 332 84.5%
  Unknown 13 3.3%

BRCA1 or BRCA2§:
  Wildtype 302 76.8%
  Germline mutation 65 16.5%
  Somatic mutation 27 6.9%

Other HRD genes|:
  Wildtype 372 94.7%
  Germline or somatic mutation 21 5.3%

TP53:
  Wildtype 91 23.2%
  Germline or somatic mutation 302 76.8%
*

Staged according to 1988 International Federation of Gynecology and Obstetrics (FIGO) ovarian cancer staging classification.

Platinum sensitive: no recurrence or progression within 6 months of platinum-containing primary adjuvant treatment.

Optimal: less than 1 cm of residual disease.

§

One case with both somatic and germline mutation included in both categories.

|

HRD mutations (excluding BRCA1 or BRCA2) include ATM, BARD1, BRIP1, NBN, PALB2, RAD51C, and RAD51D.