Evidence map›Paper›PMID 41971451›Full record

ArticleFrontiers in oncology2026

Neoadjuvant ctDNA-MRD monitoring uncovers occult progression despite radiologic response in locally advanced hypopharyngeal carcinoma: a case report.

Zhaoyang Wang, Lin Gui, Ye Zhang, Shengkai Huang, Shun Wang, Xiwei Zhang, Fa Zhang, Xiaotong Yan, Zongmin Zhang, Shaoyan Liu and 1 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Zhaoyang WangDepartment of Head and Neck Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Lin GuiDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Ye ZhangDepartment of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Shengkai HuangDepartment of Clinical Laboratory, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Shun WangDepartment of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Xiwei ZhangDepartment of Head and Neck Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Fa ZhangDepartment of Head and Neck Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Xiaotong YanDepartment of Head and Neck Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Zongmin ZhangDepartment of Head and Neck Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Shaoyan LiuDepartment of Head and Neck Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Changming AnDepartment of Head and Neck Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The assessment of treatment response during neoadjuvant therapy for head and neck squamous cell carcinoma (HNSCC) relies largely on radiographic and endoscopic evaluations, which may fail to detect minimal residual disease (MRD). Circulating tumor DNA (ctDNA)-based MRD monitoring has emerged as a sensitive biomarker capable of revealing molecular disease activity that is not captured by imaging. Evidence supporting its use in the neoadjuvant setting of HNSCC remains limited. Case presentation: We report a 53-year-old man with locally advanced hypopharyngeal squamous cell carcinoma (cT4N2cM0) who received three cycles of neoadjuvant immunochemotherapy (toripalimab, cisplatin, and nab-paclitaxel). Radiologic and endoscopic assessment demonstrated a partial response with a 71.6% reduction in tumor burden and near-complete mucosal normalization. In contrast, ctDNA-MRD analysis showed elevated ctDNA levels compared with baseline, indicating molecular progression. Despite the favorable imaging response, the patient developed new distant metastases three months after definitive chemoradiotherapy and maintenance immunotherapy, confirming systemic disease progression. Discussion: This case highlights the limitations of imaging in differentiating true tumor regression from residual disease during neoadjuvant therapy. Persistent ctDNA-MRD despite radiologic remission may signal occult progression and could influence critical treatment decisions, including the choice between surgery, chemoradiation, or systemic intensification. Accumulating evidence from other tumor types suggests that MRD clearance may predict pathological complete response (pCR), raising the possibility that accurate molecular assessment could help identify patients who may safely avoid surgery. However, MRD applications in neoadjuvant HNSCC-particularly hypopharyngeal carcinoma-remain sparsely studied. Conclusion: ctDNA-MRD may provide complementary and potentially earlier insights into treatment response compared with imaging alone. Its incorporation into neoadjuvant strategies for HNSCC warrants further investigation and may ultimately support more personalized and accurate therapeutic decision-making.

Indexed as

CtDNAhypopharyngeal carcinomaimmunochemotherapyMRDneoadjuvant therapytreatment response

Identifiers

PMID41971451
PMCPMC13065681

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.