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pmid:35498426

Identification and Validation of a Prognostic Prediction Model in Diffuse Large B-Cell Lymphoma.

Jiaqin Yan · Wei Yuan · Junhui Zhang · Ling Li · Lei Zhang · Xudong Zhang · Mingzhi Zhang

Frontiers in endocrinology · 2022 doi:10.3389/fendo.2022.846357

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title
Identification and Validation of a Prognostic Prediction Model in Diffuse Large B-Cell Lymphoma.
doi
10.3389/fendo.2022.846357
pmid
35498426
authors array · 7 items
[0]
Jiaqin Yan
[1]
Wei Yuan
[2]
Junhui Zhang
[3]
Ling Li
[4]
Lei Zhang
[5]
Xudong Zhang
[6]
Mingzhi Zhang
journal
Frontiers in endocrinology
year
2022
abstract
Background: Diffuse large B-cell lymphoma (DLBCL) is a heterogeneous group with varied pathophysiological, genetic, and clinical features, accounting for approximately one-third of all lymphoma cases worldwide. Notwithstanding that unprecedented scientific progress has been achieved over the years, the survival of DLBCL patients remains low, emphasizing the need to develop novel prognostic biomarkers for early risk stratification and treatment optimization. Method: In this study, we screened genes related to the overall survival (OS) of DLBCL patients in datasets GSE117556, GSE10846, and GSE31312 using univariate Cox analysis. Survival-related genes among the three datasets were screened according to the criteria: hazard ratio (HR) >1 or <1 and p-value <0.01. Least Absolute Shrinkage and Selection Operator (LASSO) and multivariate Cox regression analysis were used to optimize and establish the final gene risk prediction model. The TCGA-NCICCR datasets and our clinical cohort were used to validate the performance of the prediction model. CIBERSORT and ssGSEA algorithms were used to estimate immune scores in the high- and low-risk groups. Results: We constructed an eight-gene prognostic signature that could reliably predict the clinical outcome in training, testing, and validation cohorts. Our prognostic signature also performed distinguished areas under the ROC curve in each dataset, respectively. After stratification based on clinical characteristics such as cell-of-origin (COO), age, eastern cooperative oncology group (ECOG) performance status, international prognostic index (IPI), stage, and MYC/BCL2 expression, the difference in OS between the high- and low-risk groups was statistically significant. Next, univariate and multivariate analyses revealed that the risk score model had a significant prediction value. Finally, a nomogram was established to visualize the prediction model. Of note, we found that the low-risk group was enriched with immune cells. Conclusion: In summary, we identified an eight-gene prognostic prediction model that can effectively predict survival outcomes of patients with DLBCL and built a nomogram to visualize the perdition model. We also explored immune alterations between high- and low-risk groups.
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Multivariate Cox regression analysis showed that the risk score model was an independent prognostic factor for poor prognosis (p < 0.0001, HR = 1.380) ( Figure 6B ).
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sections[14] "Validation of the Performance of Our Prediction Model" paragraph 2
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Multivariate Cox regression analysis showed that the risk score model was an independent prognostic factor for poor prognosis (p < 0.0001, HR = 1.380) ( Figure 6B ).
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The datasets GSE117556, GSE10846 and GSE31312 for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo).The datasets NCICCR for this study can be found at TCGA (https://portal.gdc.cancer.gov/repository).
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sections[17] "Data Availability Statement" paragraph 2
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The datasets GSE117556, GSE10846 and GSE31312 for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo).The datasets NCICCR for this study can be found at TCGA (https://portal.gdc.cancer.gov/repository).
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Compared with other indicators, the risk score was superior for predicting the patient prognosis (AUC = 0.820) ( Figure 6C ).
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Compared with other indicators, the risk score was superior for predicting the patient prognosis (AUC = 0.820) ( Figure 6C ).
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sections[14] "Validation of the Performance of Our Prediction Model" paragraph 2
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Compared with other indicators, the risk score was superior for predicting the patient prognosis (AUC = 0.820) ( Figure 6C ).
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Compared with other indicators, the risk score was superior for predicting the patient prognosis (AUC = 0.820) ( Figure 6C ).
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Prediction of survival in diffuse large B cell lymphoma treated with chemotherapy plus Rituximab
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GSM3302936
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[686]
GSM3303616
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GSM3303867
sample_count
928
group_sizes
null
group_sizes_basis
null
platform
14951
taxon
Homo sapiens
title
Molecular definition of high grade B cell lymphoma: a centroblast-like group with potential for more effective therapy
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[3] object · 15 fields
id
data:geo:GSE31312
role
raw
format
geo-series
media_type
application/vnd.ncbi.geo-series+json
uri
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE31312
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE31312
version
null
note
The datasets GSE117556, GSE10846 and GSE31312 for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo).The datasets NCICCR for this study can be found at TCGA (https://portal.gdc.cancer.gov/repository).
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The datasets GSE117556, GSE10846 and GSE31312 for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo).The datasets NCICCR for this study can be found at TCGA (https://portal.gdc.cancer.gov/repository).
access_statement_kind
data_availability_statement
sample_accessions array · 498 items
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[244]
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[245]
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[256]
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[266]
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[267]
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[293]
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[294]
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[303]
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[304]
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[305]
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[308]
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[309]
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[313]
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[314]
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[315]
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[414]
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Development and application of a new immunophenotypic algorithm for molecular subtype classification of Diffuse Large B-Cell Lymphoma (DLBCL): Report from an International DLBCL Rituximab-CHOP Consortium Program Study
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Multivariate Cox regression analysis showed that the risk score model was an independent prognostic factor for poor prognosis (p < 0.0001, HR = 1.380) ( Figure 6B ).
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Multivariate Cox regression analysis showed that the risk score model was an independent prognostic factor for poor prognosis (p < 0.0001, HR = 1.380) ( Figure 6B ).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35498426", "kind": "science-record", "revision": 4, "content_hash": "sha256:0235ebf492f5064ba31830c69a25a7ba045bad334446b41b82b1249cca10530c", "created_at": "2026-11-01T18:14:23Z", "updated_at": "2026-11-01T22:06:26Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification and Validation of a Prognostic Prediction Model in Diffuse Large B-Cell Lymphoma.", "doi": "10.3389/fendo.2022.846357", "pmid": "35498426", "authors": ["Jiaqin Yan", "Wei Yuan", "Junhui Zhang", "Ling Li", "Lei Zhang", "Xudong Zhang", "Mingzhi Zhang"], "journal": "Frontiers in endocrinology", "year": 2022, "abstract": "Background: Diffuse large B-cell lymphoma (DLBCL) is a heterogeneous group with varied pathophysiological, genetic, and clinical features, accounting for approximately one-third of all lymphoma cases worldwide. Notwithstanding that unprecedented scientific progress has been achieved over the years, the survival of DLBCL patients remains low, emphasizing the need to develop novel prognostic biomarkers for early risk stratification and treatment optimization.\nMethod: In this study, we screened genes related to the overall survival (OS) of DLBCL patients in datasets GSE117556, GSE10846, and GSE31312 using univariate Cox analysis. Survival-related genes among the three datasets were screened according to the criteria: hazard ratio (HR) >1 or <1 and p-value <0.01. Least Absolute Shrinkage and Selection Operator (LASSO) and multivariate Cox regression analysis were used to optimize and establish the final gene risk prediction model. The TCGA-NCICCR datasets and our clinical cohort were used to validate the performance of the prediction model. CIBERSORT and ssGSEA algorithms were used to estimate immune scores in the high- and low-risk groups.\nResults: We constructed an eight-gene prognostic signature that could reliably predict the clinical outcome in training, testing, and validation cohorts. Our prognostic signature also performed distinguished areas under the ROC curve in each dataset, respectively. After stratification based on clinical characteristics such as cell-of-origin (COO), age, eastern cooperative oncology group (ECOG) performance status, international prognostic index (IPI), stage, and MYC/BCL2 expression, the difference in OS between the high- and low-risk groups was statistically significant. Next, univariate and multivariate analyses revealed that the risk score model had a significant prediction value. Finally, a nomogram was established to visualize the prediction model. Of note, we found that the low-risk group was enriched with immune cells.\nConclusion: In summary, we identified an eight-gene prognostic prediction model that can effectively predict survival outcomes of patients with DLBCL and built a nomogram to visualize the perdition model. We also explored immune alterations between high- and low-risk groups.", "claims": [{"id": "claim-method", "statement": "Multivariate Cox regression analysis showed that the risk score model was an independent prognostic factor for poor prognosis (p < 0.0001, HR = 1.380) ( Figure 6B ).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35498426", "locator": "sections[14] \"Validation of the Performance of Our Prediction Model\" paragraph 2", "quote": "Multivariate Cox regression analysis showed that the risk score model was an independent prognostic factor for poor prognosis (p < 0.0001, HR = 1.380) ( Figure 6B )."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets GSE117556, GSE10846 and GSE31312 for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo).The datasets NCICCR for this study can be found at TCGA (https://portal.gdc.cancer.gov/repository).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35498426", "locator": "sections[17] \"Data Availability Statement\" paragraph 2", "quote": "The datasets GSE117556, GSE10846 and GSE31312 for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo).The datasets NCICCR for this study can be found at TCGA (https://portal.gdc.cancer.gov/repository)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Compared with other indicators, the risk score was superior for predicting the patient prognosis (AUC = 0.820) ( Figure 6C ).", "kind": "quantitative", "target": {"value": 0.82, "unit": "auc", "tolerance": null, "source": "Compared with other indicators, the risk score was superior for predicting the patient prognosis (AUC = 0.820) ( Figure 6C )."}, "evidence": [{"asset": "source:pmid:35498426", "locator": "sections[14] \"Validation of the Performance of Our Prediction Model\" paragraph 2", "quote": "Compared with other indicators, the risk score was superior for predicting the patient prognosis (AUC = 0.820) ( Figure 6C )."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Compared with other indicators, the risk score was superior for predicting the patient prognosis (AUC = 0.820) ( Figure 6C ).", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:35498426"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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"GSM361244"], "sample_count": 420, "group_sizes": null, "group_sizes_basis": null, "platform": "570", "taxon": "Homo sapiens", "title": "Prediction of survival in diffuse large B cell lymphoma treated with chemotherapy plus Rituximab", "resolution_checked_at": "2026-11-01T15:39:54Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}, {"id": "data:geo:GSE117556", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE117556", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE117556", "version": null, "note": "The datasets GSE117556, GSE10846 and GSE31312 for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo).The datasets NCICCR for this study can be found at TCGA (https://portal.gdc.cancer.gov/repository).", 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"asset:data:geo:GSE117556 not downloaded", "asset:data:geo:GSE117556 licence not read", "asset:data:geo:GSE31312 not downloaded", "asset:data:geo:GSE31312 licence not read"]}, "analysis": {"state": "complete", "methods": [{"id": "method-1", "family": "survival_analysis", "specific": "cox_proportional_hazards", "label": "Survival analysis", "dsl_operations": ["cox_ph"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 1.0, "band": "verbatim", "quote": "Multivariate Cox regression analysis showed that the risk score model was an independent prognostic factor for poor prognosis (p < 0.0001, HR = 1.380) ( Figure 6B )."}}, {"id": "method-2", "family": "survival_analysis", "specific": "kaplan_meier", "label": "Survival analysis", "dsl_operations": ["survival_km"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 0.8, "band": "high", "quote": "Kaplan-Meier"}}, {"id": "method-3", "family": "survival_analysis", "specific": "log_rank_test", "label": "Survival analysis", "dsl_operations": ["logrank_test"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 0.8, "band": "high", "quote": "log-rank"}}, {"id": "method-4", "family": "network_analysis", "specific": "pathway_enrichment", "label": "Network / pathway analysis", "dsl_operations": ["pathway_enrich"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["edge_list"], "evidence": {"score": 0.8, "band": "high", "quote": "GO enrichment"}}, {"id": "method-5", "family": "diagnostic_evaluation", "specific": "roc", "label": "Diagnostic test evaluation", "dsl_operations": ["confusion_counts", "roc_curve", "sensitivity_specificity", "solve_confusion_matrix", "classification_metrics", "published_precision_envelope"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["reference_standard_and_test"], "evidence": {"score": 0.7, "band": "medium", "quote": "ROC curve"}}], "targets": [{"id": "target-published-estimate", "claim_id": "claim-target-result", "operation": "classification_metrics", "expected_value": 0.82, "unit": "auc", "tolerance": null, "state": "complete", "note": "The published estimate as the reader quoted it from the paper. No tolerance is published because the paper states none."}], "gaps": []}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "complete", "tier": "R1", "blocking_axis": "none", "blocked_on": "nothing:replicable_now", "axes": {"method": {"tier": "R1", "expressible": true, "required_operations": ["cox_ph"], "missing_operations": [], "basis": "The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards."}, "capability": {"tier": "R1", "capability_id": "capability:computational_analysis", "availability_state": "owned", "basis": "The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE117556", "GSE10846", "GSE31312"], "resolved_accessions": ["GSE117556", "GSE10846", "GSE31312"], "statements": ["The datasets GSE117556, GSE10846 and GSE31312 for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo).The datasets NCICCR for this study can be found at TCGA (https://portal.gdc.cancer.gov/repository)."], "basis": "The paper names GSE117556, GSE10846, GSE31312 in GEO and the accession resolves in the repository. No dataset was downloaded and no licence was read."}}, "can_run": {"dsl_operations": ["cox_ph"], "assets": ["source:pmid:35498426", "data:geo:GSE10846"], "steps": ["run_analysis"]}, "must_build": {"dsl_operations": [], "converters": [], "readers": [], "capabilities": [], "data_gaps": ["data:geo:GSE10846"]}, "gaps": []}, "review": {"state": "partial", "machine_critique": {"kind": "extraction_review", "reader": {"model": "MiniMax-M3.1-Flash", "provider": "minimax", "provider_family": "minimax", "read_at": "2026-11-01T17:44:27Z", "independence": "single_reader"}, "evidence_check": {"method": "verbatim", "availability": "verbatim"}, "calls": 5, "usage": {"prompt_tokens": 8781, "completion_tokens": 2084, "cached_tokens": 256}}, "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:35498426", "type": "paper", "label": "pmid:35498426"}, {"id": "source:pmid:35498426", "type": "manuscript", "label": "PMID 35498426 full text"}, {"id": "data:geo:GSE10846", "type": "dataset", "label": "GEO GSE10846"}], "activities": [{"id": "activity-reading-sci-2026-11-01", "type": "classification", "used": [{"id": "pmid:35498426", "type": "paper", "label": "pmid:35498426"}, {"id": "source:pmid:35498426", "type": "manuscript", "label": "PMID 35498426 full text"}, {"id": "data:geo:GSE10846", "type": "dataset", "label": "GEO GSE10846"}], "agent": "agent:corpus-assay-engine"}, {"id": "activity-read-35498426", "type": "extraction", "used": ["source:pmid:35498426"], "agent": "agent:minimax-reader"}, {"id": "activity-resolve-GSE10846", "type": "accession_resolution", "used": ["data:geo:GSE10846"], "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:35498426", "parent_hash": "sha256:d89c425d40674f976fb4fbce12acc58f610667a9fcb1a9849230ea4127fe4816", "fork_of": null, "generation": 3}, "gaps": ["asset:data:geo:GSE10846 licence not read", "asset:data:geo:GSE10846 not downloaded", "asset:data:geo:GSE117556 licence not read", "asset:data:geo:GSE117556 not downloaded", "asset:data:geo:GSE31312 licence not read", "asset:data:geo:GSE31312 not downloaded", "execution.not_run", "review.human_critique", "review.independent_reader", "review.machine_critique"], "assays": [{"role": "analysis", "definition_id": "survival_analysis", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["cox_ph"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["Multivariate Cox regression analysis showed that the risk score model was an independent prognostic factor for poor prognosis (p < 0.0001, HR = 1.380) ( Figure 6B )."], "order_basis": "analysis_only", "id": "assay:1"}]}