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3.

Selected phase III trials addressing the role of chemotherapy in stage IVB, recurrent or persistent CC

Author (ref.) No. of patients Histology Reference regimen Regimen investigated Survival (months)
CC, cervical cancer; SCC, squamous cell carcinoma; ADC, adenocarcinoma; ADS, adenosquamous carcinoma; CDDP, cisplatin; PTX, paclitaxel; TOP, topotecan; 1, MVAC arm (Methotrexate 30 mg/m2 d 1, 15, 22 + vinblastine 3 mg/m2 d 2, 15, 22 + doxorubicin 30 mg/m2 d 2 + cisplatin 70 mg/m2 d 2, q 21 d) closed prematurely due to severe adverse effect; GEM, gemcitabine; VNR, vinorelbine; Bev, bevacizumab; CBDCA, carboplatin; PFS, progression-free survival; OS, overall survival; NS, not significant.
Moore et al.
(2004) (53)
169 SCC CDDP 50 mg/m2
q 21 d
CDDP 50 mg/m2 +
PTX 135 mg/m2/24 h
q 21 d
PFS 2.8 vs. 4.8
(P<0.01)
Long et al.
(2005) (54)
179 SCC,
ADC,
ADS
CDDP 50 mg/m2
q 21 d
CDDP 50 mg/m2 +
TOP 0.75 mg/m2
d 1–3, q 21 d
MVAC1
PFS 2.9 vs. 4.6
(P<0.01)
Monk et al.
(2009) (55)
204 SCC,
ADC,
ADS
CDDP 50 mg/m2 +
PTX 135 mg/m2/24 h
q 21 d
CDDP 50 mg/m2 +
TOP 0.75 mg/m2
d 1–3, q 21 d
CDDP 50 mg/m2 +
GEM 1,000 mg/m2
d 1, 8
CDDP 50 mg/m2 +
VNR 30 mg/m2
PFS 5.8 vs. 4.6 vs. 4.7
vs. 4.0 (NS)
Tewari et al.
(2014) (56,57)
452 SCC,
ADC,
ADS
CDDP 50 mg/m2 +
PTX 135 mg/m2/24 h
or 175 mg/2 3 h, q 3 w,
or TOP 0.75 mg/m2
d 1–3 + PTX
175 mg/m2/3 h,
d 1 q 3 w
CDDP 50 mg/m2 +
PTX 135 or 175 mg/m2
+ Bev 15 mg/kg q 3 w,
or TOP 0.75 mg/m2 d 1–3 +
PTX 175 mg/m2, d 1 +
Bev 15 mg/kg q 3 w
OS 16.8 Bev + vs.
13.3 Bev– (P=0.007)
Kitagawa et al.
(2015) (58)
244 SCC,
ADC,
ADS
CDDP 50 mg/m2 +
PTX 135 mg/m2/24 h,
q 3 w
CBDCA (AUC 5) +
PTX 175 mg/m2/3 h
q 3 w
PFS 18.3 vs. 17.5
(NS)