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Table 4 The RP occurrence in NSCLC patients treated with gemcitabine-based induction chemotherapy

From: Risk factors of grade ≥ 2 radiation pneumonitis after gemcitabine induction chemotherapy for patients with non-small cell lung cancer

Authors

Year

N

IC

Cycles of IC

RT dose (Gy)

CCRT

RP (Grade, %)

Ref

Guilbault C

2017

142

Gemcitabine+ Cisplatin

2

60

Gemcitabine+ Cisplatin

≥3, 10%

10

Kosmidis P

2007

43

Gemcitabine+Paclitaxel

2

63

Paclitaxel

≥2, 22%

21

Schallier D

2009

64

Gemcitabine+Carboplatin+ Paclitaxel

3

66

≥3, 12.5%

22

Blanco R

2008

56

Gemcitabine+Cisplatin

3

68.4

Gemcitabine

≥3, 34%

23

Belderbos J

2007

78

Gemcitabine+Cisplatin

2

66

≥3, 14%

24

Socinski MA

2008

26

Gemcitabine+Carboplatin

2

74

Gemcitabine

≥3, 37%

25

Arrieta O

2009

19

Gemcitabine+Carboplatin

2

60

Gemcitabine

≥3, 31.6%

26

Kocak M

2009

39

Gemcitabine+Cisplatin

3

66

Docetaxel+cisplatin

NR. 31%

27

Driesen P

2013

49

Gemcitabine+ Cisplatin

3

63

Gemcitabine+ Cisplatin

≥3, 6.5%

28

  1. IC Induction chemotheraoy, RT Radiotherapy, CCRT Concurrent chemoratiotherapy, RP Radiation pneumonitis, NR Not reffered, Ref Reference