TY - JOUR
T1 - A Phase 2 Study of In Situ Oncolytic Virus Therapy and Stereotactic Body Radiation Therapy Followed by Pembrolizumab in Metastatic Non-Small Cell Lung Cancer
AU - Guan, Jian
AU - Sun, Kai
AU - Guerrero, Carlo A.
AU - Zheng, Junjun
AU - Xu, Yitian
AU - Mathur, Sunil
AU - Teh, Bin S.
AU - Farach, Andrew
AU - Zhang, Jun
AU - Butler, Edward
AU - Pan, Ping Ying
AU - Zsigmond, Eva
AU - Mei, Zhuyong
AU - Mejia, Jaime
AU - Chen, Shu Hsia
AU - Chang, Jenny C.
AU - Bernicker, Eric H.
N1 - Funding Information:
This research was supported by Merck Sharp and Dohme Corp.
Funding Information:
Disclosures: E.H.B. received support from Merck. J.C.C. discloses the following support unrelated to this study: grant from the National Institute of Health, Cancer Prevention & Re Inst of Texas and Department of Defense; consulting fees from Clinical Oncology Study Section, Breast Cancer Research Foundation annual meeting, 2022 Cancer Stem Cell Conference, Astra Zeneca American Society of Clinical Oncology Destiny Advisory Board, LOXO Lilly Advisory Board, Triple negative Breast Cancer advisory board, Lily Virtual Advisory board and Astra Zeneca/Merck Advisory Board.
Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2023/8/24
Y1 - 2023/8/24
N2 - Purpose: 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. Methods and Materials: STOMP is a single-arm, open-label phase 2 study. Patients with mNSCLC received intratumoral injections of ADV/HSV-tk (5 × 1011 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. Results: 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. Conclusions: 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.
AB - Purpose: 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. Methods and Materials: STOMP is a single-arm, open-label phase 2 study. Patients with mNSCLC received intratumoral injections of ADV/HSV-tk (5 × 1011 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. Results: 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. Conclusions: 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.
UR - http://www.scopus.com/inward/record.url?scp=85173107250&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85173107250&partnerID=8YFLogxK
U2 - 10.1016/j.ijrobp.2023.08.044
DO - 10.1016/j.ijrobp.2023.08.044
M3 - Article
C2 - 37625523
AN - SCOPUS:85173107250
SN - 0360-3016
VL - 118
SP - 1531
EP - 1540
JO - International Journal of Radiation Oncology Biology Physics
JF - International Journal of Radiation Oncology Biology Physics
IS - 5
ER -