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pmid:32457841

Immunoscore Predicts Survival in Early-Stage Lung Adenocarcinoma Patients.

Zihuan Zhao · Dan Zhao · Ji Xia · Yi Wang · Buhai Wang

Frontiers in oncology · 2020 doi:10.3389/fonc.2020.00691

Paper

complete

Experiment

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Data

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pmid:32457841
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title
Immunoscore Predicts Survival in Early-Stage Lung Adenocarcinoma Patients.
doi
10.3389/fonc.2020.00691
pmid
32457841
authors array · 5 items
[0]
Zihuan Zhao
[1]
Dan Zhao
[2]
Ji Xia
[3]
Yi Wang
[4]
Buhai Wang
journal
Frontiers in oncology
year
2020
abstract
Background: The lung cancer staging system is insufficient for a comprehensive evaluation of patient prognosis. We constructed a novel immunoscore model to predict patients with high risk and poor survival. Method: Immunoscore was developed based on z-score transformed enrichment score of 11 immune-related gene sets of 109 immune risk genes. The immunoscore model was trained in lung adenocarcinoma cohort from The Cancer Genome Atlas (TCGA-LUAD) (n = 400), and validated in other two independent cohorts from Gene Expression Omnibus (GEO), GSE31210 (n = 219) and GSE68465 (n = 356). Meta-set (n = 975) was formed by combining all training and testing sets. Result: High immunoscore conferred worse prognosis in all sets. It was an independent prognostic factors in multivariate Cox analysis in training, testing and meta-set [hazard ratio (HR) = 2.96 (2.24-3.9), P < 0.001 in training set; HR = 1.99 (1.21-3.26), P = 0.006 in testing set 1; HR = 1.48 (1.69-2.39), P = 0.005 in testing set 2; HR = 2.01 (1.69-2.39), P < 0.001 in meta-set]. Immunoscore-clinical prognostic signature (ICPS) was developed by integrating immunoscore and clinical characteristic, and had higher C-index than immunoscore or stage alone in all sets [0.72 (ICPS) vs. 0.7 (immunoscore) or 0.59 (stage) in training set; 0.75 vs. 0.72 or 0.7 in testing set 1; 0.65 vs. 0.61 or 0.62 in testing set 2; 0.7 vs. 0.66 or 0.64 in meta-set]. Genome analysis revealed that immunoscore was positively correlated with tumor mutation burden (R = 0.22, P < 0.001). Besides, high immunoscore was correlated with high proportion of carcinoma-associated fibroblasts (R = 0.32, P < 0.001) in tumor microenvironment but fewer CD8+ cells infiltration (R = -0.28, P < 0.001). Conclusion: The immunoscore and ICPS are potential biomarkers for evaluating patient survival. Further investigations are required to validate and improve their prediction accuracy.
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C-index of ICPS was compared with stage or immunoscore alone using “compareC” package (43).
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sections[8] "Immunoscore-Clinical Prognostic Signature Construction" paragraph 2
quote
C-index of ICPS was compared with stage or immunoscore alone using “compareC” package (43).
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Data Availability Statement Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov, https://www.ncbi.nlm.nih.gov/geo.
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sections[23] "Data Availability Statement" paragraphs 1-2
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Data Availability Statement Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov, https://www.ncbi.nlm.nih.gov/geo.
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Data Availability Statement Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov, https://www.ncbi.nlm.nih.gov/geo.
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Data Availability Statement Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov, https://www.ncbi.nlm.nih.gov/geo.
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Gene expression data for pathological stage I-II lung adenocarcinomas
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sample_count
462
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null
group_sizes_basis
null
platform
96
taxon
Homo sapiens
title
caArray_jacob-00182: Gene expression-based survival prediction in lung adenocarcinoma: a multi-site, blinded validation study
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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asset:table:pmid:32457841:1
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sha256:20e7afea0158551534bf88130dfdeb03bc231f7e9d1bda7ee8f1660dc7d67778
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open
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verified
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read_table
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identifier
section[14]/table-wrap[1]#T1
version
null
note
Detailed patient clinical characteristics.
structure object · 5 fields
pmcid
PMC7225293
section_index
14
section_title
Immunoscore Model Construction
row_count
27
column_count
4
table object · 8 fields
label
Table 1
caption
Detailed patient clinical characteristics.
rows array · 27 items
[0] array · 4 items
[0]
Characteristics
[1]
Training set
[2]
Testing set 1
[3]
Testing set 2
[1] array · 4 items
[0]
Source
[1]
TCGA
[2]
GSE31210
[3]
GSE68465
[2] array · 4 items
[0]
Sample size
[1]
400
[2]
219
[3]
356
[3] array · 4 items
[0]
Platform
[1]
RNA-seq
[2]
Affymetrix Human Genome U133 Plus 2.0 Array
[3]
Affymetrix Human Genome U133A Array
[4] array · 1 item
[0]
AJCC stage
[5] array · 4 items
[0]
IA
[1]
130 (32.5)
[2]
112 (51.1)
[3]
112 (31.5)
[6] array · 4 items
[0]
IB
[1]
143 (35.8)
[2]
53 (24.2)
[3]
155 (43.5)
[7] array · 4 items
[0]
II
[1]
—
[2]
54 (24.7)
[3]
—
[8] array · 4 items
[0]
IIA
[1]
57 (14.2)
[2]
—
[3]
24 (6.7)
[9] array · 4 items
[0]
IIB
[1]
70 (17.5)
[2]
—
[3]
65 (18.3)
[10] array · 1 item
[0]
Age group
[11] array · 4 items
[0]
≤ 65
[1]
190 (47.5)
[2]
170 (77.6)
[3]
186 (52.2)
[12] array · 4 items
[0]
> 65
[1]
201 (50.2)
[2]
49 (22.4)
[3]
170 (47.8)
[13] array · 1 item
[0]
Smoking history
[14] array · 4 items
[0]
Non-smoker
[1]
57 (14.2)
[2]
112 (51.1)
[3]
40 (11.2)
[15] array · 4 items
[0]
Ever-smoker
[1]
333 (83.2)
[2]
107 (48.9)
[3]
243 (68.3)
[16] array · 4 items
[0]
Unknown
[1]
10 (2.5)
[2]
—
[3]
73 (20.5)
[17] array · 1 item
[0]
Gender
[18] array · 4 items
[0]
Male
[1]
177 (45.6)
[2]
103 (46.4)
[3]
175 (49.2)
[19] array · 4 items
[0]
Female
[1]
211 (54.4)
[2]
119 (53.6)
[3]
181 (50.8)
[20] array · 1 item
[0]
Survival status
[21] array · 4 items
[0]
Alive
[1]
273 (68.2)
[2]
186 (84.9)
[3]
189 (53.1)
[22] array · 4 items
[0]
Dead
[1]
127 (31.8)
[2]
33 (15.1)
[3]
167 (46.9)
[23] array · 1 item
[0]
Genome alteration
[24] array · 4 items
[0]
≤ 0.2
[1]
170 (42.5)
[2]
—
[3]
—
[25] array · 4 items
[0]
> 0.2
[1]
229 (57.2)
[2]
—
[3]
—
[26] array · 4 items
[0]
Unknown
[1]
1 (0.2)
[2]
—
[3]
—
locator
section[14]/table-wrap[1]#T1
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[0]
asset:data:geo:GSE31210 not downloaded
[1]
asset:data:geo:GSE31210 licence not read
[2]
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[3]
asset:data:geo:GSE68465 licence not read
analysis object · 4 fields
state
partial
methods array · 3 items
[0] object · 10 fields
id
method-1
family
group_comparison
specific
anova
label
Group comparison
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[0]
group_summary
[1]
welch_t
[2]
bootstrap_mean_difference
[3]
group_comparison_anova
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
0.8
band
high
quote
ANOVA
[1] object · 10 fields
id
method-2
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survival_analysis
specific
kaplan_meier
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Survival analysis
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[0]
survival_km
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
0.8
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high
quote
Kaplan-Meier
[2] object · 10 fields
id
method-3
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null
specific
null
label
C-index
dsl_operations array · 0 items
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
score
1
band
verbatim
quote
C-index of ICPS was compared with stage or immunoscore alone using “compareC” package (43).
targets array · 0 items
gaps array · 1 item
[0]
method.reader_named_unmapped
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
true
required_operations array · 4 items
[0]
group_summary
[1]
welch_t
[2]
bootstrap_mean_difference
[3]
group_comparison_anova
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: anova.
capability object · 4 fields
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 object · 6 fields
tier
R1
reachable
true
accessions array · 2 items
[0]
GSE31210
[1]
GSE68465
resolved_accessions array · 2 items
[0]
GSE31210
[1]
GSE68465
statements array · 1 item
[0]
Data Availability Statement Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov, https://www.ncbi.nlm.nih.gov/geo.
basis
The paper names GSE31210, GSE68465 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 4 items
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group_summary
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welch_t
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bootstrap_mean_difference
[3]
group_comparison_anova
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source:pmid:32457841
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asset:table:pmid:32457841:1
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[0]
run_analysis
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data_gaps array · 1 item
[0]
data:geo:GSE31210
gaps array · 0 items
review object · 5 fields
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partial
machine_critique object · 5 fields
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extraction_review
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
2026-10-31T18:20:03Z
independence
single_reader
evidence_check object · 2 fields
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verbatim
availability
verbatim
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3
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42500
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2235
cached_tokens
784
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id
extraction
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complete
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MiniMax-M3.1-Flash
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minimax
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review.independent_reader
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review.machine_critique
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review.human_critique
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absent
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execution.not_run
provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:32457841
type
paper
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pmid:32457841
[1] object · 3 fields
id
source:pmid:32457841
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manuscript
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PMID 32457841 full text
[2] object · 3 fields
id
data:geo:GSE31210
type
dataset
label
GEO GSE31210
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
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pmid:32457841
type
paper
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pmid:32457841
[1] object · 3 fields
id
source:pmid:32457841
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manuscript
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PMID 32457841 full text
[2] object · 3 fields
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data:geo:GSE31210
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dataset
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GEO GSE31210
agent
agent:corpus-assay-engine
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activity-read-32457841
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agent:minimax-reader
[2] object · 4 fields
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activity-resolve-GSE31210
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accession_resolution
used array · 1 item
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data:geo:GSE31210
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agent:corpus-assay-engine
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dsl_catalogue_fingerprint
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lineage object · 4 fields
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sha256:40bf0b25ccc46f73e9b735cbf819457fa068b8ec405f1ef503c978221c53fa7e
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asset:data:geo:GSE31210 licence not read
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[3]
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[4]
execution.not_run
[5]
method.reader_named_unmapped
[6]
review.human_critique
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source_hashes object · 1 field
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32457841", "kind": "science-record", "revision": 7, "content_hash": "sha256:5bcb97b8f76f2a3a3c080109f847114ec3a89759c440b96ca3cbd7113b2d33e2", "created_at": "2026-11-01T15:41:02Z", "updated_at": "2026-11-01T22:01:40Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Immunoscore Predicts Survival in Early-Stage Lung Adenocarcinoma Patients.", "doi": "10.3389/fonc.2020.00691", "pmid": "32457841", "authors": ["Zihuan Zhao", "Dan Zhao", "Ji Xia", "Yi Wang", "Buhai Wang"], "journal": "Frontiers in oncology", "year": 2020, "abstract": "Background: The lung cancer staging system is insufficient for a comprehensive evaluation of patient prognosis. We constructed a novel immunoscore model to predict patients with high risk and poor survival. Method: Immunoscore was developed based on z-score transformed enrichment score of 11 immune-related gene sets of 109 immune risk genes. The immunoscore model was trained in lung adenocarcinoma cohort from The Cancer Genome Atlas (TCGA-LUAD) (n = 400), and validated in other two independent cohorts from Gene Expression Omnibus (GEO), GSE31210 (n = 219) and GSE68465 (n = 356). Meta-set (n = 975) was formed by combining all training and testing sets. Result: High immunoscore conferred worse prognosis in all sets. It was an independent prognostic factors in multivariate Cox analysis in training, testing and meta-set [hazard ratio (HR) = 2.96 (2.24-3.9), P < 0.001 in training set; HR = 1.99 (1.21-3.26), P = 0.006 in testing set 1; HR = 1.48 (1.69-2.39), P = 0.005 in testing set 2; HR = 2.01 (1.69-2.39), P < 0.001 in meta-set]. Immunoscore-clinical prognostic signature (ICPS) was developed by integrating immunoscore and clinical characteristic, and had higher C-index than immunoscore or stage alone in all sets [0.72 (ICPS) vs. 0.7 (immunoscore) or 0.59 (stage) in training set; 0.75 vs. 0.72 or 0.7 in testing set 1; 0.65 vs. 0.61 or 0.62 in testing set 2; 0.7 vs. 0.66 or 0.64 in meta-set]. Genome analysis revealed that immunoscore was positively correlated with tumor mutation burden (R = 0.22, P < 0.001). Besides, high immunoscore was correlated with high proportion of carcinoma-associated fibroblasts (R = 0.32, P < 0.001) in tumor microenvironment but fewer CD8+ cells infiltration (R = -0.28, P < 0.001). Conclusion: The immunoscore and ICPS are potential biomarkers for evaluating patient survival. Further investigations are required to validate and improve their prediction accuracy.", "claims": [{"id": "claim-method", "statement": "C-index of ICPS was compared with stage or immunoscore alone using “compareC” package (43).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32457841", "locator": "sections[8] \"Immunoscore-Clinical Prognostic Signature Construction\" paragraph 2", "quote": "C-index of ICPS was compared with stage or immunoscore alone using “compareC” package (43)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Data Availability Statement\nPublicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov, https://www.ncbi.nlm.nih.gov/geo.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32457841", "locator": "sections[23] \"Data Availability Statement\" paragraphs 1-2", "quote": "Data Availability Statement\nPublicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov, https://www.ncbi.nlm.nih.gov/geo."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "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:32457841"], "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. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE31210"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE31210"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:32457841", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fonc.2020.00691", "sha256": "sha256:6429bde39900be907390025cd959af48f9d562f8b4d0804ad157607236959383", "bytes": 54046, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fonc.2020.00691", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC7225293", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE31210", "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=GSE31210", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE31210", "version": null, "note": "Data Availability Statement\nPublicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov, https://www.ncbi.nlm.nih.gov/geo.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "Data Availability Statement\nPublicly available datasets were analyzed in this study. 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