Gwajin kwayoyin cutar kansar Amurka yayi nasarar magance sarcoma mai taushi

Share Wannan Wallafa

A ranar 10 ga Yuli, 2015, Cibiyar Ciwon Kankara ta Kasa (NCI) ta sanar da cewa mafi girman madaidaicin gwajin asibiti a tarihi ya fara daukar marasa lafiya. Wannan gwajin zai dauki majinyata 1,000 masu fama da cutar kansa kuma za su yi nazarin magunguna sama da 20 da aka yi niyya a lokaci guda. (Hadi da magungunan da aka yi kasuwa kuma har yanzu suna cikin bincike na asibiti) Amfanin mutanen da ke da maye gurbin kwayar cutar kansa ko wuce gona da iri. Wannan zai ƙara ƙarfafawa da haɓaka matsayin Amurka a cikin binciken kwayoyin cutar kansa, ganowa da kuma maganin cutar kansa. 

Kasar Amurka ita ce kasar da ta fi samun ci gaba a gwajin kwayoyin cutar kansa da kuma maganin da aka yi niyya, inda aka samar da kamfanoni da fasahohin da suka fi samun ci gaba, da manyan cibiyoyin kula da cutar kansa da kwararru, da kuma samar da magungunan yaki da cutar kansa. Marasa lafiya na ciwon daji za su taimaka game da 82% na marasa lafiya samun niyya magungunan magani ko magungunan gwaji na asibiti ta hanyar gwajin cikakken kwayar cutar kansa (ba wani ɓangare na gwajin kwayoyin halittar cikin gida ba) da babban bincike na bayanai.

Tarihin likita na yanzu:

The patient was 55 years old and female. The clinical manifestation was a mass on the left chest wall, the largest at more than 6 cm. Tumor tissue biopsy sampling, pathological examination results: spindle cell proliferation, initial diagnosis of malignant spindle cell tumor grade 2 (Figure 1, A and B). Immunohistochemistry results were positive for S-100 and CD34 (Figure 1, C and D). In the high power field of vision, each field of vision can see 6/10 mitotic phase, but no necrosis. According to the FNCLCC guidelines for the histopathological grade of soft tissue sarcoma, this case is difficult to diagnose tumor should be intermediate.

Mai haƙuri ya fara amfani da 75 mg / m2 Adriamycin (Adriamycin®) dabevacizumab. The patient reduced the dose of sorafenib to 200 mg per day due to grade 2-3 hand and foot syndrome caused by sorafenib. In addition, the patient was well tolerated by the treatment and the treatment lasted for 7 months.

Clinical trial: The patient participated in a phase I clinical trial of bevacizumab, temsirolimus and sorafenib in the treatment of advanced cancer (clinical trial number: NCT01187199). Sorafenib is a small molecule kinase inhibitor that has certain effects on BRAF, VEGFR 1/2/3, PDGFRB, RAF and other signaling pathways and can inhibit the activity of KIAA1549-BRAF. Both KIAA1549-BRAF and PTEN deletion can overactivate the mTOR pathway. Therefore, sorafenib combined with temsirolimus together inhibits the BRAF and mTOR pathways, which may overcome tissue resistance to BRAF single targeted therapy.

The protocol of this clinical trial was: oral administration of 200 mg sorafenib twice a day, intravenous injection of 20 mg temsirolimus on days 1, 8 and 15 and intravenous injection of 10 mg / kg bevacizumab every 21 days.

Tabbatacce:

After two cycles of treatment, the maximum linear measurement of the patient’s tumor was reduced by 25% (Figure 2, A and B), the condition was stable and the index was only below the standard for partial response. Secondary chest pain was reduced, and breathing difficulties were relieved. In the course of treatment, symptomatic treatment is required for hypertension (grade 3) caused by bevacizumab. The patient reduced the dose of sorafenib to 200 mg per day due to grade 2-3 hand and foot syndrome caused by sorafenib. In addition, the patient was well tolerated by the treatment and the treatment lasted for 7 months.

Cancer full genetic testing:

Studies have shown that the genetic changes that occur when you develop cancer are different, and you respond differently to drugs. Targeted drugs can specifically act on genes that cause tumor growth, and thus have better efficacy. Among the hundreds of oncogenic genes that have been discovered, each gene may have many different changes, so the genetic changes of each cancer patient are unique. Genetic testing can help patients and doctors guide treatment and discover new treatments.

Of the cancer genetic testing patients, 82% of the test results were later used in actual treatment, including: 1. Finding an approved treatment for the patient’s tumor genetic changes; 2. Finding an approved treatment for cancer New drugs for other types of cancer with the same gene changes, such drugs are likely to have significant effects on the patient’s tumor; 3. Find a clinical trial, although the test drug used does not directly affect the genes of the patient’s tumor, but the effect Because of the related signal pathway, it may also have a good effect.

Patients can obtain the most advanced cancer gene detection in the United States or China through the global cancer doctor network cooperative research institution, find gene mutations and targeted drugs, and obtain the treatment opinions of American cancer experts. Global Oncologist Network is the most professional anti-cancer institution in China, which can provide patients with the world’s most anti-cancer technology. Because the patient’s pathological tissue is very precio
us, the detection level of the testing organization and the big data analysis ability are very different. It is recommended that patients choose the most certified organization for global oncologist network for testing.

For details on sarcoma treatment and second opinion, do call us at +91 96 1588 1588 or write to cancerfax@gmail.com.

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