Skip to main content

Table 4 Phase II studies of gemcitabine/paclitaxel in patients with advanced or metastatic breast cancer

From: First-line therapy with gemcitabine and paclitaxel in locally, recurrent or metastatic breast cancer: A phase II study

Author

Regimen

No. of Pts

ORR % (CR %)

Median TTP (mos)

Comments

Vici et al26

G 1500 mg/m2 d1, 15 + T150 mg/m2 d1, 15 q4wks

20

45% (10%)

8

Heavily pretreated pts; supported with G-CSF

Colomer et al27

G 2500 mg/m2 d1 + T150 mg/m2 d1 q2wks

43

68% (21%)

9

Previously treated pts; hematologic toxicity

Delfino et al28

G 1200 mg/m2 d1, 8 + T 175 mg/m2 d1 q3wks

45

67% (22%)

11

Chemonaïve pts; mild hematologic toxicity; manageable toxicity

Sanchez-Rovira et al29

G 2500 mg/m2 d1, 15 + T 135 mg/m2 d1, 15 q4wks

44

45% (7%)

7

Previously treated pts; hematologic and neurologic toxicities

Murad et al30

G 1000 mg/m2 d1, 8 + T 175 mg/m2 d1 q3wks

29

55% (17%)

8

Heavily pretreated pts; 28-day reduced to a 21-day schedule due to hematologic toxicity

Genot et al (current study)

G 1200 mg/m2 d1, 8 T 175 mg/m2 d1 q3wks

40

40% (5.7%)

7.2

No prior treatment for metastatic disease, neutropenia prominent, other toxicities mild

  1. ORR = overall response rate; CR = complete response; TTP = time to progression; mos = months; G = gemcitabine; T = paclitaxel.