Segal Neil H, Gada Purvi, Senzer Neil, Gargano Michele A, Patchen Myra L, Saltz Leonard B
Memorial Sloan Kettering Cancer Center, New York, NY.
University of Minnesota, Minneapolis, MN.
Clin Colorectal Cancer. 2016 Sep;15(3):222-7. doi: 10.1016/j.clcc.2016.02.013. Epub 2016 Feb 13.
Imprime PGG (β(1,6)-[poly-(1,3)-D-glucopyranosyl]-poly-β(1,3)-D-glucopyranose) is an innate immune cell modulator that primes neutrophils and monocytes/macrophages to exert antitumor activity against complement opsonized tumor cells. In patients with KRAS-mutant colorectal cancer (CRC), cetuximab alone is ineffective; however, it can bind to tumor cells and induce opsonization for recognition by Imprime PGG-bound innate immune cells. The primary objective of this study was to determine the antitumor activity of Imprime PGG in combination with cetuximab in patients with KRAS-mutant metastatic CRC.
The study had a 2-stage Simon optimal design with 80% power to detect a target objective response rate (ORR) of ≥10% at a 10% significance level. Patients received weekly Imprime PGG (4 mg/kg) and cetuximab (loading dose, 400 mg/m(2), then 250 mg/m(2)) intravenously. The primary end point was ORR; secondary end points included duration of response (DOR), time to progression (TTP), overall survival (OS), disease control rate, progression-free survival, and safety. Stage 1 of the study was to enroll 17 evaluable patients.
One partial response (5.6%) was observed among 18 patients enrolled into stage 1. Median DOR was 4.2 months, TTP 2.7 months, and OS 6.6 months. Overall, observed toxicity was as expected from cetuximab alone. The most common (≥20%) adverse events related to Imprime PGG were fatigue (7 patients; 38.9%), infusion reaction (4 patients; 22.2%), and headache (4 patients; 22.2%). There was no Grade 4 toxicity nor treatment-related deaths.
Imprime PGG in combination with cetuximab treatment in patients with KRAS-mutant CRC showed compelling, albeit modest, clinical activity. This study provides proof of principle that Imprime PGG, in combination with complement-activating antibodies, is associated with clinical activity.
Imprime PGG(β(1,6)-[聚-(1,3)-D-吡喃葡萄糖基]-聚-β(1,3)-D-吡喃葡萄糖)是一种先天性免疫细胞调节剂,可使中性粒细胞和单核细胞/巨噬细胞发挥对补体调理肿瘤细胞的抗肿瘤活性。在KRAS突变型结直肠癌(CRC)患者中,单独使用西妥昔单抗无效;然而,它可与肿瘤细胞结合并诱导调理作用,以供与Imprime PGG结合的先天性免疫细胞识别。本研究的主要目的是确定Imprime PGG联合西妥昔单抗对KRAS突变型转移性CRC患者的抗肿瘤活性。
本研究采用两阶段西蒙最优设计,在10%的显著性水平下,有80%的把握度检测到目标客观缓解率(ORR)≥10%。患者每周静脉注射Imprime PGG(4mg/kg)和西妥昔单抗(负荷剂量400mg/m²,随后250mg/m²)。主要终点为ORR;次要终点包括缓解持续时间(DOR)、疾病进展时间(TTP)、总生存期(OS)、疾病控制率、无进展生存期和安全性。研究的第1阶段纳入17例可评估患者。
第1阶段纳入的18例患者中观察到1例部分缓解(5.6%)。中位DOR为4.2个月,TTP为2.7个月,OS为6.6个月。总体而言,观察到的毒性与单独使用西妥昔单抗时预期的一致。与Imprime PGG相关的最常见(≥20%)不良事件为疲劳(7例患者;38.9%)、输注反应(4例患者;22.2%)和头痛(4例患者;22.2%)。无4级毒性反应,也无治疗相关死亡。
Imprime PGG联合西妥昔单抗治疗KRAS突变型CRC患者显示出令人信服的临床活性,尽管较为适度。本研究提供了原理证明,即Imprime PGG与补体激活抗体联合使用与临床活性相关。