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Record W4414923280 · doi:10.3389/fonc.2025.1657282

The effect of tislelizumab on complete and pathological complete response in non-small cell lung cancer: a systematic review and meta-analysis

2025· review· en· W4414923280 on OpenAlexaboutno aff
Feng Qian, Yan Xiaoxia, Liping Gao, Hui Li, Hongying Jiang

Bibliographic record

VenueFrontiers in Oncology · 2025
Typereview
Languageen
FieldMedicine
TopicCancer Immunotherapy and Biomarkers
Canadian institutionsnot available
FundersLanzhou University
KeywordsChemotherapyPathologicalComplete responseLungLung cancerCell

Abstract

fetched live from OpenAlex

Background Immune checkpoint inhibitors have transformed non-small cell lung cancer (NSCLC) treatment, and while overall survival (OS) and progression-free survival (PFS) are well-established, a comprehensive meta-analysis focusing on complete response (CR) and pathological complete response (pCR) with tislelizumab-based therapies in NSCLC is lacking. Methods This systematic review and meta-analysis was conducted following PRISMA guidelines. A thorough literature search was performed across PubMed, Embase, and Web of Science. We included both randomized controlled trials and observational studies of tislelizumab in NSCLC, focusing on extracting data for radiological complete response (CR, based on RECIST 1.1 criteria) and pathological complete response (pCR, defined as absence of residual invasive cancer in resected surgical specimens). Risk of bias was assessed using the Cochrane Collaboration’s tool and the Newcastle-Ottawa Scale. Statistical analyses were performed using the ‘meta’ package in R. 95% confidence intervals (CIs) and odds ratios (ORs) were calculated for CR and pCR, and subgroup analyses were conducted. Results 7 studies were enrolled in the meta-analysis. The results on pCR showed significant heterogeneity (I2 = 92.5%), with a random effects OR of 2.1103 (95% CI: 0.5195 to 8.5727). Subgroup analysis for pCR by disease type revealed a statistically significant difference between NSCLC and SCC only subgroups under the common effect model (p < 0.001). Furthermore, the pCR subgroup analysis by comparator drug showed a statistically significant difference (p < 0.0001) between Pembrolizumab+Chemotherapy (OR 0.6968, 95% CI: 0.3803 to 1.2767) and Chemotherapy alone (OR 7.3123, 95% CI: 2.9204 to 18.3092). For CR, the meta-analysis demonstrated minimal heterogeneity (I2 = 0.0%), yielding a significant random effects OR of 2.6277 (95% CI: 1.2858 to 5.3699). Subgroup analysis for CR comparing tislelizumab plus chemotherapy to chemotherapy alone showed a significant advantage (OR 3.8690, 95% CI: 1.5423 to 9.7059). Conclusion Tislelizumab combined with chemotherapy significantly improves CR rates in NSCLC compared to chemotherapy alone. While pCR data exhibit high heterogeneity, the findings highlight tislelizumab’s role in achieving deep tumor responses.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.015
metaresearch head score (Gemma)0.029
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Meta-analysis · Consensus signal: Meta-analysis
GenreCandidate signal: Review · Consensus signal: Review
Teacher disagreement score0.021
Threshold uncertainty score0.077

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0150.029
Meta-epidemiology (narrow)0.0030.001
Meta-epidemiology (broad)0.0210.046
Bibliometrics0.0060.007
Science and technology studies0.0010.001
Scholarly communication0.0030.002
Open science0.0020.001
Research integrity0.0030.002
Insufficient payload (model declined to judge)0.0030.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.040
GPT teacher head0.366
Teacher spread0.326 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designMeta-analysis
Domainnot available
GenreReview

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations1
Published2025
Admission routes1
Has abstractyes

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