TY - JOUR
T1 - Predictive and prognostic impact of primary tumor-bearing lobe in nonsmall cell lung cancer patients treated with anti-PD-1 therapy
AU - Takamori, Shinkichi
AU - Takada, Kazuki
AU - Shimokawa, Mototsugu
AU - Matsubara, Taichi
AU - Haratake, Naoki
AU - Miura, Naoko
AU - Toyozawa, Ryo
AU - Yamaguchi, Masafumi
AU - Takenoyama, Mitsuhiro
AU - Yoneshima, Yasuto
AU - Tanaka, Kentaro
AU - Okamoto, Isamu
AU - Tagawa, Tetsuzo
AU - Mori, Masaki
N1 - Funding Information:
As a potential personal and financial conflict of interest, Mr. Shimokawa reports personal fees from Sysmex. Dr Toyozawa reports personal fees from Kyowa Hakko Kirin Co., Ltd., Nippon Kayaku Co., Ltd., Novartis Pharma K.K. and grants from Abbvie, Daiichi Sankyo Co. Ltd., Pfizer Japan, Takeda Pharmaceutical Co. Ltd. Dr Yamaguchi reports personal fees from AstraZeneca K.K., Nippon Boehringer Ingelheim Co., Ltd, Ono Pharmaceutical Co. Ltd., Taiho Pharmaceutical Co., Ltd. and grants from Chugai Pharmaceutical Co., Ltd., Pfizer Japan Inc. Dr Takenoyama reports personal fees from AstraZeneca K.K., Bristol‐Myers Squibb K.K, Chugai Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Johnson & Johnson, Kyowa Hakko Kirin Co., Ltd., MSD, Nippon Boehringer Ingelheim Co., Ltd, Nippon Kayaku Co., Ltd., Ono Pharmaceutical Co. Ltd., Taiho Pharmaceutical Co., Ltd., and grants from Chugai Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., MSD, Nippon Boehringer Ingelheim Co., Ltd, Novartis Pharma K.K., Ono Pharmaceutical Co. Ltd., Pfizer Japan Inc., Taiho Pharmaceutical Co., Ltd. Dr Tanaka reports personal fees from Astrazeneca, Chugai, Eli Lilly, Bristol Myers Squibb, Ono, Boehlinger Ingelheim, Abbvie, Novartis, Pfizer, KyowaKirin, MSD, and Taiho; grants from Chugai, Ono and Boehringer Ingelheim. Dr Okamoto reports grants and personal fees from AstraZeneca, grants and personal fees from Taiho Pharmaceutical, grants and personal fees from Boehringer Ingelheim, grants and personal fees from Ono Pharmaceutical, grants and personal fees from MSD Oncology, grants and personal fees from Lilly, grants from Astellas Pharma, grants and personal fees from Bristol‐Myers Squibb, grants from Novartis, grants and personal fees from Chugai Pharma, personal fees from Pfizer, grants from AbbVie. Dr Tagawa reports grants from Chugai Pharmaceutical Co., Ltd., Roche Diagnostics. Dr Mori reports grants from Chugai Pharmaceutical Co., Ltd. The other authors declare no conflicts of interest. All the authors declare no conflicts of interest in association with our study.
Publisher Copyright:
© 2020 UICC
PY - 2020/10/15
Y1 - 2020/10/15
N2 - Immunotherapy targeting programmed cell death-1 (PD-1) has become a standard pharmacological therapy. Although tumor mutation burden level was reported to depend on the tumor location in nonsmall cell lung cancer (NSCLC), predictive impact of the tumor location on the response to anti-PD-1 therapy is unknown. Two hundred and seventeen advanced or recurrent NSCLC patients treated with anti-PD-1 therapy at Kyushu University Hospital and National Hospital Organization Kyushu Cancer Center were analyzed. To minimize the bias arising from the patients’ background, adjusted Kaplan-Meier survival curves and Cox proportional hazards regression analyses using inverse probability of treatment weights (IPTW) were performed. Of the 217 patients, 132, 27, and 58 had primary NSCLC in upper, middle, and lower lobes, respectively. Patients with NSCLC in upper lobe were significantly associated with younger age (P =.0070) and smoker (P =.0003). The epidermal growth factor receptor-wild type and tumor location in upper lobe were independent predictors of disease control (P =.0175 and P =.0425, respectively). The IPTW-adjusted Kaplan-Meier curves showed that patients with NSCLC in the upper lobes had significantly longer progression-free survival (PFS) and overall survival (OS) than those in middle/lower lobes (P =.0026 and P =.0015, respectively). On IPTW adjusted Cox analysis, NSCLC in the upper lobe was an independent predictor of PFS and OS (P =.0078 and P =.0034, respectively). Patients with primary NSCLC in the upper lobes may be good candidates for anti-PD-1 therapy. These findings should be validated prospectively.
AB - Immunotherapy targeting programmed cell death-1 (PD-1) has become a standard pharmacological therapy. Although tumor mutation burden level was reported to depend on the tumor location in nonsmall cell lung cancer (NSCLC), predictive impact of the tumor location on the response to anti-PD-1 therapy is unknown. Two hundred and seventeen advanced or recurrent NSCLC patients treated with anti-PD-1 therapy at Kyushu University Hospital and National Hospital Organization Kyushu Cancer Center were analyzed. To minimize the bias arising from the patients’ background, adjusted Kaplan-Meier survival curves and Cox proportional hazards regression analyses using inverse probability of treatment weights (IPTW) were performed. Of the 217 patients, 132, 27, and 58 had primary NSCLC in upper, middle, and lower lobes, respectively. Patients with NSCLC in upper lobe were significantly associated with younger age (P =.0070) and smoker (P =.0003). The epidermal growth factor receptor-wild type and tumor location in upper lobe were independent predictors of disease control (P =.0175 and P =.0425, respectively). The IPTW-adjusted Kaplan-Meier curves showed that patients with NSCLC in the upper lobes had significantly longer progression-free survival (PFS) and overall survival (OS) than those in middle/lower lobes (P =.0026 and P =.0015, respectively). On IPTW adjusted Cox analysis, NSCLC in the upper lobe was an independent predictor of PFS and OS (P =.0078 and P =.0034, respectively). Patients with primary NSCLC in the upper lobes may be good candidates for anti-PD-1 therapy. These findings should be validated prospectively.
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U2 - 10.1002/ijc.33030
DO - 10.1002/ijc.33030
M3 - Article
C2 - 32356560
AN - SCOPUS:85086020770
SN - 0020-7136
VL - 147
SP - 2327
EP - 2334
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 8
ER -