Is the Efficacy of Adding Ramucirumab to Docetaxel Related to a History of Immune Checkpoint Inhibitors in the Real-World Clinical Practice?
被引:6
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作者:
Nishimura, Tadashi
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Mie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Mie Univ, Grad Sch Med, Dept Pulm & Crit Care Med, Tsu, Mie 5148507, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Nishimura, Tadashi
[1
,2
]
Fujimoto, Hajime
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Mie Univ, Grad Sch Med, Dept Pulm & Crit Care Med, Tsu, Mie 5148507, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Fujimoto, Hajime
[2
]
Okano, Tomohito
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Mie Univ, Grad Sch Med, Dept Pulm & Crit Care Med, Tsu, Mie 5148507, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Okano, Tomohito
[2
]
Naito, Masahiro
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Mie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Naito, Masahiro
[1
]
Tsuji, Chikashi
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Mie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Tsuji, Chikashi
[1
]
Iwanaka, Soichi
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Mie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Iwanaka, Soichi
[1
]
Sakakura, Yasumasa
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Mie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Sakakura, Yasumasa
[1
]
Yasuma, Taro
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Mie Univ, Grad Sch Med, Dept Immunol, Tsu, Mie 5148507, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Yasuma, Taro
[3
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D'Alessandro-Gabazza, Corina N.
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Mie Univ, Grad Sch Med, Dept Immunol, Tsu, Mie 5148507, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
D'Alessandro-Gabazza, Corina N.
[3
]
Oomoto, Yasuhiro
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Mie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Oomoto, Yasuhiro
[1
]
Gabazza, Esteban C.
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Mie Univ, Grad Sch Med, Dept Immunol, Tsu, Mie 5148507, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Gabazza, Esteban C.
[3
]
Kobayashi, Tetsu
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Mie Univ, Grad Sch Med, Dept Pulm & Crit Care Med, Tsu, Mie 5148507, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Kobayashi, Tetsu
[2
]
Ibata, Hidenori
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Mie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, JapanMie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
Ibata, Hidenori
[1
]
机构:
[1] Mie Chuo Med Ctr, Dept Pulm Med, Tsu, Mie 5141101, Japan
[2] Mie Univ, Grad Sch Med, Dept Pulm & Crit Care Med, Tsu, Mie 5148507, Japan
[3] Mie Univ, Grad Sch Med, Dept Immunol, Tsu, Mie 5148507, Japan
Simple Summary Previous studies have shown that the use of chemotherapy in combination with immune checkpoint inhibitors as a first-line treatment in patients with non-small cell lung cancer improved overall survival and progression-free survival. However, the efficacy of cytotoxic agents as a second-line or later-line therapy in non-small cell lung cancer patients previously treated with immune checkpoint inhibitors in the real-world clinical practice is still controversial. In the present study, we retrospectively evaluated patients with non-small cell lung cancer to clarify whether the previous treatment with immune checkpoint inhibitors impacts the efficacy of docetaxel or the combined therapy of docetaxel plus ramucirumab. The results of this study using real-world data show that the addition of ramucirumab to docetaxel is superior to docetaxel monotherapy for improving time-to-treatment failure and overall survival, irrespective of previous treatment with immune checkpoint inhibitors. Reports on the efficacy of second-line treatment with cytotoxic agents after treatment with immune checkpoint inhibitors are limited. Here, we retrospectively evaluated patients in the real-world clinical practice treated with docetaxel or docetaxel plus ramucirumab. Ninety-three patients treated with docetaxel or docetaxel plus ramucirumab as a second- or later-line therapy were included. The patients were categorized into the following four treatment groups: docetaxel group (n = 50), docetaxel/ramucirumab group (n = 43) and pretreated (n = 45) and untreated (n = 48) with immune checkpoint inhibitor groups. The docetaxel/ramucirumab group showed an overall response rate of 57.1% in patients pretreated with immune checkpoint inhibitors and 20% in untreated patients. The docetaxel group showed an overall response rate of 15.4% in patients pretreated with immune checkpoint inhibitors and 5.0% in untreated patients. The median time-to-treatment failure and the median survival time were longer in the docetaxel/ramucirumab group than in the docetaxel group in both immune checkpoint inhibitor-pretreated and -untreated groups. There was no difference in time-to-treatment failure and overall survival between immune checkpoint inhibitor-pretreated and -untreated groups in each docetaxel and docetaxel/ramucirumab treatment group. In conclusion, our real-world data show that the addition of ramucirumab to docetaxel was superior to docetaxel monotherapy for improving time-to-treatment failure and overall survival, irrespective of previous treatment with immune checkpoint inhibitors.
机构:
Univ Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USAUniv Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USA
Muchnik, Eugene
Loh, Kah Poh
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Univ Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USAUniv Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USA
Loh, Kah Poh
Strawderman, Myla
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机构:
Univ Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USAUniv Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USA
Strawderman, Myla
Magnuson, Allison
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Univ Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USAUniv Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USA
Magnuson, Allison
Mohile, Supriya G.
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Univ Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USAUniv Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USA
Mohile, Supriya G.
Estrah, Vered
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机构:
Mackenzie Hlth, Richmond Hill, ON, CanadaUniv Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USA
Estrah, Vered
Maggiore, Ronald J.
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Univ Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USAUniv Rochester, James P Wilmot Canc Inst, Med Ctr, Rochester, NY 14642 USA
机构:
Michigan Med, Dept Pharm Serv & Clin Sci, Ann Arbor, MI USA
Univ Michigan, Coll Pharm, 428 Church St, Ann Arbor, MI 48109 USAMichigan Med, Dept Pharm Serv & Clin Sci, Ann Arbor, MI USA
Weis, Taylor M.
Hough, Shannon
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机构:
Michigan Med, Dept Pharm Serv & Clin Sci, Ann Arbor, MI USA
Univ Michigan, Coll Pharm, 428 Church St, Ann Arbor, MI 48109 USAMichigan Med, Dept Pharm Serv & Clin Sci, Ann Arbor, MI USA
Hough, Shannon
Reddy, Haritha G.
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Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI USAMichigan Med, Dept Pharm Serv & Clin Sci, Ann Arbor, MI USA
Reddy, Haritha G.
Daignault-Newton, Stephanie
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Univ Michigan, Sch Publ Hlth, Dept Biostat, Ctr Canc Biostat, Ann Arbor, MI 48109 USAMichigan Med, Dept Pharm Serv & Clin Sci, Ann Arbor, MI USA
Daignault-Newton, Stephanie
Kalemkerian, Gregory P.
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Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI USAMichigan Med, Dept Pharm Serv & Clin Sci, Ann Arbor, MI USA