I-CAR T-Cell therapy yesimila ebuchosheni bengane

Yabelana ngalokhu okuthunyelwe

Disemba 2021: CAR T-Cell therapy is currently approved for some forms of leukemia, lymphoma, and multiple myeloma. Researchers have now also developed the corresponding GD2 CAR T-cell therapy for the treatment of neuroblastoma, i.e., childhood brain tumors. Lung cancer, stomach cancer, liver cancer, breast cancer, and other adult cancers have the highest incidence. When discussing children’s cancer, many people instinctively believe that it is identical to adult cancer.

I-CAR T Cell therapy ye-neuroblastoma yezingane

However, whether it is the cause of cancer or the type of cancer, there is a significant difference between childhood cancer and adult cancer. The most frequent childhood tumour is i-neuroblastoma, which is more common than lung cancer, gastric cancer, and other cancers. Neuroblastoma can account for half of all cancers in children under the age of five, greatly exceeding the proportion of various malignancies in adult cancers.

Kodwa-ke, izinga lokusinda leminyaka emi-5 leziguli ze-neuroblastoma alikabi lihle kakhulu, futhi cishe amaphesenti angama-40 kuya kwangu-50 eziguli azikakwazi ukuthola ukwelashwa kwesikhathi eside. Ngokufanayo, uma isimila sibuya, ingane isesengcupheni, njengoba kwenzeka lapho umdlavuza omdala ubuya.

Ukwelashwa kwamaseli e-CAR T kwethumba ebuchosheni lobungane 1.1

Is there a new treatment available?

Ukwelashwa kwamaseli e-CAR-T has opened up a whole new universe in the field of advanced relapse and refractory B-cell cancers in recent years, and it has also allowed people to witness how effective it can be.

As a result, researchers have created a GD2-CAR-T cell therapy for the treatment of neuroblastoma for the matching target of neuroblastoma. The findings of the clinical study were published in the most recent issue of “Science Translational Medicine.”

Lolu cwaningo lufake isamba sezingane eziyi-12 ezine-neuroblastoma ebuyele emuva/eyirefractory. Sekukonke, umuthi ubekezelelwe kahle, futhi akukho miphumela engemihle ebihlosiwe eyabonwa. Naphezu kweqiniso lokuthi ayizange ifinyelele impendulo yomtholampilo eyinhloso, abacwaningi baqaphele inzuzo yokwelapha yangempela kwabanye abantu.

Isiguli esingu-25/010 intombazane eneminyaka engu-8 ubudala ene-neuroblastoma metastase enkulu, okuhlanganisa ama-metastase abalulekile amathambo (ukuphindaphinda ngemva kokwelashwa komugqa wesine). Isimo esijwayelekile sibe ngcono kakhulu ngemuva kwezinsuku ezingama-28 Ukwelashwa kwamaseli e-CAR-T, futhi izicubu zesimila nazo zibonise i-necrosis yesimila esandile.

Patient 25/013 is a 10-year-old girl who has had five treatments for multiple recurrent localised neuroblastomas. There were tumour nodules in the neck before therapy, but no distant metastases. An MRI showed that the tumour had shrunk after treatment. Following a tumour biopsy, it was discovered that the tumour had significant necrosis.

Isiguli esingu-25/018 siyingane eneminyaka engu-10 ubudala ene-neuroblastoma ephindaphindayo esabalale emzimbeni wayo wonke. Waba nezikhathi ezintathu ngaphambi nangemva kwalokho, futhi izinkinga zakhe zadamba ngenxa yokwelashwa.

However, while this study has demonstrated that the treatment is effective, after experiencing the peak of CAR-T cell therapy, the long-term expansion of CAR-T cells is not visible, making the treatment effect ineffective. It finally resulted in tumour recurrence, however, before that, this therapy helped 013 and 018 live for approximately 5 months longer.

Although this new CAR-T cell therapy cannot match the efficacy and durability of CD19-CAR-T cell therapy in haematological cancers, it demonstrates that CAR-T cell therapy can still be employed in the entity once a suitable target is identified. In the treatment of tumours, it has potent anti-tumor effects. To improve its therapeutic efficacy in solid malignancies, researchers will combine CAR-T activation with immune checkpoint drugs (PD-1 inhibitors).

The safety of this solid tumour CAR-T cell treatment is currently assured. The patient got CRS as a result of the medication, although no major neurotoxic reactions occurred. Medical teams receiving CAR-T cell therapy may soon have to respond to CRS as a matter of course. CAR-T cell therapy still has a long way to go in terms of overcoming solid tumours, but it will get there someday.

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Okuningi Okuzohlolwa

Ukuqonda I-Cytokine Release Syndrome: Izimbangela, Izimpawu, Nokwelashwa
Ukwelashwa kwe-CAR T-Cell

Ukuqonda I-Cytokine Release Syndrome: Izimbangela, Izimpawu, Nokwelashwa

I-Cytokine Release Syndrome (CRS) iwukusabela kwamasosha omzimba okuvame ukubangelwa izindlela zokwelapha ezithile ezifana ne-immunotherapy noma i-CAR-T cell therapy. Kuhilela ukukhululwa ngokweqile kwama-cytokines, okubangela izimpawu ezisukela kumkhuhlane nokukhathala kuya ezinkingeni ezingase zibeke ukuphila engozini njengokulimala kwesitho. Ukuphatha kudinga ukuqapha ngokucophelela kanye namasu okungenelela.

Iqhaza labezimo eziphuthumayo empumelelweni yokwelashwa kwe-CAR T Cell
Ukwelashwa kwe-CAR T-Cell

Iqhaza labezimo eziphuthumayo empumelelweni yokwelashwa kwe-CAR T Cell

Abezimo eziphuthumayo badlala indima ebalulekile empumelelweni yokwelashwa kwe-CAR T-cell ngokuqinisekisa ukunakekelwa kwesiguli okungenamthungo kuyo yonke inqubo yokwelashwa. Banikeza ukwesekwa okubalulekile ngesikhathi sokuthutha, ukuqapha izimpawu ezibalulekile zeziguli, nokuphatha ukungenelela kwezokwelapha eziphuthumayo uma izinkinga ziphakama. Ukusabela kwabo okusheshayo kanye nokunakekelwa kochwepheshe kunomthelela ekuphepheni okuphelele nasekusebenzeni ngempumelelo kokwelashwa, kusiza uguquko olushelelayo phakathi kwezilungiselelo zokunakekelwa kwezempilo kanye nokwenza ngcono imiphumela yesiguli endaweni eyinselele yezindlela zokwelapha ezithuthukisiwe zamaselula.

Dinga usizo? Ithimba lethu likulungele ukukusiza.

Sifisela ukululama okusheshayo kothandekayo wakho futhi oseduze.

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