Personalized Biomarker-Based Umbrella Trial for Patients With Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma: KCSG HN 15-16 TRIUMPH Trial

Author:

Keam Bhumsuk12ORCID,Hong Min Hee3ORCID,Shin Seong Hoon4,Heo Seong Gu56ORCID,Kim Ji Eun7ORCID,Ahn Hee Kyung8,Lee Yun-Gyoo9ORCID,Park Keon-Uk10ORCID,Yun Tak11,Lee Keun-Wook12ORCID,Kim Sung-Bae13ORCID,Lee Sang-Cheol14ORCID,Kim Min Kyoung15,Cho Sang Hee16ORCID,Oh So Yeon17ORCID,Park Sang-Gon18,Hwang Shinwon1920ORCID,Nam Byung-Ho21,Kim Sangwoo22ORCID,Kim Hye Ryun3ORCID,Yun Hwan Jung23ORCID,

Affiliation:

1. Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea

2. Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea

3. Divison of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea

4. Department of Internal Medicine, Kosin University Gospel Hospital, Busan, Republic of Korea

5. Yonsei Cancer Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea

6. Division of Cancer Data Science, National Cancer Center, Goyang, Republic of Korea

7. Department of Pathology, Seoul National University College of Medicine, SMG-SNU Boramae Hospital, Seoul, Republic of Korea

8. Division of Medical Oncology, Department of Internal Medicine, Gachon University Gil Medical Center, Incheon, Republic of Korea

9. Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea

10. Department of Internal Medicine, Keimyung University Dongsan Hospital, Daegu, Republic of Korea

11. Rare Cancers Clinic, Center for Specific Organs Cancer, National Cancer Center, Goyang, Republic of Korea

12. Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Republic of Korea

13. Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea

14. Division of Hematology-Oncology, Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, Republic of Korea

15. Division of Hematology-Oncology, Department of Internal Medicine, Yeungnam University Hospital, Yeungnam University College of Medicine, Daegu, Republic of Korea

16. Department of Hemato-Oncology, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, Gwangju, Republic of Korea

17. Department of Internal Medicine, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Republic of Korea

18. Department of Hemato-Oncology, Chosun University Hospital, Gwangju, Republic of Korea

19. Department of Biomedical Systems Informatics, Yonsei University College of Medicine, Seoul, Republic of Korea

20. Department of Medicine, Physician-Scientist Program, Yonsei University College of Medicine, Seoul, Republic of Korea

21. HERINGS, Seoul, Republic of Korea

22. Department of Biomedical Systems Informatics, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul, Republic of Korea

23. Division of Hemato-Oncology, Department of Internal Medicine, Chungnam National University Hospital, Daejeon, Republic of Korea

Abstract

PURPOSE A precise oncologic approach for head and neck squamous cell carcinoma (HNSCC) is necessary. We performed a genomic profile-based umbrella trial for the patients with platinum-refractory recurrent and/or metastatic HNSCC. METHODS In this multicenter, open-label, single-arm phase II trial, we performed targeted next-generation sequencing (NGS). Patients were assigned to each treatment arm on the basis of their matching genomic profiles: arm 1, alpelisib, a PIK3CA inhibitor; arm 2, poziotinib, an epidermal growth factor receptor/HER2 inhibitor; arm 3, nintedanib, an fibroblast growth factor receptor inhibitor; and arm 4, abemaciclinb, a CDK4/6 inhibitor. If there was no matching target, patients were allocated to arm 5, duvalumab ± tremelimumab, anti–PD-L1/cytotoxic T-cell lymphocyte-4 inhibitor. When progressive disease (PD) occurred in arms 1-4, cross over to arm 5 was allowed. The primary end point was disease control rate (DCR) in arm 1 and overall response rate (ORR) in arms 2-5 by investigator assessment. RESULTS Between October 2017 and August 2020, 203 patients were enrolled, including crossover. In arm 1, the ORR was 21.2% and DCR was 65.6%. The ORR was 0% for arm 2, 42.9% for arm 3, 0% for arm 4, and 15.6% for arm 5. In the case of PD with durvalumab, tremelimumab was added, and the ORR for durvalumab + tremelimumab was 2.2%. The median progression-free survival was 3.4, 3.2, 5.6, 1.6, and 1.7 months for each arm, respectively. The median overall survival was 12.4, 6.1, 11.1, 9.1, and 12.7 months, respectively. Overall, the toxicity profiles were manageable, and there were no treatment-related deaths. CONCLUSION To our knowledge, this study is the first biomarker-driven umbrella trial for platinum-refractory HNSCC using matched molecular targeted agents. We found that NGS-based genomic phenotyping was methodologically feasible and applicable.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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