Silihe Kamga Kevine, Fiering Steven
Department of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Hanover, NH, United States.
Front Immunol. 2025 Jun 18;16:1545000. doi: 10.3389/fimmu.2025.1545000. eCollection 2025.
Cancer immunotherapy has made astonishing progress in the last 10-15 years, and the rate of progress is accelerating. However, only 20 to 40% of patients benefit from this therapy with most immunotherapy applied post discovery of metastatic disease when therapeutic impact is more difficult to achieve. The first line of treatment for many patients following diagnosis is surgery. Neoadjuvant immunotherapy, i.e. administration of immune therapy prior to surgery, has the potential to improve overall survival rates. Many patients without detectable metastases are diagnosed with a high risk of future metastasis and could benefit from effective neoadjuvant immunotherapy. An ideal neoadjuvant immune therapy will stimulate immune response against the identified tumor as well as undetected metastasis and be safe with minimal adverse events. In addition, the antitumor immune response it generates should not be blocked by subsequent surgery and should not delay the normal timeline of surgery. Finally, it should be relatively inexpensive. These features describe intratumoral immunotherapy (ITIT), a therapeutic approach that directly administers immune stimulatory agents or treatments into the tumor. By delivering the therapy directly into the tumor, it enhances local drug concentration while minimizing nonspecific immune activation and adverse events associated with systemic immunotherapy. ITIT can generate effective local immune response against tumor antigens, which expands the pool of tumor-recognizing effector T cells. ITIT induces and activates tumor specific T cell within days after the treatment, so surgery is not delayed. Tumor-recognizing effector T cells generated locally attack cancer both locally and systemically, targeting metastasis through the "abscopal effect". Neoadjuvant ITIT options are extensive and expanding and need research into optimal options to combine and associated dosing and timing. With the needed effort, neoadjuvant ITIT will develop into a safe, rapid and effective addition to current cancer therapies.
在过去10至15年中,癌症免疫疗法取得了惊人进展,且进展速度正在加快。然而,只有20%至40%的患者能从这种疗法中获益,因为大多数免疫疗法是在发现转移性疾病后应用的,此时治疗效果更难实现。对许多患者而言,诊断后的一线治疗方法是手术。新辅助免疫疗法,即在手术前给予免疫治疗,有可能提高总体生存率。许多未检测到转移的患者被诊断为未来转移风险高,可能受益于有效的新辅助免疫疗法。理想的新辅助免疫疗法将刺激针对已识别肿瘤以及未检测到的转移灶的免疫反应,并且安全,不良事件最少。此外,它所产生的抗肿瘤免疫反应不应被后续手术阻断,也不应延迟手术的正常时间安排。最后,它应该相对便宜。这些特点描述了瘤内免疫疗法(ITIT),一种将免疫刺激剂或治疗直接注入肿瘤的治疗方法。通过将治疗直接输送到肿瘤中,它提高了局部药物浓度,同时将与全身免疫疗法相关的非特异性免疫激活和不良事件降至最低。ITIT可以产生针对肿瘤抗原的有效局部免疫反应,从而扩大识别肿瘤的效应T细胞库。ITIT在治疗后数天内诱导并激活肿瘤特异性T细胞,因此不会延迟手术。局部产生的识别肿瘤的效应T细胞在局部和全身攻击癌症,通过“远隔效应”靶向转移灶。新辅助ITIT的选择广泛且不断增加,需要研究最佳的联合选择以及相关的给药方式和时间。通过所需的努力,新辅助ITIT将发展成为当前癌症治疗中一种安全、快速且有效的补充方法。