Table 1.
Study | Country | Study Design | Treatment Period | No.of Patient | Male, % | Mean Age (y) | Initial ICI |
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Regimen(i) | Therapy Line | TPS ≥ 50% (%)a | PFSi (M) | Best Response |
G3/4 IrAE | Cessation Reason | |||||||||||
CR | PR | Stable Disease | PD | NR | |||||||||||||
Bernard et al., 201813 | France | Retrospective | 2012.5–2017.10 | 1 | NR | NR | Anti–PD-(L)1 | NR | NR | 19.9 | 0 | 1 | 0 | 0 | 0 | 0 | PD |
Fujita et al., 201814 | Japan | Retrospective | 2015.12–2018.3 | 12 | 66.7 | 70.8 | Nivo | Second∼ | 41.7 | 6.2 | 0 | 7 | 2 | 3 | 0 | 2 | PD |
Niki et al., 201815 | Japan | Retrospective | 2015.12–2017.12 | 11 | 81.8 | 66 | Nivo | NR | NR | 4.9 | 0 | 5 | 2 | 4 | 0 | 0 | PD |
Santini et al., 201816 | America | Retrospective | 2011.4–2016.5 | 38 | 52.6 | 64 | Anti–PD(L)1/anti-CTLA4 | First∼ | NR | NR | 18 | 20 | 0 | 6 | irAE | ||
Fujita et al., 201917 | Japan | Retrospective | 2018.1–2018.12 | 18 | 61.1 | 71 | Nivo/Pemb | Second | 50 | NR | 0 | 8 | 4 | 5 | 1 | 0 | NR |
Watanabe et al., 201918 | Japan | Retrospective | 2015.12–2017.12 | 14 | 57.1 | 61.5 | Atezo/nivo/pemb | NR | 50 | 3.7 | 0 | 3 | 5 | 6 | 0 | 0 | PD |
Mouri et al., 201919 | Japan | Retrospective | 2015.12–2018.8 | 21 | 90.5 | 69.6 | Nivo | Second∼ | NR | 13.3 | 1 | 12 | 8 | 0 | 0 | 7 | irAE |
Fujita et al., 202020 | Japan | Retrospective | 2018.1–2019.8 | 15 | 93.3 | 71.4 | Atezo/durva | Second∼ | 0 | 3 | 0 | 0 | 5 | 9 | 1 | 0 | PD |
Gobbini et al., 202021 | France | Retrospective | 2010–2018 | 144 | 67.4 | 63 | Anti–PD-(L)1 | First∼ | 14.6 | 13 | 10 | 61 | 38 | 26 | 9 | 27 | irAE, PD, clinical decision |
Herbst et al., 202022 | Keynote 10 | Retrospective | 2013.8–2015.2 | 14 | NR | NR | Pemb | First∼ | NR | NR | 0 | 13 | 0 | 0 | 1 | NR | Clinical decision |
Katayama et al., 202023 | Japan | Retrospective | 2017.4–2018.11 | 35 | 68.6 | 70 | Nivo/pemb/atezo | Third | 40 | 4 | 0 | 12 | 12 | 10 | 1 | NR | PD |
Kitagawa et al., 202024 | Japan | Retrospective | 2018.4–2019.9 | 17 | 64.7 | 69 | Anti–PD-(L)1 | First∼ | 17.6 | 9.7 | 0 | 6 | 9 | 2 | 0 | 3 | PD |
Furuya et al., 202125 | Japan | Retrospective | 2018.4–2019.2 | 38 | NR | NR | Nivo/pemb | Second∼ | NR | NR | 0 | 8 | 16 | 11 | 3 | NR | irAE, PD |
Takahara et al., 202226 | Japan | Retrospective | 2016.8–2021.7 | 24 | 66.7 | NR | Durva/pemb/nivo | NR | 45.8 | NR | NR | 4 | irAE, PD | ||||
Xu et al., 202227 | People's Republic of China | Retrospective | 2018.12–2021.6 | 40 | 77.5 | NR | Anti–PD-1 | NR | NR | 5.7 | 0 | 14 | 19 | 7 | 0 | NR | PD |
Study | Interval Time (Median mo) | ICI Rechallenge |
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---|---|---|---|---|---|---|---|---|---|---|---|
Regimen(r) | Therapy Line | TPS ≥ 50% (%)a | PFSr (M) | Best Response |
G3/4 irAE | ||||||
CR | PR | Stable Disease | PD | NR | |||||||
Bernard et al., 201813 | 10 | Anti–PD-(L)1 | NR | NR | 35.4 | 0 | 0 | 1 | 0 | 0 | 0 |
Fujita et al., 201814 | NR | Pemb | NR | 50 | 3.1 | 0 | 1 | 4 | 6 | 1 | 0 |
Niki et al., 201815 | 4.2 | Nivo/pemb | NR | NR | 2.7 | 0 | 3 | 2 | 6 | 0 | 0 |
Santini et al., 201816 | NR | Anti–PD-(L)1/anti–CTLA4 | NR | NR | NR | NR | 8 | ||||
Fujita et al., 201917 | NR | Atezo | Third∼ | NR | NR | 0 | 0 | 7 | 11 | 0 | 2 |
Watanabe et al., 201918 | 6.5 | Atezo/nivo/pemb | NR | NR | 1.6 | 0 | 1 | 2 | 11 | 0 | 0 |
Mouri et al., 201919 | NR | Nivo | NR | NR | 7.4 | 0 | 4 | 14 | 2 | 1 | 2 |
Fujita et al., 202020 | NR | Nivo/pemb | NR | NR | 2.4 | 0 | 0 | 4 | 9 | 2 | 2 |
Gobbini et al., 202021 | NR | Anti–PD-(L)1 | Second∼ | NR | 4.4 | 5 | 18 | 45 | 54 | 22 | 4 |
Herbst et al., 202022 | NR | Pemb | NR | NR | NR | 0 | 6 | 5 | 2 | 1 | NR |
Katayama et al., 202023 | 5.2 | Nivo/pemb/atezo | Fourth | NR | 2.7 | 0 | 1 | 14 | 18 | 2 | NR |
Kitagawa et al., 202024 | NR | Anti–PD-(L)1 | Second∼ | NR | 4 | 0 | 1 | 9 | 7 | 0 | 2 |
Furuya et al., 202125 | NR | Atezo | NR | NR | NR | 0 | 1 | 12 | 20 | 5 | NR |
Takahara et al., 202226 | NR | Nivo/atezo/pemb | NR | NR | NR | 0 | 2 | 9 | 13 | 0 | 3 |
Xu et al., 202227 | NR | Anti–PD-1 | NR | NR | 6.8 | 0 | 9 | 25 | 6 | 0 | NR |
Anti–PD-(L)1, immune checkpoint blockade targeting programmed cell death-(ligand)1; Atezo, atezolizumab; CR, complete response; Durva, durvalumab; G3/4 irAE, grade 3/4 immune-related adverse event; ICI, immune checkpoint inhibitor; Nivo, nivolumab; NR, not reported; PD, progressive disease; Pemb, pembrolizumab; PFSi, progression-free survival of initial ICI; PFSr, progression-free survival of ICI rechallenge; PR, partial response; Regimen(i), initial ICI regimen; Regimen(r), ICI rechallenge regimen; TPS, tumor proportion score.
Percentage of patients whose TPS is equals to or more than 50%.