Evidence map›Paper›PMID 42052476›Full record

ArticleFrontiers in oncology2026

The role of AI-driven decision support in immunotherapy for predicting pathological complete response in triple-negative breast cancer.

Di Lu, Xihui Tu, Yaling Zeng, Huixi Zhong, Tengfei Xing, Yuying Wang, Rui Wang, Purong Zhang

Abstract read
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.

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0citing papers in PubMed
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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

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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

8 authors.

Di LuSchool of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Xihui TuCollege of Clinical Medicine, North Sichuan Medical College, Nanchong, Sichuan, China.
Yaling ZengSchool of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Huixi ZhongSchool of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Tengfei XingDepartment of Breast, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Yuying WangDepartment of Health Management Center, Qionglai Medical Center Hospital, Qionlai, Sichuan, China.
Rui WangSichuan Mianyang 404 Hospital, Mianyang, Sichuan, China.
Purong ZhangDepartment of Breast, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Neoadjuvant pembrolizumab combined with chemotherapy has become a standard treatment strategy for early-stage triple-negative breast cancer (TNBC). However, real-world evidence regarding its effectiveness and models for predicting pathological complete response (pCR) remain limited. Methods: We retrospectively collected data from 248 patients with TNBC who received neoadjuvant chemotherapy (NACT) with or without pembrolizumab followed by surgery between May 2023 and December 2025. Patients were categorized into two groups: the pembrolizumab-chemotherapy group (n = 40) and the chemotherapy-alone group (n = 208). Propensity score matching (PSM) was applied to balance baseline characteristics. Machine learning models were developed using routinely available clinical and pathological variables to predict pCR, and model interpretability was evaluated using SHapley Additive exPlanations (SHAP). Results: Both before and after PSM, the pembrolizumab-chemotherapy group achieved a higher pCR rate than the chemotherapy-alone group (before: 50.0% vs. 30.8%, p = 0.030; after: 47.2% vs. 26.5%, p = 0.037). LASSO regression selected six variables associated with pCR, including pembrolizumab, age, sum of diameters of target lesions (SLD), Ki67, N stage, and clinical stage. In the training cohort, these six variables were used to develop eight machine learning models to predict pCR. In the validation cohort, the MLP model achieved the highest receiver operating characteristic-area under the curve (ROC-AUC) of 0.71. The calibration curve and decision curve analysis (DCA) further indicated good calibration and clinical utility of the MLP model. Conclusions: Neoadjuvant pembrolizumab combined with chemotherapy further improved pCR rates in TNBC, and the MLP-based model demonstrated good performance for predicting pCR.

Indexed as

immunotherapymachine learningneoadjuvant chemotherapypathological complete responsepembrolizumabtriple-negative breast cancer

Identifiers

PMID42052476
PMCPMC13111214

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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.