Tanyi Janos L, Randall Leslie M, Chambers Setsuko K, Butler Kristina A, Winer Ira S, Langstraat Carrie L, Han Ernest S, Vahrmeijer Alexander L, Chon Hye Sook, Morgan Mark A, Powell Matthew A, Tseng Jill H, Lopez Alexis S, Wenham Robert M
Hospital of the University of Pennsylvania, Abramson Cancer Center, West Pavilion, Philadelphia, PA.
Virginia Commonwealth University Health, Massey Cancer Center, Richmond, VA.
J Clin Oncol. 2023 Jan 10;41(2):276-284. doi: 10.1200/JCO.22.00291. Epub 2022 Sep 7.
The adjunctive use of intraoperative molecular imaging (IMI) is gaining acceptance as a potential means to improve outcomes for surgical resection of targetable tumors. This confirmatory study examined the use of pafolacianine for real-time detection of folate receptor-positive ovarian cancer.
This phase III, open-label, 11-center study included subjects with known or suspected ovarian cancer, scheduled to undergo cytoreductive surgery. The objectives were to confirm safety and efficacy of pafolacianine (0.025 mg/kg IV), given ≥ 1 hour before intraoperative near-infrared imaging to detect macroscopic lesions not detected by palpation and normal white light.
From March 2018 through April 2020, 150 patients received a single infusion of pafolacianine (safety analysis set); 109 patients with folate receptor-positive ovarian cancer comprised the full analysis set for efficacy. In 33.0% of patients (95% CI, 24.3 to 42.7; < .001), pafolacianine with near-infrared imaging identified additional cancer on tissue not planned for resection and not detected by white light assessment and palpation, exceeding the prespecified threshold of 10%. Among patients who underwent interval debulking surgery, the rate was 39.7% (95% CI, 27.0 to 53.4; < .001). The sensitivity to detect ovarian cancer was 83%, and the patient false-positive rate was 24.8%. Investigators reported achieving complete R0 resection in 62.4% (68 of 109) of patients. Drug-related adverse events were reported by 30% of patients (45 of 150) and most commonly included nausea, vomiting, and abdominal pain. No drug-related serious adverse events or deaths were reported.
This phase III study of pafolacianine met its primary efficacy end point, identifying additional cancers not otherwise identified or planned for resection. Pafolacianine may offer an important real-time adjunct to current surgical approaches for ovarian cancer.
术中分子成像(IMI)的辅助应用作为一种改善可靶向肿瘤手术切除效果的潜在手段正逐渐得到认可。这项验证性研究探讨了帕氟拉西坦用于实时检测叶酸受体阳性卵巢癌的情况。
这项III期、开放标签、多中心研究纳入了已知或疑似卵巢癌且计划接受细胞减灭术的患者。目的是确认在术中近红外成像前≥1小时静脉注射帕氟拉西坦(0.025 mg/kg)的安全性和有效性,以检测触诊和普通白光未发现的宏观病变。
从2018年3月至2020年4月,150例患者接受了单次帕氟拉西坦输注(安全性分析集);109例叶酸受体阳性卵巢癌患者构成了疗效的完整分析集。在33.0%的患者中(95%置信区间,24.3至42.7;P<0.001),帕氟拉西坦联合近红外成像在未计划切除且白光评估和触诊未发现的组织上发现了额外的癌症,超过了预先设定的10%的阈值。在接受间隔性减瘤手术的患者中,这一比例为39.7%(95%置信区间,27.0至53.4;P<0.001)。检测卵巢癌的敏感性为83%,患者假阳性率为24.8%。研究人员报告称,62.4%(109例中的68例)的患者实现了R0完全切除。30%的患者(150例中的45例)报告了与药物相关的不良事件,最常见的包括恶心、呕吐和腹痛。未报告与药物相关的严重不良事件或死亡。
这项关于帕氟拉西坦的III期研究达到了其主要疗效终点,发现了未被其他方法发现或计划切除的额外癌症。帕氟拉西坦可能为当前卵巢癌手术方法提供重要的实时辅助手段。