luminal B breast carcinoma
disease diseaseOn this page
Also known as Luminal BLuminal B breast cancerLuminal B estrogen receptor positive subtype of breast carcinomaLuminal B oestrogen receptor positive subtype of breast carcinomaLuminal B subtype of breast carcinoma
Summary
luminal B breast carcinoma (MONDO:0021115) is a cancer with 7 GWAS associations across 7 studies and 9 clinical trials. Top therapeutic interventions include cyclophosphamide anhydrous and oleclumab. A subtype of breast tumor luminal A or B — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
- GWAS associations: 7
- Clinical trials: 9
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | luminal B breast carcinoma |
| Mondo ID | MONDO:0021115 |
| DOID | DOID:0080674 |
| NCIT | C53555 |
| UMLS | C3642346 |
| MedGen | 770986 |
| Is cancer (heuristic) | yes |
Also known as: Luminal B · Luminal B breast cancer · Luminal B breast carcinoma · Luminal B estrogen receptor positive subtype of breast carcinoma · Luminal B oestrogen receptor positive subtype of breast carcinoma · Luminal B subtype of breast carcinoma
Data availability: 7 GWAS associations (7 studies).
Disease family
Classification path: human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › carcinoma › breast carcinoma › breast carcinoma by gene expression profile › breast tumor luminal A or B › luminal B breast carcinoma
Related subtypes (1): luminal A breast carcinoma
Genetics & variants
GWAS landscape
7 GWAS associations across 7 studies. Top hits map to 4 distinct genes (as reported by GWAS).
Top associations by p-value
| rsID | p-value | Gene | Risk allele | Odds ratio |
|---|---|---|---|---|
| rs13258434 | 2e-09 | NACA4P - LINC02845 | G | 0.03 |
| rs1243184 | 2e-08 | MLLT10 | T | 0.03 |
| rs10873406 | 1e-07 | GPR68 - CCDC88C | G | 0.02 |
| rs10890844 | 2e-07 | C11orf65 | C | 0.02 |
| rs7589172 | 3e-07 | RPS2P18 - CDCA7 | A | 0.02 |
| rs4752568 | 3e-07 | FGFR2 | C | 0.02 |
| rs12403443 | 4e-07 | KIF1B | A | 0.02 |
Top studies (by case count)
| Study | Lead author | Year | Cases | Controls | Title |
|---|---|---|---|---|---|
| GCST90446471 | Sun X | 2024 | 16,499 | 0 | Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants that Confer Risk for Breast Cancer. |
| GCST90446472 | Sun X | 2024 | 16,499 | 0 | Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants that Confer Risk for Breast Cancer. |
| GCST90454346 | Zhang H | 2020 | 13,800 | 91,477 | Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses. |
| GCST90454347 | Zhang H | 2020 | 13,800 | 91,477 | Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses. |
| GCST90446468 | Sun X | 2024 | 12,414 | 0 | Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants that Confer Risk for Breast Cancer. |
| GCST90446473 | Sun X | 2024 | 5,859 | 0 | Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants that Confer Risk for Breast Cancer. |
| GCST90319679 | Hsu YC | 2023 | 234 | 0 | The largest genome-wide association study for breast cancer in Taiwanese Han population. |
Variant details and genetic-evidence tiers
Tier distribution (top 50 variants)
| Tier | Variants |
|---|---|
| Tier 1: coding | 0 |
| Tier 2: splice/UTR | 0 |
| Tier 3: regulatory | 0 |
| Tier 4: intronic/intergenic | 7 |
MAF distribution
| Bucket | Variants |
|---|---|
| common (>=0.05) | 7 |
| low_freq (0.01-0.05) | 0 |
| rare (<0.01) | 0 |
| unknown | 0 |
Functional consequences
| Consequence | Count |
|---|---|
| intron_variant | 5 |
| intergenic_variant | 2 |
Top variants
| rsID | Chr | Pos | Alleles | MAF | Consequence | Gene | p-value | Tier |
|---|---|---|---|---|---|---|---|---|
| rs13258434 | 8 | 101379857 | G>A,T | 0.05 | intergenic_variant | NACA4P - LINC02845 | 2e-09 | Tier 4: intronic/intergenic |
| rs1243184 | 10 | 21643008 | T>C | 0.05 | intron_variant | MLLT10 | 2e-08 | Tier 4: intronic/intergenic |
| rs10873406 | 14 | 91255717 | G>A,T | 0.05 | intergenic_variant | GPR68 - CCDC88C | 1e-07 | Tier 4: intronic/intergenic |
| rs10890844 | 11 | 108463400 | T>C | 0.05 | intron_variant | C11orf65 | 2e-07 | Tier 4: intronic/intergenic |
| rs7589172 | 2 | 173342742 | A>C | 0.05 | intron_variant | RPS2P18 - CDCA7 | 3e-07 | Tier 4: intronic/intergenic |
| rs4752568 | 10 | 121571027 | C>G,T | 0.05 | intron_variant | FGFR2 | 3e-07 | Tier 4: intronic/intergenic |
| rs12403443 | 1 | 10363930 | A>G | 0.05 | intron_variant | KIF1B | 4e-07 | Tier 4: intronic/intergenic |
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 9.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 4 |
| PHASE2 | 3 |
| PHASE3 | 1 |
| PHASE1/PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06585969 | PHASE3 | WITHDRAWN | A Randomised Trial Comparing Trastuzumab Deruxtecan to CDK4/6 Inhibitors in Non-luminal A, ER-positive/HER2-low Metastatic Breast Cancer |
| NCT03875573 | PHASE2 | ACTIVE_NOT_RECRUITING | Neo-adjuvant Chemotherapy Combined With Stereotactic Body Radiotherapy to the Primary Tumour +/- Durvalumab, +/- Oleclumab in Luminal B Breast Cancer: |
| NCT03356860 | PHASE1/PHASE2 | COMPLETED | Safety and Efficacy of Durvalumab Combined to Neoadjuvant Chemotherapy in Localized Luminal B HER2(-) and Triple Negative Breast Cancer. |
| NCT05163106 | PHASE2 | COMPLETED | Neoadjuvant Treatment of Locally-advanced Breast Cancer Patients With Ribociclib and Letrozole |
| NCT05640778 | PHASE2 | UNKNOWN | Neoadjuvant Dalpiciclib Plus Aromatase Inhibitors in Luminal B/HER2-negative Breast Cancer (DANCER) |
| NCT06805084 | Not specified | ACTIVE_NOT_RECRUITING | Transcripts with Retained H/ACA Box SnoRNA Sequences As Biomarkers for Estrogen Dependence in Lum-B Breast Carcinomas |
| NCT03715959 | Not specified | COMPLETED | Nipple Aspirate Fluid in Detecting Breast Cancer |
| NCT03860740 | Not specified | COMPLETED | Effect of Physical Exercise on Tumor Proliferation of Luminal B Breast Cancer Patients |
| NCT04118062 | Not specified | COMPLETED | Communicating With Patients on Cancer Resistance to Treatment: the Development of a Communication Tool. (HECTOR) |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| CYCLOPHOSPHAMIDE ANHYDROUS | 4 | 1 |
| OLECLUMAB | 3 | 1 |
Related Atlas pages
- Drugs: Cyclophosphamide, Oleclumab