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Table 1 Summary of clinical and tumor attributes

From: Longitudinal multi-omics study of palbociclib resistance in HR-positive/HER2-negative metastatic breast cancer

 

Number

Median

Range

Number of patients

71

  

Age, years (median, range)

71

45

31–71

Menopausal status

70

  

 Premenopause

41 (59%)

  

 Postmenopause

29 (41%)

  

Pathologic subtype

71

  

 IDC

67 (94%)

  

 ILC

2 (3%)

  

 Etc. and unknown

2 (3%)

  

Breast cancer family history

53

  

 Yes

6 (11%)

  

 No

47 (89%)

  

BRCA1/2 pathogenic mutationa

64

  

 Wild-type

56 (88%)

  

 Mutated

8 (12%)

  

Endocrine therapy

71

  

 Letrozole

48 (68%)

  

 Letrozole + GnRH agonist

2 (3%)

  

 Exemestane + GnRH agonist

14 (20%)

  

 Fulvestrant

7 (10%)

  

Progressive disease event

51 (72%)

  

PFS, months

71

15

95% CI (8.6, 20.4)

 < 6

20 (28%)

  

 6–20

32 (45%)

  

 ≥ 20

19 (27%)

  

Metastasis

71

  

 De novo

32 (45%)

  

 Relapsed

39 (55%)

  

RECIST tumor response

71

  

 Complete response

3 (4%)

  

 Partial response

29 (41%)

  

 Stable disease

27 (38%)

  

 Progressive disease

12 (17%)

  

Palliative line of palbociclib

71

  

 First line

55 (77%)

  

 Second and later lines

16 (23%)

  

Follow-up from palbociclib treatment (months)

71

20

3–48

  1. IDC invasive ductal carcinoma, ILC invasive lobular carcinoma, GnRH gonadotropin-releasing hormone, PFS progression-free survival, RECIST Response Evaluation Criteria in Solid Tumors
  2. aBRCA1/2 pathogenic mutation was determined considering both germline and somatic mutations that truncate protein reading frame or annotated as pathogenic in ClinVar. Different types of endocrine therapies were combined with palbociclib. The median PFS of our cohort was 15 months, and the median follow-up duration was 20 months