ReviewFrontiers in oncology2025
Research advances in evaluation methods for neoadjuvant therapy of tumors.
Review in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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.
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.
Who cites it
3 citing papers in PubMed.
- The combination of cyclin D1 and MRI radiomics parameters improves breast cancer diagnosis and NACT efficacy assessment.Journal of medical biochemistry · 2026Article
- Circulating tumor DNA dynamics predict pathological response and guide therapy personalization in the neoadjuvant setting.Discover oncology · 2026Review
- Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Preoperative neoadjuvant therapy is crucial for large malignant tumors or tumors that are challenging to resect. Consequently, an objective assessment of its therapeutic efficacy is important. Currently, the conventional evaluation methods for neoadjuvant therapy of tumors are mainly divided into two categories: imaging-based and pathological evaluations. In imaging-based evaluation, the World Health Organization criteria are straightforward; however, they exhibit some issues such as unclear criteria for minimum lesions and measurement errors. Moreover, although the Response Evaluation Criteria In Solid Tumors criteria have been improved, they remain insensitive to internal tumor changes and are prone to measurement errors. The Modified Response Evaluation Criteria In Solid Tumors criteria are specifically designed for hepatocellular carcinoma, yet they have limitations, such as difficulty defining complex tumor boundaries. The Positron Emission Tomography Response Criteria in Solid Tumors criteria, which integrate positron emission tomography/computed tomography, offer high accuracy but are influenced by factors related to the patient's body condition and equipment. The Choi criteria, which comprehensively consider tumor size and density, can be used to evaluate the efficacy of targeted therapy; however, they are characterized by cumbersome measurement procedures and strong subjectivity. In terms of pathological evaluation, the Huvos score determines the therapeutic effect based on the degree of tumor necrosis, which can guide subsequent treatment and prognosis. However, the evaluation time is fixed and subject to interference from pathological procedures. The Miller-Payne criteria focus on changes in the number and density of tumor cells and provide a reference for surgical decision-making. Nevertheless, it does not consider lymph node metastasis. The Residual Cancer Burden assessment criteria comprehensively quantify residual tumors by integrating multiple factors. Moreover, these offer a precise assessment of breast cancer and have a high value in predicting prognosis. However, their parameter calculation is complex and highly subjective. In summary, each method has its own advantages and disadvantages. With the advancement of scientific research, evaluation methods for neoadjuvant therapy are constantly evolving. In-depth research into these methods can help identify more accurate and effective evaluation strategies, providing a more scientific basis for tumor treatment and propelling the field of tumor therapy toward greater precision.
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Registered trials
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.