Chriqui Louis-Emmanuel, Abdelnour-Berchtold Etienne, Zanfrini Edoardo, Devesa-Perez Severine, Gonzalez Michel, Krueger Thorsten, Ellefsen Kim, Destaillats Alice, Bonnet David, Hübner Martin, Bouchaab Hasna, Bassani-Sternberg Michal, Peters Solange, Cavin Sabrina, Perentes Jean Y
Division of Thoracic Surgery, University Hospital of Lausanne, Rue du Bugnon 46 1011, Lausanne, Switzerland.
Sponsor Research Office (SRO, University Hospital of Lausanne, Rue du Bugnon 46 1011, Lausanne, Switzerland.
Cancer Treat Res Commun. 2024;42:100858. doi: 10.1016/j.ctarc.2024.100858. Epub 2024 Dec 17.
Pleural carcinosis originates from various cancers. Its management consists in systemic therapies combined to dyspnea relief procedures. Prior studies have tested hyperthermic intrathoracic chemotherapy to treat pleural carcinosis with interesting patient survival results. However, these approaches were limited by local toxicity. Pre-clinical data have shown that hyperthermia combined to local pleural chemotherapy increased the immune response against tumors. Recently, pressurized intraperitoneal aerosol chemotherapies (PIPAC) showed improved cytostatic penetration in abdominal carcinosis with a 10-fold-lower chemotherapy dose and minimal side-effects. This approach was also tested in limited numbers of patients with pleural carcinosis but never combined with hyperthermia.
Pressurized IntraThoracic Hyperthermic Aerosol Cisplatin (PITHAC) is an open-label dose-escalation phase I trial. Patients with pleural carcinosis, eligible for the surgical management of their pleural effusion can be enrolled. Cisplatin (7.5-12-5-35-70 mg/m2) heated at 39±1 °C is delivered into the thoracic cavity before the surgical effusion management. Initially, the study consists in a dose escalation of the four different cisplatin doses. The primary endpoint is the maximal tolerated dose of cisplatin administered by PITHAC. The secondary and translational endpoints are adverse events and the immune response directed against cancer following PITHAC. There is then an expansion phase at the recommended cisplatin dose on an additional 15 patients with identical outcomes.
Pressurized intrathoracic delivery of chemotherapy under hyperthermic conditions was never tested so far. We plan to determine the safety of such an approach in patients managed for pleural carcinosis. If proven safe, PITHAC could be combined with systemic immunotherapies for the management of cancer.
ClinicalTrials.gov Identifier: NCT06281860.
胸膜癌转移起源于多种癌症。其治疗包括全身治疗联合缓解呼吸困难的程序。先前的研究已测试过胸腔内热化疗治疗胸膜癌转移,患者生存结果令人关注。然而,这些方法受到局部毒性的限制。临床前数据表明,热疗联合局部胸膜化疗可增强针对肿瘤的免疫反应。最近,加压腹腔内气溶胶化疗(PIPAC)显示在腹腔癌转移中细胞毒性药物的渗透有所改善,化疗剂量降低了10倍,且副作用最小。该方法也在少数胸膜癌转移患者中进行了测试,但从未与热疗联合使用。
加压胸腔内热气溶胶顺铂(PITHAC)是一项开放标签的剂量递增I期试验。符合胸腔积液手术治疗条件的胸膜癌转移患者可入组。在进行胸腔积液手术治疗前,将加热至39±1°C的顺铂(7.5 - 12 - 5 - 35 - 70 mg/m²)注入胸腔。最初,该研究包括对四种不同顺铂剂量进行剂量递增。主要终点是PITHAC给药的顺铂最大耐受剂量。次要终点和转化终点是不良事件以及PITHAC后针对癌症的免疫反应。然后在推荐的顺铂剂量下对另外15例具有相同结果的患者进行扩展阶段研究。
迄今为止,从未测试过热疗条件下胸腔内加压给药化疗的方法。我们计划确定这种方法在胸膜癌转移患者治疗中的安全性。如果证明安全,PITHAC可与全身免疫疗法联合用于癌症治疗。
ClinicalTrials.gov标识符:NCT06281860。