Sarkaria Inderpal S, Biro Timothy G, Singhal Sunil, Reddy Rishindra M, Martin Linda W, Rice David C, Lopez Alex S, Stevens Gary, Barret Tina, Murthy Sudish C
UT Southwestern Medical Center, Dallas, TX.
On Target Laboratories, West Lafayette, IN.
Clin Lung Cancer. 2025 Mar;26(2):104-115. doi: 10.1016/j.cllc.2024.11.004. Epub 2024 Nov 16.
With increased early detection efforts, surgery for early-stage lung cancer is expected to rise. Pafolacianine is the first FDA approved targeted optical imaging agent indicated as an adjunct for intraoperative identification of malignant and nonmalignant pulmonary lesions in adult patients with known or suspected cancer in the lung.
This is a retrospective review of the malignant and nonmalignant lesions identified by pafolacianine with intraoperative molecular imaging (IMI) in the multi-center Phase 2 and Phase 3 ELUCIDATE clinical trials. All lesions meeting the intent to treat criteria from the combined studies were included. Histopathology for malignant and nonmalignant lesions and immunohistochemistry (ICH) for folate receptor alpha (FRα) and folate receptor beta (FRβ), which pafolacianine binds to, were assessed.
A total of 273 lesions resected from 191 patients were analyzed. The identification of primary and occult malignant lesions with pafolacianine in combination with standard practice was improved (P < .001) when compared to standard practice alone. A range of histologies were demonstrated including adenocarcinoma (primary and metastatic), squamous cell carcinoma, adenoid cystic carcinoma, chordoma, lymphoma, and papillary thyroid cancer. Ninety-two percent (205 of 223) of lesions tested for folate expression were positive for FRα or FRβ expression.
While initially intended to identify adenocarcinoma, IMI with pafolacianine targets a broad histological cross-section of malignant and nonmalignant primary and metastatic lesions in the lung. As real-world use expands, additional insight will continue to inform utility of pafolacianine in clinical practice and may broaden clinical applicability.
随着早期检测力度的加大,早期肺癌手术量预计会上升。帕福拉新是首个获美国食品药品监督管理局(FDA)批准的靶向光学成像剂,被用作辅助手段,用于在已知或疑似患有肺癌的成年患者中术中识别恶性和非恶性肺部病变。
这是一项回顾性研究,对多中心2期和3期ELUCIDATE临床试验中通过帕福拉新与术中分子成像(IMI)识别的恶性和非恶性病变进行分析。纳入了所有符合联合研究中治疗意向标准的病变。对恶性和非恶性病变进行组织病理学检查,并对帕福拉新所结合的叶酸受体α(FRα)和叶酸受体β(FRβ)进行免疫组织化学(ICH)评估。
共分析了191例患者切除的273个病变。与单独的标准做法相比,帕福拉新联合标准做法对原发性和隐匿性恶性病变的识别有所改善(P <.001)。病变组织学类型多样,包括腺癌(原发性和转移性)、鳞状细胞癌、腺样囊性癌、脊索瘤、淋巴瘤和甲状腺乳头状癌。检测叶酸表达的病变中有92%(223个中的205个)FRα或FRβ表达呈阳性。
虽然帕福拉新最初旨在识别腺癌,但与帕福拉新的IMI可针对肺部恶性和非恶性原发性及转移性病变的广泛组织学类型。随着其在现实世界中的应用不断扩大,更多的见解将继续为帕福拉新在临床实践中的效用提供信息,并可能拓宽其临床应用范围。