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PROSTATE CANCER前列腺癌
115426peopleAnnual number of new patients in China
34628peopleThe number of patients benefited from genetic testing each year
MiCheck®
Product introductionMiCheck® is a product that uses Abbott Architect or Roche Cobas analyzers to test three blood biomarkers that have been validated and used in clinical testing to assess a patient's risk of developing aggressive prostate cancer.
Product advantages

High specificity

Only two companies in the world can clearly identify malignant prostate cancer like this.Non-cancer patients and patients with mild tumors do not need treatment now.

High accuracy

The accuracy of this product is higher than competing products OPKO, 4K Score.

Detection significance

Determining whether biopsy is needed

Intended for
For patients with Gleason score ≥4+3
Prostatype®
Product introductionProstatype® is the world's leading prognostic risk assessment gene detection system for prostate cancer, combining tumor cell gene expression information and clinical information (PSA, Gleason score, tumor stage) to comprehensively assess tumor aggressiveness and prostate cancer-specific mortality risk.
Product advantages

Authorized certification

It is an IVD product with CE certification

Accurate detection

Using three genes, IGFBP3, F3, and VGLL3, significantly improves the prediction of prostate cancer mortality

Detection significance

1. Determining whether surgery is needed

2. Determine whether adjuvant or neoadjuvant therapy is needed

Intended for
Newly diagnosed prostate cancer patients
Qianxianan™
Product introductionQianxianan™ detects 648 prostate cancer-related genes at one time. It can comprehensively evaluate prognosis, endocrine, chemotherapy, targeting, immune drug efficacy, neuroendocrine differentiation, hereditary prostate cancer and other hereditary tumor risks and other issues related to diagnosis and treatment . It can also detect TMB, MSI, and other driving genes of tumor development, suggesting the possibility of using immune and targeted drugs.
Product advantages

Comprehensive testing coverage

Covering the application scenarios of patients of various stages, covering all exons and part of introns of related genes, detecting single nucleotide variation (SNV), small insertion/deletion variation, copy number variation (CNV), gene Fusion

Reliable detection method

The product has undergone rigorous methodological performance verification.The blood and tissue consistency of mCRPC is more than 90%, and the data has been published in JNCCN (IF=11.908)

Professional report interpretation

With the largest prostate cancer gene database and abundant clinical data in China, the report interpretation is more in line with Chinese characteristics and suitable for clinical treatment 

Fruitful academic achievements

Panels based on ctDNA detection have published many high-scoring articles, respectively in J Urol. (IF=7.45) and JNCCN (IF=11.908), etc. Another real-world multicenter study of rare germline deleterious mutations in Chinese prostate cancer patients was published in CTM (IF=11.492)

Detection significance

Chosing a treatment

It can indicate prognosis, neuroendocrine differentiation, the efficacy of endocrine drugs、chemotherapy drugs、 PARPi 、other targeted drugs and immune drugs .

Providing genetic counseling

It can indicate the risk of prostate cancer and other hereditary tumors.

Intended for
All prostate cancer patients
mCRPC patients at any time
Highly suspected hereditary prostate cancer patients
Pushengta®
Product introductionPushengta® detects 86 prostate cancer-related genes.The product completely fits the path of diagnosis and treatment, covering the application scenarios of patients of various stages.It can comprehensively answer clinical questions such as NEPC, the efficacy of new endocrine therapy, PARPi/platinum chemotherapy sensitivity, prognostic risk, chemotherapy efficacy, immune efficacy, genetic risk, etc., helping guide medication in each line of treatment.
Product advantages

Reliable detection method

The product has undergone rigorous methodological performance verification.The blood and tissue consistency of mCRPC is more than 90%, and the data has been published in JNCCN (IF=11.908)

Professional report interpretation

With the largest prostate cancer gene database and abundant clinical data in China, the report interpretation is more in line with Chinese characteristics and suitable for clinical treatment 

Fruitful academic achievements

Panels based on ctDNA detection have published many high-scoring articles, respectively in J Urol. (IF=7.45) and JNCCN (IF=11.908), etc. Another real-world multicenter study of rare germline deleterious mutations in Chinese prostate cancer patients was published in CTM (IF=11.492)

Detection significance

Chosing a treatment

It can indicate prognosis, neuroendocrine differentiation, the efficacy of endocrine drugs、chemotherapy drugs、 PARPi 、other targeted drugs and immune drugs

Providing genetic counseling

It can indicate hereditary prostate cancer risk

Intended for
All prostate cancer patients
mCRPC patients at any time
Highly suspected hereditary prostate cancer patients
Pushengqiang-HRR™
Product introductionPushengqiang-HRR™ detects 14 HRR genes related to the FDA-approved olaparib companion diagnosis, which can specifically screen the beneficiaries of olaparib.
Product advantages

Accreditation by authority

In 2020,GloriousMed was awarded the high-quality unit for HRR testing and calibration items by the Urology Branch of the Chinese Medical Association

Reliable detection method

The product has undergone rigorous methodological performance verification.The blood and tissue consistency of mCRPC is more than 90%, and the data has been published in JNCCN (IF=11.908)

Professional report interpretation

With the largest prostate cancer gene database and abundant clinical data in China, the report interpretation is more in line with Chinese characteristics and suitable for clinical treatment 

Fruitful academic achievements

Panels based on ctDNA detection have published many high-scoring articles, respectively in J Urol. (IF=7.45) and JNCCN (IF=11.908), etc. Another real-world multicenter study of rare germline deleterious mutations in Chinese prostate cancer patients was published in CTM (IF=11.492)

Detection significance

Evaluation of the efficacy of PARPi

Determining whether PARPi can be used

Evaluation of the efficacy of platinum

Determining whether platinum can be used

Intended for
Metastatic prostate cancer patients
Qianxianhui™
Product introductionQianxianhui™ detects 12 high-frequency genes in prostate cancer, which can indicate prognosis, the efficacy of adjuvant and neoadjuvant therapy, and prolong the time for patients to progress to mCRPC.
Product advantages

Selecting core genes

It detects AR, BRCA1/2, TP53, PTEN and other prostate cancer high-frequency genes, which can be used as a general test product for early HSPC patients 

Accurate test results

GloriousMed has passed the CAP authoritative certification and complies with the IS015189 international quality system standard. The sensitivity and specificity of the detection were greater than 99%

Professional report interpretation

With the largest prostate cancer gene database and abundant clinical data in China, the report interpretation is more in line with Chinese characteristics and suitable for clinical treatment

Fruitful academic achievements

Panels based on ctDNA detection have published many high-scoring articles, respectively in J Urol. (IF=7.45) and JNCCN (IF=11.908), etc. Another real-world multicenter study of rare germline deleterious mutations in Chinese prostate cancer patients was published in CTM (IF=11.492)

Detection significance

Prognostic analysis

It can indicate prognosis for risk stratification to determine whether surgery, adjuvant or neoadjuvant therapy is needed.

Medication guidance

It can indicate the efficacy of endocrine drugs、PARPi、AKTi、platinum and neuroendocrine differentiation to guide medication.

Intended for
Early-stage prostate cancer patients
Qianxianchangan
Product introductionQianxianchangan is a 3-time gene detection product for mHSPC patients with initial treatment, poor treatment effect, recurrence and progression;for CRPC patients before medication, after a period of treatment resistance、progression . It can dynamically monitor the changes of genes, so as to realize the precise whole-process management of prostate cancer and assist clinical decision-making.
Product advantages

Comprehensive testing coverage

Covering the application scenarios of patients of various stages, covering all exons and part of introns of related genes, detecting single nucleotide variation (SNV), small insertion/deletion variation (Indel), copy number variation (CNV), gene Fusion

Reliable detection method

The product has undergone rigorous methodological performance verification.The blood and tissue consistency of mCRPC is more than 90%, and the data has been published in JNCCN (IF=11.908)

Professional report interpretation

With the largest prostate cancer gene database and abundant clinical data in China, the report interpretation is more in line with Chinese characteristics and suitable for clinical treatment 

Fruitful academic achievements

Panels based on ctDNA detection have published many high-scoring articles, respectively in J Urol. (IF=7.45) and JNCCN (IF=11.908), etc. Another real-world multicenter study of rare germline deleterious mutations in Chinese prostate cancer patients was published in CTM (IF=11.492)

Detection significance

Prognostic analysis

It can indicate prognosis for risk stratification to choose ADT combination regimens

Dynamic monitoring

It can dynamically monitor gene changes to indicate the efficacy of endocrine drugs、chemotherapy drugs、targeted drugs、immune drugs and neuroendocrine differentiation at various nodes such as initial treatment, drug resistance, and relapse.

Intended for
mHSPC patients with initial treatment, poor treatment response or recurrent progression
CRPC patients with drug resistance/progression before and after treatment for a period of time
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