TY - JOUR
T1 - Clinical impact of probiotics on the efficacy of anti-PD-1 monotherapy in patients with nonsmall cell lung cancer
T2 - A multicenter retrospective survival analysis study with inverse probability of treatment weighting
AU - Takada, Kazuki
AU - Shimokawa, Mototsugu
AU - Takamori, Shinkichi
AU - Shimamatsu, Shinichiro
AU - Hirai, Fumihiko
AU - Tagawa, Tetsuzo
AU - Okamoto, Tatsuro
AU - Hamatake, Motoharu
AU - Tsuchiya-Kawano, Yuko
AU - Otsubo, Kohei
AU - Inoue, Koji
AU - Yoneshima, Yasuto
AU - Tanaka, Kentaro
AU - Okamoto, Isamu
AU - Nakanishi, Yoichi
AU - Mori, Masaki
N1 - Publisher Copyright:
© 2021 UICC
PY - 2021/7/15
Y1 - 2021/7/15
N2 - The gastrointestinal microbiota was reported as an important factor for the response to cancer immunotherapy. Probiotics associated with gastrointestinal dysbiosis and bacterial richness may affect the efficacy of cancer immunotherapy drugs. However, the clinical impact of probiotics on the efficacy of cancer immunotherapy in patients with nonsmall cell lung cancer (NSCLC) is poorly understood. The outcomes of 294 patients with advanced or recurrent NSCLC who received antiprogrammed cell death-1 (PD-1) therapy (nivolumab or pembrolizumab monotherapy) at three medical centers in Japan were analyzed in our study. We used inverse probability of treatment weighting (IPTW) to minimize the bias arising from the patients' backgrounds. The IPTW-adjusted Kaplan-Meier curves showed that progression-free survival (nonuse vs use: hazard ratio [HR] [95% confidence interval {CI}] = 1.73 [1.42-2.11], log-rank test P =.0229), but not overall survival (nonuse vs use: HR [95%CI] = 1.40 [1.13-1.74], log-rank test P =.1835), was significantly longer in patients who received probiotics. Moreover, the IPTW-adjusted univariate analyses showed that nonuse or use of probiotics was significantly associated with disease control (nonuse vs use: odds ratio [OR] [95%CI] = 0.51 [0.35-0.74], P =.0004) and overall response (nonuse vs use: OR [95%CI] = 0.43 [0.29-0.63], P <.0001). In this multicenter and retrospective study, probiotics use was associated with favorable clinical outcomes in patients with advanced or recurrent NSCLC who received anti-PD-1 monotherapy. The findings should be validated in a future prospective study.
AB - The gastrointestinal microbiota was reported as an important factor for the response to cancer immunotherapy. Probiotics associated with gastrointestinal dysbiosis and bacterial richness may affect the efficacy of cancer immunotherapy drugs. However, the clinical impact of probiotics on the efficacy of cancer immunotherapy in patients with nonsmall cell lung cancer (NSCLC) is poorly understood. The outcomes of 294 patients with advanced or recurrent NSCLC who received antiprogrammed cell death-1 (PD-1) therapy (nivolumab or pembrolizumab monotherapy) at three medical centers in Japan were analyzed in our study. We used inverse probability of treatment weighting (IPTW) to minimize the bias arising from the patients' backgrounds. The IPTW-adjusted Kaplan-Meier curves showed that progression-free survival (nonuse vs use: hazard ratio [HR] [95% confidence interval {CI}] = 1.73 [1.42-2.11], log-rank test P =.0229), but not overall survival (nonuse vs use: HR [95%CI] = 1.40 [1.13-1.74], log-rank test P =.1835), was significantly longer in patients who received probiotics. Moreover, the IPTW-adjusted univariate analyses showed that nonuse or use of probiotics was significantly associated with disease control (nonuse vs use: odds ratio [OR] [95%CI] = 0.51 [0.35-0.74], P =.0004) and overall response (nonuse vs use: OR [95%CI] = 0.43 [0.29-0.63], P <.0001). In this multicenter and retrospective study, probiotics use was associated with favorable clinical outcomes in patients with advanced or recurrent NSCLC who received anti-PD-1 monotherapy. The findings should be validated in a future prospective study.
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U2 - 10.1002/ijc.33557
DO - 10.1002/ijc.33557
M3 - Article
C2 - 33720422
AN - SCOPUS:85103259552
SN - 0020-7136
VL - 149
SP - 473
EP - 482
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 2
ER -