Novel Survivorship Paradigms in Head/Neck Cancer DOI
Maria Armache,

Alexis Larson,

Rachel Stemme

и другие.

Seminars in Radiation Oncology, Год журнала: 2025, Номер 35(2), С. 285 - 300

Опубликована: Март 14, 2025

Язык: Английский

Post-treatment surveillance imaging in head and neck cancer: a systematic review DOI Creative Commons
Stefaan Van Hoe, Robert Hermans

Insights into Imaging, Год журнала: 2024, Номер 15(1)

Опубликована: Фев. 5, 2024

Abstract Background In patients treated for head and neck cancer, imaging studies are usually obtained within 3–6 months after treatment assessment of response. After 6 months, most guidelines advocate clinical follow-up, with reserved clinically suspect or equivocal findings. However, some do recommend systematic surveillance, many clinicians tend to include type in their follow-up schemes. Objectives This review focuses on the usefulness routine (systematic) post-treatment surveillance cancer beyond first 3–6-month baseline study. Methods A literature search was conducted using PubMed Google Scholar. Additional were identified by reviewing reference lists. Only original papers considered. Results compared symptom-directed and/or finding-directed imaging. Five hundred twenty-one records through database search, 44 additional other sources. Forty-eight articles selected final review. Analysis these showed that almost half cases locoregional recurrences metastases only detected (40.9%), mean time detection recurrent metastatic disease (11.5 months) well period scan. Most authors reported superior results PET-CT when techniques. Conclusion Strong arguments found favor advanced during at least one preferably 2 years treatment. Critical relevance statement suggests may currently be underused cancer. Key points • long-term 521 revealed allowed initial more than 40% patients. Imaging Graphical

Язык: Английский

Процитировано

6

The Promise of Circulating Tumor DNA in Head and Neck Cancer DOI Open Access

Sukhkaran S. Aulakh,

Dustin A. Silverman, Kurtis Young

и другие.

Cancers, Год журнала: 2022, Номер 14(12), С. 2968 - 2968

Опубликована: Июнь 16, 2022

As the seventh most common cancer globally, head and neck cancers (HNC) exert considerable disease burden, with an estimated 277,597 deaths worldwide in 2020 alone. Traditional risk factors for HNC include tobacco, alcohol, betel nut; more recently, human papillomavirus has emerged as a distinct driver of disease. Currently, limitations screening surveillance methods often lead to identifying advanced stages, associated poor outcomes. Liquid biopsies, particular circulating tumor DNA (ctDNA), offer potential enhancing screening, early diagnosis, patients, improvements patient In this review, we examine current methodologies detecting ctDNA highlight research illustrating viral non-viral biomarker utilities treatment response, prognosis. We also summarize challenges future directions testing patients.

Язык: Английский

Процитировано

23

Multimodal detection of molecular residual disease in high-risk locally advanced squamous cell carcinoma of the head and neck DOI Creative Commons
Enrique Sanz‐García, Jinfeng Zou, Lisa Avery

и другие.

Cell Death and Differentiation, Год журнала: 2024, Номер 31(4), С. 460 - 468

Опубликована: Фев. 26, 2024

Abstract Up to 30% of patients with locally advanced head and neck squamous cell carcinoma (LA-HNSCC) relapse. Molecular residual disease (MRD) detection using multiple assays after definitive therapy has not been reported. In this study, we included LA-HNSCC (stage III Human Papilloma virus (HPV)-positive, III-IVB HPV-negative) treated curative intent. Plasma was collected pre-treatment, at 4–6 weeks (FU1) 8-12 (FU2) post-treatment. Circulating tumor DNA (ctDNA) analyzed a tumor-informed (RaDaR®) tumor-naïve (CAPP-seq) assay. HPV measured HPV-sequencing (HPV-seq) digital PCR (dPCR). A total 86 plasma samples from 32 were analyzed; all least 1 follow-up sample. Most stage HPV-positive (50%) received chemoradiation (78%). No had radiological FU2. With median 25 months, there 7 clinical relapses. ctDNA baseline detected in 15/17 (88%) by RaDaR associated recurrence free survival (RFS). Two relapsed within year showed MRD FU2 RaDaR; during shorter RFS ( p < 0.001). CAPP-seq pre-treatment = 0.09). HPV-seq or dPCR Sensitivity specificity for 40% 100% versus 20 90.5% CAPP-seq. 91.7% 50% dPCR. conclusion, can be before therapy. The assay but may detect who relapse year. more sensitive than detection.

Язык: Английский

Процитировано

5

Preoperative Circulating Tumor HPV DNA and Oropharyngeal Squamous Cell Disease DOI
Doreen Lam, Neel R. Sangal, Ashna Aggarwal

и другие.

JAMA Otolaryngology–Head & Neck Surgery, Год журнала: 2024, Номер 150(5), С. 444 - 444

Опубликована: Апрель 4, 2024

Importance The utility of preoperative circulating tumor tissue-modified viral human papillomavirus DNA (TTMV-HPV DNA) levels in predicting (HPV)–associated oropharyngeal squamous cell carcinoma (HPV+ OPSCC) disease burden is unknown. Objective To determine if HPV (ctHPVDNA) associated with patients HPV+ OPSCC who have undergone transoral robotic surgery (TORS). Design, Setting, and Participants This cross-sectional study comprised underwent primary TORS between September 2021 April 2023 at one tertiary academic institution. Patients treatment-naive (p16-positive) ctHPVDNA were included, those neck mass excision before collection excluded. Main Outcomes Measures main outcome was the association increasing size lymph node involvement surgical pathology. secondary adverse pathology, which included lymphovascular invasion, perineural or extranodal extension. Results A total 70 (65 men [93%]; mean [SD] age, 61 [8] years). Baseline ranged from 0 fragments/milliliter plasma (frag/mL) to 49 452 frag/mL (median [IQR], 272 [30-811] frag/mL). Overall, 58 (83%) had positive results for ctHPVDNA, 1 (1.4%) indeterminate results, 11 (15.6%) negative results. sensitivity detectable identifying pathology-confirmed 84%. Twenty-seven (39%) pathologic (pT) staging pT0 pT1, 34 (49%) pT2 staging, 9 (13%) pT3 pT4 staging. No clinically meaningful difference undetectable cohorts found Although median appeared be higher through stages pN1 pN2 stages, effect sizes small (pT stage: η2, 0.002 [95% CI, −1.188 0.827]; pN 0.043 −0.188 2.600]). Median log(TTMV-HPV active smokers (8.79 3.55-5.76]), compared never (5.92 −0.97 1.81]) former (4.99 0.92-6.23]). Regression analysis did not show an dimension metastatic deposit DNA). After univariate analysis, no Conclusions Relevance In this study, TORS.

Язык: Английский

Процитировано

5

Oligometastatic Head and Neck Cancer: Challenges and Perspectives DOI Open Access
Houda Bahig, Shao Hui Huang, Brian O’Sullivan

и другие.

Cancers, Год журнала: 2022, Номер 14(16), С. 3894 - 3894

Опубликована: Авг. 11, 2022

A minority of patients with metastatic head and neck squamous cell carcinoma (HNSCC) present oligometastatic disease. Oligometastasis not only reflects a disease state, but might also an opportunity for cure in the setting. Radical ablation all sites may confer prolonged survival possibly achieve some patients. However, substantial debate remains about whether could benefit from curative intent therapy or aggressive treatments expose to futile toxicity. Optimal selection patients, carefully balancing currently known prognostic factors against risks toxicity is critical. Emerging evidence suggests that limited burden disease, viral-related pharyngeal cancer, metachronous metastasis lung-only most this approach. Efforts are underway identify biomarkers can detect oligometastasis better select who would derive maximum radical The combination radiotherapy immunotherapy promises enhance anti-tumoral immune response help overcome resistance. optimization management algorithms, including patient selection, radiation dose sequencing, will be critical upcoming clinical trials. This review summarizes recent knowledge characteristics investigational efforts regarding HNSCC.

Язык: Английский

Процитировано

21

Circulating HPV DNA in HPV-associated cancers DOI
Guigao Lin, Jinming Li

Clinica Chimica Acta, Год журнала: 2023, Номер 542, С. 117269 - 117269

Опубликована: Фев. 24, 2023

Язык: Английский

Процитировано

11

Biomarkers of pembrolizumab efficacy in advanced anal squamous cell carcinoma: analysis of a phase II clinical trial and a cohort of long-term responders DOI Creative Commons
Brandon M. Huffman, Harshabad Singh, Lestat R. Ali

и другие.

Journal for ImmunoTherapy of Cancer, Год журнала: 2024, Номер 12(1), С. e008436 - e008436

Опубликована: Янв. 1, 2024

Recent trials suggest that programmed cell death 1 (PD-1)-directed immunotherapy may be beneficial for some patients with anal squamous carcinoma and biomarkers predictive of response are greatly needed. This multicenter phase II clinical trial (NCT02919969) enrolled metastatic or locally advanced incurable (n=32). Patients received pembrolizumab 200 mg every 3 weeks. The primary endpoint the was objective rate (ORR). Exploratory objectives included analysis potential including assessment tumor-associated immune populations multichannel immunofluorescence circulating tumor tissue modified viral-human papillomavirus DNA (TTMV-HPV DNA) using serially collected blood samples. To characterize features long-term responders, we combined data from our prospective a retrospective cohort cancer treated anti-PD-1 (n=18). In study, ORR to monotherapy 9.4% median progression-free survival 2.2 months. Despite high level HPV positivity observed TTMV-HPV testing, majority had low levels CD8+PD-1+ T cells on pretreatment biopsy. who benefited decreasing scores complete responder's became undetectable. Long-term responses were in one patient (5.3 years) three (2.5, 6, 8 cohort. responders HPV-positive tumors, lacked liver metastases, achieved radiological response. Pembrolizumab has durable efficacy rare subset cancers. However, despite persistence infection, indicated by DNA, most cancers have numbers resistant pembrolizumab.

Язык: Английский

Процитировано

4

Evaluating human papillomavirus testing, prevalence, and association with prognosis in head and neck squamous cell carcinoma by subsite: A national cancer database study DOI
Joshua Barlow, Shivee Gilja, Rocco Ferrandino

и другие.

American Journal of Otolaryngology, Год журнала: 2024, Номер 45(3), С. 104243 - 104243

Опубликована: Фев. 28, 2024

Язык: Английский

Процитировано

4

Utility of TTMV-HPV DNA in resolving indeterminate findings during oropharyngeal cancer surveillance DOI
Scott A. Roof, James Jabalee, Eleni M. Rettig

и другие.

Oral Oncology, Год журнала: 2024, Номер 155, С. 106874 - 106874

Опубликована: Июнь 14, 2024

Язык: Английский

Процитировано

4

Evaluating Tumor Tissue Modified Viral (TTMV)-HPV DNA for the Early Detection of Anal Squamous Cell Carcinoma Recurrence DOI Open Access
Rafi Kabarriti, Shane Lloyd, James Jabalee

и другие.

Cancers, Год журнала: 2025, Номер 17(2), С. 174 - 174

Опубликована: Янв. 8, 2025

The incidence and mortality of anal squamous cell carcinoma (ASCC) are rising, with greater than 80% cases linked to human papillomavirus (HPV), primarily HPV16. Post-treatment surveillance can be challenging due the limitations anoscopy, digital rectal exam (DARE), imaging. Plasma tumor tissue modified viral (TTMV)-HPV DNA has shown strong sensitivity, specificity, predictive value in detecting recurrence HPV-driven oropharyngeal cancer. Here, we investigate ability TTMV-HPV for early detection ASCC. This retrospective clinical case series included 117 patients ASCC across 7 U.S. centers, monitored during routine care between March 2020 June 2024. Physician-reported data biomarker testing were combined create a comprehensive, longitudinal dataset evaluating test performance metrics. Patients had median age 63 years post-diagnosis follow-up 19 months. HPV status was confirmed by (52%) or p16 immunohistochemistry (39%). Of those tested pretreatment, 85% positive result. clearance within three months post-treatment associated significantly better recurrence-free survival. per-patient (PPV), negative (NPV) 82.8%, 98.4%, 96.0%, 92.5%. 24 documented test, first evidence 14 (58.3%), lead time 59 days (range: 10-536). accurately resolved 94.3% indeterminate findings. provides sensitive specific approach recurrent resolving

Язык: Английский

Процитировано

0