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. 2021 Sep 14;13(18):4603. doi: 10.3390/cancers13184603

Table 1.

Overview of the studies with and without bevacizumab in ovarian cancer.

Study Name
Author, Year [Ref]
Study Population,
Number
Regimen mPFS (Months)
p Value
mOS (Months)
p Value
VTE
n/N (%)
ATE
n/N (%)
GOG-0218
Tewari, 2018 [16]
Frontline stage III
(incomplete resection)
and stage IV (all)
N = 1873
A: C + P + pbo x6
B: C + P + bev x6
C: C + P + bev x6
→ bev x16
A: 10.3 m
B: 11.3 m
C: 14.1 m
A: 41.1 m
B: 40.8 m
C: 43.3 m
A: 35/601 (5.8%)
B: 36/607 (5.9%)
C: 42/608 (6.9%)
A: 5/601 (0.7%)
B: 4/607 (0.7%)
C: 4/608 (0.7%)
ICON-7
Perren, 2011 [17]
Frontline
stage I-IIa (high risk)
OR stage IIb-IV
N = 1498
A: C + P + pbo x6
→ pbo x10
B: C + P + bev1 x6
→ bev1 x10
A: 17.5 m
B: 19.9 m
A: 58.6 m
B: 58.0 m
A: 31/753 (4.1%)
B: 50/745 (6.7%)
A: 11/753 (1.4%)
B: 27/745 (3.6%)
ANTHALYA
Joly, 2017 [33]
Frontline stage IIIc-IV neoadjuvant
N = 99
A: C + P x4 → IDS
→ C + P + bev x1
→ bev x16
B:(C + P) x4 + bev x3
→IDS
→(C + P) x2 + bev x1
→ bev x16
A: 21.2 m [14.5–26.7]
B: 23.5 m [18.5–30.6]
NA A: 2/37 (5%)
B: 6/58 (11%)
NA
GEICO-1205
Garcia-Garcia,
2019 [34]
Frontline FIGO IIIc-IV OC neoadjuvant
N = 68
A: C + P x4 → IDS
→C + P + bev x3
→ bev x15
B: C + P + bev x4
→ IDS
→ C + P + bev x3
→ bev x15
A: 20.1 m
B: 20.4 m
NA A: 0/33 (0%) *
B: 2/35 (5.7%) *
NA
mEOC/GOG0421
Gore, 2019 [35]
Frontline mucinous
stage II-IV
or relapsed stage I
N = 50
A: C + P x6 vs.
B: Ox + Cap x6 vs.
C: C + P + Bev x6
→ bev x12 vs.
D: Ox + Cap + Bev x6
→ bev x12
A&B: 8.1 m
C&D: 18.1 m
A&B: 32.7 m
C&D: 27.7 m
A&B: 0/26 (0%) *
C&D:1/24 (4.1%) *
NA
Zhang, 2020 [36] Frontline stage I-III
N = 100
A: C
B: Npl85 + bev1
A: NA
B: NA
A: NA
B: NA
A: NA
B: NA
A: NA
B: NA
OCEANS
Aghajanian, 2015 [20]
Relapsed
platinum-sensitive
N = 484
A: C + G + pbo x6
B: C + G + bev x6
→ bev maintenance
A: 8.4 m
B: 12.4 m
A: 32.9 m
B: 33.6 m
A: 6/233 (2.6%) *
B:11/247 (4.5%) *
A: 1/233 (0.4%)
B: 6/247 (2.4%)
GOG-0213
Coleman, 2017
[21]
Relapsed
platinum-sensitive
N = 674
A: C + P
B: C + P + bev x6
→ bev maintenance ***
A: 10.4 m
B: 13.8 m
A: 37.3 m
B: 42.2 m
A: 0/327 (0%)
B: 0/330 (0%)
A: 6/327 (1.8%)
B: 22/330 (6.6%)
MITO16B-MaNGO OV2B-ENGOT OV17
Pignata, 2021 [37]
Relapsed
platinum sensitive,
prior bevacizumab
N = 406
A: C + P or C + G
or C + PLD
B: C + P or C + G
or C + PLD + bev2
A: 8.8 m
B: 11.8 m
A: 27.1 m
B: 26.7 m
NA ** NA **
NSGO-AVANOVA2/
ENGOT-OV24
Mirza, 2019 [38]
Relapsed
platinum sensitive
N = 97
A: niraparib
B: niraparib + bev
A: 5.5 m
B: 11.9 m
NA A: 1/48 (2.2%)
B: 2/49 (4.2%)
NA
Cong, 2019 [39] Relapsed
platinum sensitive
N = 164
A: C + P
B: C + P + bev2
A: 6.7 m
B: 9.3 m
A: 12.5 m
B: 18.5 m
NA NA
AURELIA
Pujade-Lauraine, 2014 [22]
Relapsed
platinum resistant
N = 360
A: wP or Tp or PLD
B: wP or Tp or PLD + bev
A: 3.4 m
B: 6.7 m
A: 13.3 m
B: 16.6 m
A: 8/181 (4.4%) *
B: 5/179 (2.8%) *
A: 0/181 (0%)
B: 4/179 (2.2%)
Liu, 2019 [41] Relapsed
platinum resistant
N = 86
A: ABP
B: ABP + bev1
A: 6.7 m
B: 8.9 m
A: 12.7 m
B: 16.3 m
NA NA
Zhang, 2019 [40] Relapsed
platinum sensitive
N = 160
A: DTx + Npl80
B: DTx + Npl80 + bev1
A: 8.6 m
B: 12.2 m
A: 17.7 m
B: 22.5 m
NA NA

ABP: albumin-bound paclitaxel 135–175 mg/m2 Q3w x6; ATE: arterial thromboembolic events; bev = bevacizumab 15 mg/kg IV Q3w; bev1 = bevacizumab 7.5 mg/kg IV Q3w; bev2 = bevacizumab 10 mg/kg IV Q2w or 15 mg/kg Q3w; C: carboplatin 400 mg/m2 Q3w x3; C + G: Carboplatin AUC4 Q3w + gemcitabin 1250 mg/m2 d1 + 8; C + P: carboplatin AUC5-6 Q3w + paclitaxel 175 mg/m2 Q3w x6; C + PLD: carboplatin AUC5 + pegylated liposomal doxorubicin 30 mg/m2 Q4w; DTX: Docetaxel 75 mg/m2; PLD: pegylated liposomal doxorubicin 40 mg/m2 Q4w; IDS: interval debulking surgery; mPFS: median progression-free survival expressed in months; mOS: median overall survival expressed in months; NA: not available; Npl80: nedaplatin 80 mg/m2 Q3w; Npl85: nedaplatin 85 mg/m2 Q3w x6; niraparib: 300 mg once daily; Ox-Cap: oxaliplatin 130 mg/m2 intravenous d1 Q2w + capecitabine 850 mg/m2 orally bid d1–14; pbo: placebo; Tp: Topotecan 4 mg/m2 d1–8–15 Q3w; VTE: venous thromboembolism (all grades unless otherwise specified); wP: Paclitaxel 80 mg/m2 d1–8–15–22 Q4w. * Grade ≥ 3 VTE. ** all thromboembolic events: 5/200 (A) vs. 6/200 (B) *** 2 × 2 design: surgery vs. no surgery; bevacizumab vs. no bevacizumab. Data shown with/without bevacizumab. Surgery analysis was done in a separate publication.