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pmid:35372049
Establish of an Initial Platinum-Resistance Predictor in High-Grade Serous Ovarian Cancer Patients Regardless of Homologous Recombination Deficiency Status.
Yongmei Li · Yufei Nie · Hongyan Guo · Hua Guo · Chunfang Ha · Yuan Li
Frontiers in oncology · 2022 doi:10.3389/fonc.2022.847085
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Complete file
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However, nearly 20%-30% of patients with OC are initial platinum resistant (IPR), and there is a lack of valid tools to predict whether they will be primary platinum resistant or not prior to chemotherapy.\nMethods: Transcriptome data from The Cancer Genome Atlas (TCGA) was downloaded as the training data, and transcriptome data of GSE15622, GSE102073, GSE19829, and GSE26712 were retrieved from Gene Expression Omnibus (GEO) as the validation cohorts. Differentially expressed genes (DEGs) were selected between platinum-sensitive and platinum-resistant patients from the training cohort, and multiple machine-learning algorithms [including random forest, XGboost, and least absolute shrinkage and selection operator (LASSO) regression] were utilized to determine the candidate genes from DEGs. Then, we applied logistic regression to establish the IPR signature based on the expression. Finally, comprehensive clinical, genomic, and survival feature were analyzed to understand the application value of the established IPR signature.\nResults: A total of 532 DEGs were identified between platinum-resistant and platinum-sensitive samples, and 11 of them were shared by these three-machine learning algorithms and utilized to construct an IPR prediction signature. The area under receiver operating characteristic curve (AUC) was 0.841 and 0.796 in the training and validation cohorts, respectively. Notably, the prediction capacity of this signature was stable and robust regardless of the patients' homologous recombination deficiency (HRD) and mutation burden status. Meanwhile, the genomic feature was concordant between samples with high- or low-IPR signature, except a significantly higher prevalence of gain at Chr19q.12 (regions including CCNE1) in the high-IPR signature samples. The efficacy of prediction of platinum resistance of IPR signature successfully transferred to the precise survival prediction, with the AUC of 0.71, 0.72, and 0.66 to predict 1-, 3-, and 5-year survival, respectively. At last, we found a significantly different tumor-infiltrated lymphocytes feature, including lower abundance of CD4+ naive T cells in the samples with high-IPR signature. A relatively lower tumor immune dysfunction and exclusion (TIDE) value and more sensitivity to multiple therapies including Gefitinib may suggest the potency to transfer from platinum-based therapy to immunotherapy or target therapies in patients with high-IPR signature.\nConclusion: Our study established an IPR signature based on the expression of 11 genes that could stably and robustly distinguish OC patients with IPR and/or poor outcomes, which may guide therapeutic regimes tailoring.", "claims": [{"id": "claim-method", "statement": "Next, by utilizing multivariate logistic regression analysis, an IPR prediction model was established, and the formula was as follow:", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35372049", "locator": "sections[13] \"Establishment of an IPR Signature\" paragraph 2", "quote": "Next, by utilizing multivariate logistic regression analysis, an IPR prediction model was established, and the formula was as follow:"}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/ Supplementary Material . 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The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE15622", "GSE102073", "GSE19829", "GSE26712"], "resolved_accessions": ["GSE15622", "GSE102073", "GSE19829", "GSE26712"], "statements": ["The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors."], "basis": "The paper names GSE15622, GSE102073, GSE19829, GSE26712 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read."}}, "can_run": {"dsl_operations": ["glm_logit_fit"], "assets": ["source:pmid:35372049", "data:geo:GSE102073"], "steps": ["run_analysis"]}, "must_build": {"dsl_operations": [], "converters": [], "readers": [], "capabilities": [], "data_gaps": ["data:geo:GSE102073"]}, "gaps": []}, "review": {"state": "partial", "machine_critique": {"kind": "extraction_review", "reader": {"model": "MiniMax-M3.1-Flash", "provider": "minimax", "provider_family": "minimax", "read_at": "2026-11-01T17:40:39Z", "independence": "single_reader"}, "evidence_check": {"method": "verbatim", "availability": "verbatim"}, "calls": 5, "usage": {"prompt_tokens": 14653, "completion_tokens": 1529, "cached_tokens": 128}}, "human_critique": null, "stages": [{"id": "extraction", "state": "complete", "reader": "MiniMax-M3.1-Flash", "provider": "minimax"}], "gaps": ["review.independent_reader", "review.machine_critique", "review.human_critique"]}, "execution": {"state": "absent", "status": "not_run", "mode": null, "runs": [], "gaps": ["execution.not_run"]}, "provenance": {"entities": [{"id": "pmid:35372049", "type": "paper", "label": "pmid:35372049"}, {"id": "source:pmid:35372049", "type": "manuscript", "label": "PMID 35372049 full text"}, {"id": "data:geo:GSE102073", "type": "dataset", "label": "GEO GSE102073"}], "activities": [{"id": "activity-reading-sci-2026-11-01", "type": "classification", "used": [{"id": "pmid:35372049", "type": "paper", "label": "pmid:35372049"}, {"id": "source:pmid:35372049", "type": "manuscript", "label": "PMID 35372049 full text"}, {"id": "data:geo:GSE102073", "type": "dataset", "label": "GEO GSE102073"}], "agent": "agent:corpus-assay-engine"}, {"id": "activity-read-35372049", "type": "extraction", "used": ["source:pmid:35372049"], "agent": "agent:minimax-reader"}, {"id": "activity-resolve-GSE102073", "type": "accession_resolution", "used": ["data:geo:GSE102073"], "agent": "agent:corpus-assay-engine"}], "agents": [{"id": "agent:corpus-assay-engine", "type": "software", "label": "Corpus assay engine"}, {"id": "agent:minimax-reader", "type": "software", "label": "MiniMax literature reader"}], "source_run_id": "reading-sci-2026-11-01", "dsl_catalogue_fingerprint": "343fb30756ba6ec3", "capability_table_fingerprint": "2cb3e42f047d2ecf", "snapshot_id": "ba34b49490d9bfaf"}, "lineage": {"parent_id": "pmid:35372049", "parent_hash": "sha256:7fb153834949a66a9a68db37a9220ad96b9c9f479f275c16b2a7d3c50ed7b1a0", "fork_of": null, "generation": 3}, "gaps": ["asset:data:geo:GSE102073 licence not read", "asset:data:geo:GSE102073 not downloaded", "asset:data:geo:GSE15622 licence not read", "asset:data:geo:GSE15622 not downloaded", "asset:data:geo:GSE19829 licence not read", "asset:data:geo:GSE19829 not downloaded", "asset:data:geo:GSE26712 licence not read", "asset:data:geo:GSE26712 not downloaded", "execution.not_run", "method.reader_differs_from_extractor", "review.human_critique", "review.independent_reader", "review.machine_critique"], "assays": [{"role": "analysis", "definition_id": "regression_modelling", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["glm_logit_fit"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["Next, by utilizing multivariate logistic regression analysis, an IPR prediction model was established, and the formula was as follow:"], "order_basis": "analysis_only", "id": "assay:1"}]}