TABLE 1.
No. | Authors and Year | Country | Tumor type | HPV ctDNA quantification | Cases No. in time‐to‐event analysis | Surrogate endpoint assessment (pre‐post‐treatment marker) | Medical treatment for outcome measurement |
---|---|---|---|---|---|---|---|
1 | Leung et al. (2021) 31 | Canada | LACC | HPV‐seq | 16 | PFS: EOT detectable HPV ctDNA | CRT |
2 | Jeannot et al. (2021) 18 | France | CC | ddPCR | 40 | PFS: EOT detectable HPV ctDNA | CRT, Neo‐chemotherapy |
PFS: Baseline detectable HPV ctDNA | |||||||
3 | Cabel et al. (2021) 32 | France | LACC | ddPCR | 14 | DFS: EOT detectable HPV ctDNA | CRT |
4 | Lefèvre et al. (2021) 33 | Denmark | SCCA | ddPCR | 45 | DFS: Baseline high and low pHPV | CRT |
5 | Tanaka et al. (2020) 34 | Japan | HNSCC | ddPCR | 35 | EFS: EOT detectable HPV ctDNA 16 | Radiotherapy with or without chemotherapy |
6 | Chera et al. (2020) 35 | USA | OPSCC | ddPCR | 115 | RFS: EOT detectable HPV ctDNA | CRT |
7 | Chera et al. (2019) 36 | USA | OPSCC | ddPCR | 48 | RDFS a : Baseline favorable and unfavorable clearance HPV ctDNA16 | CRT |
8 | Bernard‐Tessier et al. (2018) 37 | France | SCCA | ddPCR | 36 | PFS: EOT detectable HPV ctDNA | Chemotherapy |
9 | Cabel et al. (2018) 38 | France | ASCC [locally advanced] | ddPCR | 18 | DFS: EOT detectable HPV ctDNA | CRT |
10 | Dahlstrom et al. (2015) 26 | USA | OPSCC [OPC] | qPCR | 99 | PFS: Baseline detectable circulating HPV DNA | Chemotherapy and Radiotherapy b |
11 | Han et al. (2018) 39 | Canada | LACC | ddPCR | 19 | PFS: EOT detectable HPV ctDNA | CRT |
12 | Routman et al. (2022) 40 | USA | OPSCC | ddPCR | 159 | RFS: EOT detectable HPV ctDNA | Adjuvant radiation therapy |
13 | Sivars et al. (2022) 41 | Sweden | LACC | ddPCR | 18 | PFS: EOT detectable HPV ctDNA | CRT and EBRT |
Abbreviations: CC: cervical cancer; CRT: chemoradiotherapy; DFS: disease‐free survival; EBRT: external beam radiation therapy; EFS, event‐free survival; HNSCC: squamous cell carcinoma of the head and neck; LACC: locally advanced cervical cancer; OPSCC: oropharyngeal squamous cell carcinoma; PFS: progression‐free survival; RDFS: regional disease‐free survival; RFS: recurrence‐free survival; SCCA: Squamous cell carcinoma of the anus; SCCA: squamous cell carcinomas of the anal canal [Anal squamous cell carcinoma (SCCA)].
RDFS: was measured from the first CRT dose and defined as the time to detect or develop persistent or recurrent disease in the cervical lymph nodes.
During and after treatment, patients underwent regular clinical and radiologic examinations with a team of specialists in head and neck cancer, including surgeons, radiation oncologists, and medical oncologists.