Anti-PD-1 Therapy plus Chemotherapy and/or Bevacizumab as Second Line or later Treatment for Patients with Advanced Non-Small Cell Lung Cancer
Anti-PD-1 Therapy plus Chemotherapy and/or Bevacizumab as Second Line or later Treatment for Patients with Advanced Non-Small Cell Lung Cancer
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抗 PD-1 疗法联合化疗和/或贝伐珠单抗作为晚期非小细胞肺癌患者的二线或后续治疗
DOI:
10.7150/jca.37966
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发表时间:
2020-01
影响因子:
3.9
通讯作者:
Hu Yi
中科院分区:
文献类型:
--
作者:
Zhang Fan;Huang Di;Li Tao;Zhang Sujie;Wang Jinliang;Zhang Yuzi;Wang Guoqiang;Zhao Zhengyi;Ma Junxun;Wang Lijie;Sun Danyang;Cui Pengfei;Cai Shangli;Jiao Shunchang;Zhao Lei;Hu Yi
Immune checkpoint inhibitor combination therapy exhibited outstanding efficacy in first line setting for advanced non-small cell lung cancer (aNSCLC) patients. However, whether PD-1 inhibitor combined treatment is effective in second line or later setting remains unknown. Therefore, we retrospectively evaluated the efficacy of combined therapy of PD-1 inhibitor with chemotherapy and/or bevacizumab compared to PD-1 inhibitor alone for aNSCLC patients in second line or later setting. Patients with aNSCLC who have received anti-PD-1 based therapy between 2015 and 2017 were screened, and 55 patients were ultimately included and divided into the monotherapy group (N=33) and the combination group (N=22). Patients treated with combination therapy exhibited superior PFS versus those treated with monotherapy (median PFS, 7.5 months vs 3.3 months; hazard ratio 0.28; 95% CI, 0.14-0.56; P<0.001). Objective response rate and disease control rate were 31.8% (7/22) and 95.5% (21/22) in the combination group and 10.0% (3/30) and 46.7% (14/30) in the monotherapy group, respectively (ORR, P=0.075; DCR, P<0.001). Five patients (22.7%) experienced grade 3-4 adverse events in the combination group and two patients (6.1%) in the monotherapy group. Taken together, our results indicated that for NSCLC patients who had failed on the first-line or later treatment, PD-1 inhibitor in combination with chemotherapy and/or bevacizumab might be a favorable treatment option. These findings warrant further validation in prospective studies.
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影响因子:
5.6
作者:
Pircher A;Wolf D;Heidenreich A;Hilbe W;Pichler R;Heidegger I
通讯作者:
Heidegger I
影响因子:
8.8
作者:
通讯作者:
--
影响因子:
10.1
作者:
Hodi FS;Lawrence D;Lezcano C;Wu X;Zhou J;Sasada T;Zeng W;Giobbie-Hurder A;Atkins MB;Ibrahim N;Friedlander P;Flaherty KT;Murphy GF;Rodig S;Velazquez EF;Mihm MC Jr;Russell S;DiPiro PJ;Yap JT;Ramaiya N;Van den Abbeele AD;Gargano M;McDermott D
通讯作者:
McDermott D
DOI:
10.1158/1078-0432.ccr-15-3101
发表时间:
2016-09-15
期刊:
Clinical cancer research : an official journal of the American Association for Cancer Research
影响因子:
--
作者:
Gainor JF;Shaw AT;Sequist LV;Fu X;Azzoli CG;Piotrowska Z;Huynh TG;Zhao L;Fulton L;Schultz KR;Howe E;Farago AF;Sullivan RJ;Stone JR;Digumarthy S;Moran T;Hata AN;Yagi Y;Yeap BY;Engelman JA;Mino-Kenudson M
通讯作者:
Mino-Kenudson M
影响因子:
45.3
作者:
Rizvi, Naiyer A.;Hellmann, Matthew D.;Antonia, Scott
通讯作者:
Antonia, Scott