Cheng Jian Biomedical

Cheng Jian Biomedical Provide NGS diagnostic services to the international and support
Association of Southeast Asian Nat

30/07/2018

How to therapy the cancer?
Surgical therapy: Surgical therapy is the earliest applied method of treating cancer, and it is also the first choice for many early cancer treatments. Many early cancers can be cured through successful surgery. Some cancer patients develop advanced disease and cannot undergo radical surgery. However, in order to alleviate the patient's pain and prolong the patient's life, surgery can also be performed. This type of surgery is called palliative surgery. For example, colon cancer obstructs the intestine and cannot defecate normally. A palliative operation of the large intestine is needed to relieve the obstruction of the tumor to the intestinal lumen. It is not possible to perform surgery on any cancer, such as blood cancer (ie leukemia).

Chemotherapy: Chemotherapy is the use of chemical drugs to treat cancer, generally refers to Western medicine anticancer drugs. These drugs can inhibit or kill cancer cells at different stages of cancer cell growth and reproduction for therapeutic purposes. However, existing chemical drugs also damage normal human cells while killing cancer cells. Therefore, different degrees of side effects such as nausea, vomiting, and hair loss often occur during chemotherapy. Currently, chemotherapy is mainly used for various types of leukemia and for patients who are inoperable but not sensitive to radiation therapy. In addition, it is also used as an adjuvant therapy after cancer surgery to kill cancer cells that are scattered or can only be found under the microscope, delaying or preventing cancer recurrence.

Ordinary radiation therapy: ordinary radiation therapy is to kill cancer cells with radiation to achieve therapeutic purposes. Some cancers have a good effect on radiotherapy, or are sensitive to radiotherapy, such as Hodgkin's disease, non-Hodgkin's lymphoma, leukemia, etc.; while others are not sensitive to radiotherapy, ie, poorly effective, such as pancreatic cancer, colon gland Tumor, chondrosarcoma and melanoma. Radiation therapy can effectively kill cancer cells and avoid tissue defects and deformities caused by surgery. When cancer has spread to other tissues or moved elsewhere, the surgery cannot be completely removed, and radiotherapy can be used to kill cancer cells. Like chemotherapy, ordinary radiotherapy also causes damage to normal cells of the human body, so it has a series of side effects.

Immune cell therapy: Immune cell therapy is the latest technology developed in recent years. The principle is to directly put a large number of undifferentiated dendritic cells into the blood vessels in the tumor or around the tumor, which can quickly and massively enhance the ability of dendritic cells to recognize specific cancer cells. The dendritic cells can help the helper T cells to rapidly induce a large number of cytotoxic T lymphocytes (CTLs) to attack specific cancer cells in a short time. Recently, doctors can use tumor mutation burden to predict sensitivity to checkpoint inhibitor therapy in various solid tumor types reported to date. Early evidence suggests TMB is independent of PD-L1 expression, but TMB is correlated with higher response rate to checkpoint inhibitor. A minority of TMB-high tumors are also MSI-high. Tumor mutation load is associated with production of neoantigens which may be recognized by the immune system.

Target therapy: Targeted treatments have seen significant effects in the treatment of certain types of cancer since the late 1990s and are as effective in treating cancer as chemotherapy, but with fewer side effects than chemotherapy. Molecular target therapy is an immunotherapy that blocks cancer cells' specific growth factors or receptors. This therapy is like a "guided missile" that can accurately hit targets and inhibit specificity. The growth, metastasis and invasion of tumor cells avoid unnecessary side effects caused by the complete destruction of traditional anticancer drugs. For example: Epidermal growth factor receptor (EGFR), which affects the growth of lung cancer cells, affects the formation of neovascularization (VEGFR) on which lung cancer depends. If the message transmission process of these lung cancer growth is blocked, the growth of lung cancer can be effectively inhibited, and the damage to normal human tissues can be minimized. There are many modes of blocking, such as: specific binding of small molecule compounds (EGFR-TKI) to receptors, or binding of antibodies to specific receptors on the membrane of lung cancer cells, blocking these key points to inhibit cancer cell growth.

Why different price of NGS of cancer detection?The first, we must identify that the service provider’s assay is NGS or n...
25/07/2018

Why different price of NGS of cancer detection?
The first, we must identify that the service provider’s assay is NGS or nor NGS platform. Such as serum tumor marker, single nucleotide polymorphism and hot-spot are not NGS-based assay. NGS-based assay is classified four different degree sequence including, capture sequence, whole exon sequence and whole genome sequence. The whole genome sequence is most expensive, hot-spot sequence is most cheaper than others. You may think that one gen when check 10, 100, 1000 or whole sites, led to different cost and also have different sensitivity and specific assay. For example, BRCA gene have been reported have more than hundred pathogenic mutation so it is necessary to detected by capture sequence, whole exon sequence and whole genome sequence, but not hot spot or SNP assay.

23/07/2018

When were we need to do the cancer screen or Phamgenomic test?

For normal subject
The occurrence and development of tumors are affected by both genetic and environmental aspects. Among them, genetic tumors caused by genetic abnormalities account for about 5%-10%. Susceptible genotypes carrying certain genes increase the risk of cancer in individuals to some extent. Using tumor genetic testing methods, through the comprehensive analysis of individualized genetic factors and environmental factors, we can understand the genetic variation of tumorigenesis and development in human body, and thus assess the relative risk of cancer incidence, which can be positively personalized at the earliest stage. Health management, thus effectively preventing the occurrence and development of diseases, reducing medical expenses, improving and maintaining the health status of the subjects, and enjoying a high quality of life. So, high-risk populations with a family history of genetics, breast proliferative lesions, and healthy populations. Early cancer screen or detect in both healthy and high-risk populations at a stage before symptom onset that may lead to decreased morbidity and increase survival rate. Moreover, in some clinic situations treatment may require only surgery if we could identified cancer cell by early detection.

For cancer patient
With the discovery of tumor-driven genes and the research and application of corresponding targeted drugs, cancer therapy has embarked on the path of gene-oriented individualized therapy. The targeted therapy has high efficiency and low toxic and side effects, which can improve the quality of life of lung cancer patients to a greater extent. However, targeted therapeutics only act on tumor cells with specific gene mutations, and for tumor cells that do not contain specific gene mutations, targeted drugs are even less effective than chemotherapy drugs. Therefore, the internationally authoritative "NCCN* Clinical Practice Guidelines for Non-Small Cell Lung Cancer" clearly states that patients must undergo appropriate genetic testing before receiving targeted therapy.

It will help patient some benefit as follow:
1. Guide targeted drugs and surgical options: According to the results of genetic testing, assist doctors to select the correct targeted drugs and reasonable surgical methods for patients, and develop precise treatment plans.
2. Assess the risk of recurrence: assist in assessing the risk of cancer recurrence, early prevention, and reasonable treatment.
3. Do a good job of close relatives prevention: determine the heritability of the tumor, assess the risk of the patient's close relatives, and do early prevention and intervention.
4. Reproductive health interventions: For patients who are expected to have a healthy next generation, consider reducing the chances of having a child with a malignant tumor through assisted reproduction.

19/07/2018

Why chose NGS to detect cancer?
Aforementioned cancer cell can be detected by different methods. However, different methods have its own advantage and disadvantage.

maging
The root of the problem is one of scale. A typical cell in the human body is 10 μm in diameter, with a volume of only 1 pL. Hence every 1 cm3 (1 g) of solid tissue contains approximately 109 or one billion cells; the entire human body is estimated to contain approximately 1014 cells. Because a malignant clone evolves from a single cell, initially one would need a detectability of 10−14, an inconceivably small number, to detect the genesis of a tumor. Unfortunately, the present detection threshold for solid tumors is approximately 109 cells (1 g = 1 cm3) growing as a single mass. The tumor was detected about 0.6 cm or more, and the examination for cancer with cavity organs was not good, such as lung cancer, breast cancer, digestive tract-large intestine, re**al cancer.

Tumor Markers
Unfortunately, most of the available tumor markers are unsuitable for early detection as they possess inadequate sensitivity for small cancers or premalignant lesions and lack specificity for malignancy. These twin problems of limited sensitivity and specificity, especially when combined with the low prevalence of most cancers in the community, limit the use of most of the available tumor markers in population-based screening for early malignancy. So, the lower sensitivity and specificity may often have detected when the tumor has developed to a considerable size or has been transferred to other organs.

Circulating tumor DNA (ctDNA)
Although biomarkers such as prostate-specific antigen (PSA), have been known and used for decades to attempt to guide prognostic and therapeutic decisions, the recent revolution in molecular biology, with the rise of high-throughput sequencing and increased molecular characterization of tumor tissue has led to an exponential increase in attempts to measure and target aberrant pathways at the molecular level. However, utility of ctDNA by NGS technical, tumor can be detected in about 0.2 cm in size, with an accuracy of more than 93%. It can screen 10 kinds of cancers at a time, and only need to take blood. The ctDNA is derived from cancer cells and contains the mutation information of tumor cells. Through gene sequencing, the mutation patterns and sites can be understood, and the patient's condition and recovery status, treatment effect and drug resistance evaluation can be grasped in time. Effectively monitor the status of cancer patients to achieve the purpose of the right medicine.

16/07/2018

How to detect cancer cell?

Circulating tumor DNA (ctDNA)
As early as 1948, researchers found free DNA in peripheral blood. Thirty years later, the researchers found that the DNA content in the peripheral blood of patients with tumors was significantly higher than that of normal people. The researchers then detected the mutated proto-oncogene in the peripheral blood of the patients, and consistent with the primary tumor, confirmed the circulating tumor DNA (circulating) The presence of tumor DNA, ctDNA).
Compared with normal people, tumor patients have a large amount of ctDNA, which is derived from apoptotic or/and necrotic tumor cells. These DNA fragments derived from tumor tissues or circulating tumor cells (CTC) carry tumor specificity. The s*x DNA sequence enters the blood circulation and forms circulating tumor DNA that can be detected in the peripheral blood.

One of the important bottlenecks encountered in clinical individualized diagnosis and treatment is that most patients with cancer cannot perform tissue biopsy. Taking lung cancer as an example, 70-80% of patients with newly diagnosed non-small cell lung cancer have reached the advanced stage and lost their chance of surgery. Organizational access difficulties; another important bottleneck comes from the ubiquitous tumor heterogeneity, there are differences between different cells in the same lesion, there are differences between primary and metastatic lesions, and there may be differences between different metastases. Both of them pose challenges to the detection of tumor tissue as a test sample and circulating tumor DNA fragments present in peripheral blood undoubtedly become the gospel of these patients. The specific sequence in the circulating tumor DNA maintains a high degree of consistency with the tumor-specific sequence derived from the tissue sample, and the type and quantity of the mutation are analyzed by sequencing the circulating tumor DNA.

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2nd Floor, No. 190, Section 1, Zhongshan Road, Yonghe District
Yonghe
234

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