共 2 条
Augmenting antibody response to EGF-depleting immunotherapy: Findings from a phase I trial of CIMAvax-EGF in combination with nivolumab in advanced stage NSCLC
被引:6
|作者:
Evans, Rachel
[1
]
Lee, Kelvin
[2
]
Wallace, Paul K.
[1
]
Reid, Mary
[1
]
Muhitch, Jason
[1
]
Dozier, Askia
[1
]
Mesa, Circe
[3
]
Luaces, Patricia L.
[3
]
Santos-Morales, Orestes
[3
]
Groman, Adrienne
[1
]
Cedeno, Carlos
[1
]
Cinquino, Aileen
[1
]
Fisher, Daniel T.
[1
]
Puzanov, Igor
[1
]
Opyrchal, Mateusz
[2
]
Fountzilas, Christos
[1
]
Dai, Tong
[1
]
Ernstoff, Marc
[4
]
Attwood, Kristopher
[1
]
Hutson, Alan
[1
]
Johnson, Candace
[1
]
Mazorra, Zaima
[3
]
Saavedra, Danay
[3
]
Leon, Kalet
[3
]
Lage, Agustin
[3
]
Crombet, Tania
[3
]
Dy, Grace K.
[1
]
机构:
[1] Roswell Pk Comprehens Canc Ctr, Buffalo, NY 14203 USA
[2] Indiana Univ, Dept Med, Melvin & Bren Simon Comprehens Canc Ctr, Indianapolis, IN USA
[3] Ctr Immunol Mol, Havana, La Habana, Cuba
[4] Natl Canc Inst NCI, Div Canc Treatment & Diag, Bethesda, MD USA
来源:
FRONTIERS IN ONCOLOGY
|
2022年
/
12卷
关键词:
immunotherapy;
lung cancer;
non-small cell lung cancer;
immune checkpoint inhibitor;
vaccine;
LONG-TERM SURVIVAL;
LUNG-CANCER;
CHECKMATE;
017;
VACCINE;
DOCETAXEL;
OUTCOMES;
THERAPY;
BURDEN;
PD-1;
D O I:
10.3389/fonc.2022.958043
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BackgroundCIMAvax-EGF is an epidermal growth factor (EGF)-depleting immunotherapy which has shown survival benefit as a switch maintenance treatment after platinum-based chemotherapy in advanced non-small cell lung cancer (NSCLC). The primary objective of this trial is to establish the safety and recommended phase II dose (RP2D) of CIMAvax-EGF in combination with nivolumab as second-line therapy for NSCLC. MethodsPatients with immune checkpoint inhibitor-naive metastatic NSCLC were enrolled using a "3+3" dose-escalation design. Toxicities were graded according to CTCAE V4.03. Thirteen patients (one unevaluable), the majority with PD-L1 0%, were enrolled into two dose levels of CIMAvax-EGF. FindingsThe combination was determined to be safe and tolerable. The recommended phase 2 dose of CIMAvax-EGF was 2.4 mg. Humoral response to CIMAvax-EGF was achieved earlier and in a greater number of patients with the combination compared to historical control. Four out of 12 evaluable patients had an objective response.
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页数:11
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