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Table 3 Treatment exposure in patients treated to disease progression, adverse events in the absence of disease progression, and the overall treated population

From: Efficacy and safety profile of nab-paclitaxel plus gemcitabine in patients with metastatic pancreatic cancer treated to disease progression: a subanalysis from a phase 3 trial (MPACT)

Treatment exposure

Patients treated to PD

Patients treated to AEs

All treated patients

nab-P + Gem

(n = 224)

Gem

(n = 233)

nab-P + Gem

(n = 98)

Gem

(n = 58)

nab-P + Gem

(n = 421)

Gem

(n = 402)

Treatment duration, median, months

5.3

3.6

2.9

2.3

3.9

2.8

nab-P dose intensity, median, mg/m2/week

77.8

—

61.2

—

74.1

—

Gem dose intensity, median, mg/m2/week

626.3

695.9

523.4a

590.9

597.3

674.9

nab-P cumulative dose, median, mg/m2

1738

—

925

—

1425

—

Gem cumulative dose,

median, mg/m2

13,000

10,000

8000a

7500

11,400

9000

nab-P doses given at 125 mg/m2, %

72

—

62

—

71

—

Gem doses given at 1000 mg/m2, %

65

75

53

81

63

79

Patients with ≥ 1 nab-P dose reduction, n (%)

103 (46)

—

37 (38)

—

172 (41)

—

Patients with ≥ 1 Gem dose reduction, n (%)

114 (51)

89 (38)

48 (49)

19 (33)

198 (47)

132 (33)

Patients with ≥ 1 nab-P dose delay, n (%)

165 (74)

—

72 (73)

—

300 (71)

—

Patients with ≥ 1 Gem dose delay, n (%)

158 (71)

145 (62)

72 (73)

36 (62)

295 (70)

230 (57)

  1. AE adverse event, Gem gemcitabine, ITT intent-to-treat, nab-P nab-paclitaxel, PD progressive disease
  2. aBased on 97 evaluable patients