Neoadjuvant nivolumab with or without relatlimab in resectable non-small-cell lung cancer: a randomized phase 2 trial

被引:21
作者
Schuler, Martin [1 ,2 ,3 ]
Cuppens, Kristof [4 ,5 ]
Ploenes, Till [2 ,6 ,18 ]
Wiesweg, Marcel [1 ,2 ,3 ]
Du Pont, Bert [7 ]
Hegedus, Balazs [2 ,6 ]
Koester, Johannes [2 ,3 ,8 ]
Mairinger, Fabian [2 ,9 ]
Darwiche, Kaid [2 ,3 ,10 ]
Paschen, Annette [2 ,11 ]
Maes, Brigitte [12 ]
Vanbockrijck, Michel [13 ]
Laehnemann, David [1 ,2 ,8 ]
Zhao, Fang [2 ,11 ]
Hautzel, Hubertus [2 ,3 ,14 ]
Theegarten, Dirk [2 ,9 ]
Hartemink, Koen [15 ]
Reis, Henning [2 ,9 ,16 ]
Baas, Paul [17 ]
Schramm, Alexander [1 ,2 ]
Aigner, Clemens [2 ,6 ,19 ]
机构
[1] Univ Hosp Essen, West German Canc Ctr, Dept Med Oncol, Essen, Germany
[2] Univ Duisburg Essen, Med Fac, Essen, Germany
[3] Natl Ctr Tumor Dis NCT West, Essen, Germany
[4] Jessa Hosp, Dept Pulmonol & Thorac Oncol & Jessa & Sci, Hasselt, Belgium
[5] UHasselt, Fac Med & Life Sci, LCRC, Diepenbeek, Belgium
[6] Univ Med Essen, Ruhrlandklin, West German Canc Ctr, Dept Thorac Surg, Essen, Germany
[7] Jessa Hosp, Dept Thorac & Vasc Surg, Hasselt, Belgium
[8] Univ Hosp Essen, Inst Artificial Intelligence Med, Bioinformat & Computat Oncol, Essen, Germany
[9] Univ Hosp Essen, Inst Pathol, West German Canc Ctr, Essen, Germany
[10] Univ Med Essen, West German Canc Ctr, Dept Pulm Med, Ruhrlandklin, Essen, Germany
[11] Univ Hosp Essen, West German Canc Ctr, Dept Pathol, Essen, Germany
[12] Jessa Hosp, Lab Med Dept, Lab Mol Diagnost, Hasselt, Belgium
[13] Jessa Hosp, Dept Pathol, Hasselt, Belgium
[14] Univ Hosp Essen, West German Canc Ctr, Dept Nucl Med, Essen, Germany
[15] Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Surg, Amsterdam, Netherlands
[16] Goethe Univ, Univ Hosp Frankfurt, Dr Senckenberg Inst Pathol, Frankfurt, Germany
[17] Antoni Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Thorac Oncol, Amsterdam, Netherlands
[18] Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Dept Surg, Div Thorac Surg, Dresden, Germany
[19] Med Univ Vienna, Gen Hosp Vienna, Dept Thorac Surg, Vienna, Austria
关键词
OPEN-LABEL; PEMBROLIZUMAB; CHEMOTHERAPY; ADJUVANT;
D O I
10.1038/s41591-024-02965-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antibodies targeting the immune checkpoint molecules PD-1, PD-L1 and CTLA-4, administered alone or in combination with chemotherapy, are the standard of care in most patients with metastatic non-small-cell lung cancers. When given before curative surgery, tumor responses and improved event-free survival are achieved. New antibody combinations may be more efficacious and tolerable. In an ongoing, open-label phase 2 study, 60 biomarker-unselected, treatment-naive patients with resectable non-small-cell lung cancer were randomized to receive two preoperative doses of nivolumab (anti-PD-1) with or without relatlimab (anti-LAG-3) antibody therapy. The primary study endpoint was the feasibility of surgery within 43 days, which was met by all patients. Curative resection was achieved in 95% of patients. Secondary endpoints included pathological and radiographic response rates, pathologically complete resection rates, disease-free and overall survival rates, and safety. Major pathological (<= 10% viable tumor cells) and objective radiographic responses were achieved in 27% and 10% (nivolumab) and in 30% and 27% (nivolumab and relatlimab) of patients, respectively. In 100% (nivolumab) and 90% (nivolumab and relatlimab) of patients, tumors and lymph nodes were pathologically completely resected. With 12 months median duration of follow-up, disease-free survival and overall survival rates at 12 months were 89% and 93% (nivolumab), and 93% and 100% (nivolumab and relatlimab). Both treatments were safe with grade >= 3 treatment-emergent adverse events reported in 10% and 13% of patients per study arm. Exploratory analyses provided insights into biological processes triggered by preoperative immunotherapy. This study establishes the feasibility and safety of dual targeting of PD-1 and LAG-3 before lung cancer surgery.ClinicalTrials.gov Indentifier: NCT04205552. In an open-label phase 2 trial, patients with non-small-cell lung cancer received neoadjuvant anti-PD-1 with or without anti-LAG-3, showing that curative intent surgery after combined blockade of PD-1 and LAG-3 is feasible, and leads to preliminary clinical responses.
引用
收藏
页码:1602 / 1611
页数:25
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