HPV ctDNA detection of high-risk HPV types during chemoradiotherapy for locally advanced cervical cancer

被引:38
|
作者
Cabel, L. [1 ,2 ]
Bonneau, C. [3 ,4 ]
Bernard-Tessier, A. [5 ,6 ]
Hequet, D. [4 ,7 ]
Tran-Perennou, C. [5 ,6 ]
Bataillon, G. [5 ,6 ]
Rouzier, R. [4 ,7 ]
Feron, J-G [4 ]
Fourchotte, V [4 ]
Le Brun, J-F [8 ]
Benoit, C. [9 ]
Rodrigues, M. [1 ,2 ]
Scher, N. [10 ,11 ]
Minsat, M. [10 ,11 ]
Legrier, M-E [12 ,13 ]
Bieche, I [5 ,6 ,14 ]
Proudhon, C. [15 ]
Sastre-Garau, X. [16 ]
Bidard, F-C [1 ,2 ,3 ,15 ]
Jeannot, E. [5 ,6 ]
机构
[1] Inst Curie, Dept Med Oncol, Paris, France
[2] Inst Curie, Dept Med Oncol, St Cloud, France
[3] Paris Saclay Univ, UVSQ, Gif Sur Yvette, France
[4] Inst Curie, Dept Surg Oncol, St Cloud, France
[5] Inst Curie, Dept Pathol & Genet, 26 Rue Ulm, Paris, France
[6] Inst Curie, Dept Pathol & Genet, St Cloud, France
[7] Paris Saclay Univ, U900, UVSQ, Gif Sur Yvette, France
[8] CCC Francois Baclesse, Dept Gynecol & Obstet, Caen, France
[9] Ctr Jean Perrin, Dept Radiat Oncol, Clermont Ferrand, France
[10] Inst Curie, Dept Radiat Oncol, Paris, France
[11] Inst Curie, Dept Radiat Oncol, St Cloud, France
[12] Inst Curie, Dept Res, Paris, France
[13] Inst Curie, Dept Res, St Cloud, France
[14] Paris Univ, Paris, France
[15] Inst Curie, Circulating Tumor Biomarkers Lab, Paris, France
[16] Hop Intercommunal Creteil, Dept Pathol, Creteil, France
关键词
circulating tumor DNA; human papillomavirus; cervical cancer; chemoradiotherapy; prognostic marker; CIRCULATING TUMOR DNA; HUMAN-PAPILLOMAVIRUS DNA; CELL-CARCINOMA ANTIGEN; CONCURRENT CHEMORADIOTHERAPY; CLASSIFICATION; PLASMA;
D O I
10.1016/j.esmoop.2021.100154
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Chemoradiotherapy (CRT) is the standard of care for patients diagnosed with locally advanced cervical cancer (LACC), a human papillomavirus (HPV)-related cancer that relapses in 30%-60% of patients. This study aimed to (i) design HPV droplet digital PCR (ddPCR) assays for blood detection (including rare genotypes) and (ii) monitor blood HPV circulating tumor DNA (HPV ctDNA) levels during CRT in patients with LACC. Methods: We analyzed blood and tumor samples from 55 patients with HPV-positive LACC treated by CRT in a retrospective cohort (n = 41) and a prospective cohort (n = 14). HPV-ctDNA detection was carried out by genotype-specific ddPCR. Results: HPV ctDNA was successfully detected in 69% of patients (n = 38/55) before CRT for LACC, including nine patients with a rare genotype. HPV-ctDNA level was correlated with HPV copy number in the tumor (r = 0.41, P < 0.001). HPV-ctDNA positivity for HPV18 (20%, n = 2/10) was significantly lower than for HPV16 (77%, n 27/35) or other types (90%, n 9/10, P = 0.002). HPV-ctDNA detection (positive versus negative) before CRT was associated with tumor stage (P = 0.037) and lymph node status (P = 0.02). Taking into account all samples from the end of CRT and during follow-up in the prospective cohort, positive HPV-ctDNA detection was associated with lower disease-free survival (DFS) (P = 0.048) and overall survival (OS) (P = 0.0013). Conclusion: This is one of the largest studies to report HPV-ctDNA detection before CRT and showed clearance of HPV ctDNA at the end of treatment in most patients. Residual HPV ctDNA at the end of CRT or during follow-up could help to identify patients more likely to experience subsequent relapse.
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页数:8
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