Patient-derived Organoid (PDO)

Invitrocue’s PDOs are 3D tumor models derived from biopsies or surgical specimens from human. These PDOs exhibit remarkable similarities to the genetics, phenotyping and heterogeneity of the original tumors. These unique features make them an invaluable tool for studying human tumor biology, disease progression and treatment responses.

Conventional in vitro cell lines may not fully represent the complexity of original  tumors and lead to poor translatability in clinical settings. This may potentially hinder the development of targeted therapies and personalized medicine in pharmaceutical industry. To overcome this limitation, Invitrocue re-creates the 3D tumor microenvironment by using our proprietary 3D cell culture technology developed in Onco-PDOTM.  By accessing our established tumor organoid biobank, we offer to you a series of drug-validated PDOs to support decision-making throughout your preclinical cancer drug and personalized therapeutic strategies.

Fig 1: Organoids for Preclinical Drug Discovery

Tumor collection

1

Breast Cancer
HER2 DAPI

Lung Cancer
CK5 EGFR2 DAPI

Colon Cancer  
E-cad  P-AKT DAPI

Ovarian Cancer
VIM HER2 PGRMC1 DAPI

Patient derived Organoids (PDO)

2

PDO derived Xenografts (PDO-X)

3

Applications

We are committed to offering reliable 3D tumor organoid models to advance your preclinical cell and drug development. Our cell models are highly customizable and can be tailored to meet your diverse needs.

In Vitro Drug Screening

Biomarker Identification

In vivo Testing

Tumor Biology

Drug Resistance Study

Personalized Medicine

Key Features and Advantages of Invitrocue’s PDO Services

IVQ’s Proprietary 3D Culture System

To improve the organoid formation rate and effectively retain tumor characteristics.

1

Diverse Tumor Collection

7 major solid tumors: Breast, Colorectal, Lung, Ovarian, Pancreatic, Gastric, and Nasopharyngeal cancer, and expanding.

2

High Clinical Translatability

Drug responses are clinically proven through IVQ’s Onco-PDOTM test, which has a 75-80% positive predictive accuracy and over 90% negative prediction rate.

3

Efficient In Vitro To In Vivo Transition

Validated with over 75% transplantation success rate from in vitro to in vivo.

4

Support High-Throughput Screening

PDOs can be expanded in vitro for large-scale drug screening.

5

Drug Resistance Profile Available

Drug resistance and patient treatment history profiles are accessible upon request.

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Type of Services

PDO Collections

In collaboration with hospitals globally, Invitrocue provides an extensive range of cutting-edge 3D patient-derived organoids (PDO) for academic and industry research. Our proprietary organoids culture technology accurately replicates the genetic, phenotypic and heterogeneous profiles of the original patient tumour. In addition, these organoids have been profiled with Standard of Care (SOC) drugs and validated for in vivo xenograft development. By leveraging this information, Invitrocue offers a ready-to-use, highly translatable  and cost-effective in vitro model to accelerate your preclinical drug screening and advance your strategies for personalized cancer treatment.

S/N Types of Cancer Biomarkers Drug Resistance
1. Breast Carcinoma
  • ER/PR/HER2 negative
  • HER2 gene amplification
  • PIK3CA mutations
  • KRAS mutations (G12C)
  • CK20
  • CDX2
  • BRAF
  • NRAS
  • EGFR (Exon 19, 20, 21 mutations)
  • PD-L1 (>90%)
  • TTF-1
  • Claudin-4
  • CK7
  • MAP4:RAF1 fusion
  • BCL2
  • β-catenin
  • Trastuzumab
  • Tamoxifen
  • Platinum-Based
  • Taxanes
  • 5-FU
  • Irinotecan
2. Colorectal Adenocarcinoma
3. Lung Carcinoma
4. Pancreatic Adenocarcinoma
5. Ovarian Adenocarcinoma
6. Nasopharyngeal Carcinoma
7. Esophageal Carcinoma
8. Bone Sarcoma

Table 1. Invitrocue’s PDOs, related tumor biomarkers and drug-resistant profile for preclinical in vitro and in vivo services.

Case Studies

Invitrocue is committed to develop innovative products and services. Our high-throughput PDO services enable rapid and accurate preclinical drug efficacy assessments for cancer therapeutics. This section demonstrates case studies that highlight the practical applications and successes of our PDO technology in in drug candidate selection and effective dose-response determination.

Case Study 1 (Lung Cancer PDO)

Tumour Info Details
Type Adenocarcinoma
Stage IV, Metastatic
Sampling site Left paravertebral muscle
Biomarkers EGFR positive (L858R exon 21 mutation)
INTEGRATED RESPONSE SCORE (IRS) SUMMARY
DRUGS IRS SCORE
Cisplatin
Carboplatin
C1-1 0.2uM
C1-2 1uM
C1-3 5uM
C1-4 10uM
C1-5 20uM

Figure 2. Rx Score of SOC Drugs and Test Articles on Lung Cancer PDO.

Lung PDO (PDOSG-001-P301) was treated with SOC drugs or test articles at various concentrations in specific 3D lung culture media. Rx score was determined at 72 hours. Increasing doses of test article showed a progressive dose response against Lung PDO and the effect is comparable to SOC drugs like Cisplatin and Carboplatin.

Case Study 2 (Pancreatic Cancer PDO)

Tumour Info Details
Type Pancreatic Cancer
Stage IV, Metastatic
Sampling site Liver
   
INTEGRATED RESPONSE SCORE (IRS) SUMMARY
DRUGS IRS SCORE
Paclitaxel

Regorafenib

No Drug Response
Cobimetinib + Everolimus
Cobimetinib + Panitumumab
Doxorubicin
Pemetrexed
Paclitaxel + Vinorelbine

Figure 3. Rx Score of SOC Drugs on Pancreatic Cancer PDO.

Pancreatic PDO was treated with SOC drugs in specific 3D pancreatic culture media. Rx score was determined at 72 hours. Drug resistance was observed with kinase inhibitor – Regorafenib.

Test article (NDE-001 and NDE-002) responses are represented by Rx.
Rx score indicates the percentage of cell death caused by test article treatments at 72 hours.