Table 1.
First author | Year | Type of study | N | Grade of CIPN | Main types of antineoplastic drugs | Outcome measure | Type of cancer |
---|---|---|---|---|---|---|---|
Molassiotis A | 2019 [24] | Cohort | 255 | ≥ 1 | Platinum, taxane | NCI-CTCAE | Breast, lung, ovarian, gastrointestinal, head & neck, and urinary tract cancers |
Chen C | 2019 [16] | Cohort | 60 | ≥ 1 | Oxaliplatin | WHO standard | Colorectal, gastric, and esophageal cancers |
Hertz DL | 2018 [25] | Cohort | 60 | Self-report | Cisplatin | EORTC QLQ-CIPN20 | Breast cancer |
Gaballah A | 2018 [17] | Case–control | 250 | ≥ 1 | Platinum, taxane | NCI-CTCAE | NA |
Yamaguchi K | 2018 [26] | Cohort | 60 | ≥ 2 | Oxaliplatin | NCI-CTCAE | Gastric cancer |
Dolan ME | 2017 [27] | Cohort | 680 | Self-report | Cisplatin | EORTC QLQ-CIPN20 | germ cell cancer |
Song SJ | 2017 [28] | Case–control | 1516 | ≥ 2 | Taxane | Cancer pain management guideline, 6th edition | Breast cancer |
Hershman DL | 2016 [23] | Case–control | 1401 | ≥ 2 | Multiple chemotherapy regimens | NCI-CTCAE | lung, prostate, breast, head and neck, bladder, and ovarian cancers |
Bao T | 2016 [29] | Case–control | 296 | ≥ 1 | Taxane | Cancer-related symptom rating scales | Breast cancer |
Tanishima H | 2016 [30] | Case–control | 47 | ≥ 1 | Oxaliplatin | NCI-CTCAE | Colorectal cancer |
Pereira S | 2016 [31] | Cohort | 296 | ≥ 1 | Taxane | NCI-CTCAE | Breast cancer |
Wang YQ | 2016 [18] | Case–control | 225 | ≥ 2 | Oxaliplatin, paclitaxel, vincristine | NCI-CTCAE | Colorectal, gastric, esophageal, lung, and ovarian cancers; lymphoma |
Shahriari-Ahmadi A | 2015 [32] | Case–control | 130 | ≥ 1 | Oxaliplatin | NCI-CTCAE | Colorectal cancer |
Kus Ta | 2015 [15] | Case–control | 270 | ≥ 1 | Taxane | NCI-CTCAE | NA |
Kus Ta | 2015 [15] | Case–control | 104 | ≥ 1 | Taxane, platinum | NCI-CTCAE | NA |
de la Morena Barrio P | 2015 [19] | Case–control | 129 | ≥ 1 | Paclitaxel | NCI-CTCAE | Breast cancer |
Ding XF | 2015 [20] | Cohort | 94 | ≥ 1 | Paclitaxel | Self-definition | Prostate, breast, ovarian, bladder, lung, and cervical cancers |
Johnson Cb | 2015 [21] | Case–control | 735 | ≥ 1 | Platinum, taxane | NCI-CTCAE | Lung cancer |
Eckhoff L | 2014 [33] | Cohort | 150 | ≥ 2 | Docetaxel | NCI-CTCAE | Breast cancer |
Xue YJ | 2013 [22] | Cohort | 80 | ≥ 1 | Paclitaxel | Levi | Breast, lung, esophageal, gastric, ovarian, and uterine cancers |
Wang XY | 2013 [34] | Case–control | 171 | ≥ 2 | Oxaliplatin | Levi | Colorectal cancer |
Hashimoto N | 2012 [35] | Case–control | 48 | ≥ 2 | Bortezomib | NCI-CTCAE | Multiple myeloma |
Kawakami K | 2012 [36] | Case–control | 50 | ≥ 3 | Paclitaxel, carboplatin | NCI-CTCAE | Non-small cell lung cancer |
Vincenzi B | 2012 [37] | Case–control | 169 | ≥ 2 | Oxaliplatin | NCI-CTCAE | Colorectal cancer |
Uwah AN | 2012 [38] | Case–control | 62 | ≥ 2 | Oxaliplatin | NCI-CTCAE | Colorectal cancer |
Ramanathan RK | 2010 [39] | Case–control | 1585 | ≥ 1 | Oxaliplatin | NCI-CTCAE, oxaliplatin-specific neurotoxicity scale | Colorectal cancer |
NCI-CTCAE National Cancer Institute-Common Toxicity Criteria for Adverse Events; EORTC QLQ-CIPN20 European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Chemotherapy-Induced Peripheral Neuropathy; CIPN chemotherapy-induced peripheral neuropathy
aThe incidence of CIPN was clearly distinguished between the two treatment schemes
bPatients with unknown CIPN status were excluded from statistical analysis