Dr Mary and Ron Neal Cancer Center, Houston Methodist Hospital, Houston, Texas.
Houston Methodist Research Institute, Houston, Texas.
Int J Radiat Oncol Biol Phys. 2024 Apr 1;118(5):1531-1540. doi: 10.1016/j.ijrobp.2023.08.044. Epub 2023 Aug 24.
A phase 2 study of stereotactic body radiation therapy (SBRT) and in situ oncolytic virus therapy in metastatic non-small cell lung cancer (mNSCLC) followed by pembrolizumab (STOMP) was designed to explore the dual approach in enhancing single pembrolizumab with ADV/HSV-tk plus valacyclovir gene therapy and SBRT in mNSCLC.
STOMP is a single-arm, open-label phase 2 study. Patients with mNSCLC received intratumoral injections of ADV/HSV-tk (5 × 10 vp) and SBRT (30 Gy in 5 fractions) followed by pembrolizumab 200 mg IV every 3 weeks until disease progression or intolerable toxicity. The primary endpoint was overall response rate (ORR) (complete response [CR] and partial response [PR]). Secondary endpoints included clinical benefit rate (CBR) (CR, PR and stable disease [SD]), progression-free survival (PFS), overall survival (OS), and safety.
28 patients were enrolled, of whom 27 were evaluated for response. The ORR was 33.3%, including 2 CR (7.4%) and 7 PR (25.9%). CBR was 70.4%. Six of eight (75.0%) patients who were immune checkpoint inhibitor (ICI) refractory derived clinical benefits. Responders had durable responses with median PFS, and OS not reached. The entire cohort had a median PFS of 7.4 months (95% CI, 5.1-9.6 months), and median OS of 18.1 months (95% CI, 15.4-20.9 months). The combination was well tolerated, with grade 3 or higher toxicity in 6 (21.4%) patients.
The dual approach of in situ ADV/HSV-tk plus valacyclovir gene therapy and SBRT as a chemotherapy-sparing strategy to enhance the antitumor effect of pembrolizumab is a well-tolerated encouraging treatment in patients with mNSCLC.
立体定向体部放射治疗(SBRT)和原位溶瘤病毒治疗转移性非小细胞肺癌(mNSCLC)后序贯派姆单抗(STOMP)的 2 期研究旨在探索通过 ADV/HSV-tk 加伐昔洛韦基因治疗和 SBRT 增强单药派姆单抗在 mNSCLC 中的双重作用。
STOMP 是一项单臂、开放标签的 2 期研究。mNSCLC 患者接受瘤内注射 ADV/HSV-tk(5×10 vp)和 SBRT(30 Gy 分 5 次),然后序贯派姆单抗 200 mg IV,每 3 周一次,直至疾病进展或不可耐受的毒性。主要终点是总缓解率(ORR)(完全缓解[CR]和部分缓解[PR])。次要终点包括临床获益率(CBR)(CR、PR 和稳定疾病[SD])、无进展生存期(PFS)、总生存期(OS)和安全性。
共入组 28 例患者,其中 27 例可评估疗效。ORR 为 33.3%,包括 2 例 CR(7.4%)和 7 例 PR(25.9%)。CBR 为 70.4%。8 例免疫检查点抑制剂(ICI)耐药患者中有 6 例(75.0%)获得临床获益。缓解者的 PFS 和 OS 均未达到,具有持久的缓解。全队列的中位 PFS 为 7.4 个月(95%CI,5.1-9.6 个月),中位 OS 为 18.1 个月(95%CI,15.4-20.9 个月)。该联合方案耐受性良好,6 例(21.4%)患者发生 3 级或以上毒性。
原位 ADV/HSV-tk 加伐昔洛韦基因治疗和 SBRT 作为一种化疗节约策略,增强派姆单抗的抗肿瘤作用,在 mNSCLC 患者中是一种耐受性良好、令人鼓舞的治疗方法。