Ikki immunoterapiya preparatining kombinatsiyasi jigar saratonini davolash usulini o'zgartirishi mumkin

Ushbu xabarni baham ko'ring

For patients with unresectable jigar hujayralari karsinomasi (HCC), the first-line treatment options are limited, including local ablation, arterial-directed therapy, or external radiation therapy or chemotherapy. Sorafenib (Dogime) is currently the only approved system for patients with unresectable HCC. Sexual treatment plan. In 2017, the FDA approved regorafenib (Stivarga) and nivolumab (Opdivo) as second-line treatment options for patients who previously received sorafenib. The researchers believe that the combination of PD-L1 inhibitor durvalumab (Imfinzi) and CTLA-4 inhibitor tremelimumab may be the most appropriate clinical treatment combination.

A randomized, multicenter, phase III HIMALAYA trial (NCT03298451) divided previously untreated, unresectable HCC patients into four groups: 2 different durvalumab combined with tremelimumab combined treatment regimens, durvalumab monotherapy and sorafenib Monotherapy (picture). The researchers used overall survival (OS) as the primary endpoint and time to progression, progression-free survival (PFS), and objective response rate (ORR) as the secondary endpoints.

Durvalumab is a human IgG monoclonal antibody, a PD-L1 inhibitor that binds to PD-1 and CD80, allowing T cells to recognize and kill shish cells without the need for antibody-dependent and cell-mediated cytotoxic activity. Tremelimumab has a similar mechanism, inhibiting CTLA-4, a cell surface receptor mainly expressed in activated T cells. The hypothesis is that inhibition of CTLA-4 will increase the activity of PD-L1 inhibitors.

In the previous phase I / II study, 40 patients with HCC evaluated the safety and tolerability of the combination. The confirmed ORR was 17.5%, of which 7 patients had partial responses (7/40 patients), and the median response time was 8 weeks. The combination is well tolerated and there is no danger signal in patients with unrespectable HCC. Subsequent research is also underway. This is achieved through the synergistic effect of the two immunoterapiya drugs to achieve the ultimate anti-tumor effect. It is expected that there will be better clinical results.

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Ko'proq o'rganish uchun

Lutetium Lu 177 dotatat USFDA tomonidan GEP-NETS bilan kasallangan 12 va undan katta yoshdagi bolalar uchun tasdiqlangan.
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Lutetium Lu 177 dotatat USFDA tomonidan GEP-NETS bilan kasallangan 12 va undan katta yoshdagi bolalar uchun tasdiqlangan.

Lutetium Lu 177 dotatat, innovatsion davolash vositasi, yaqinda AQSh oziq-ovqat va farmatsevtika idorasi (FDA) pediatrik bemorlar uchun ruxsat oldi, bu bolalar onkologiyasida muhim bosqichni belgilab berdi. Ushbu tasdiq saratonning kamdan-kam uchraydigan, ammo an'anaviy davolash usullariga chidamliligini isbotlovchi neyroendokrin o'smalari (NETs) bilan kurashayotgan bolalar uchun umid nuridir.

Nogapendekin alfa inbakicept-pmln BCG-ga javob bermaydigan mushak invaziv bo'lmagan siydik pufagi saratoni uchun USFDA tomonidan tasdiqlangan.
Quviq saratoni

Nogapendekin alfa inbakicept-pmln BCG-ga javob bermaydigan mushak invaziv bo'lmagan siydik pufagi saratoni uchun USFDA tomonidan tasdiqlangan.

"Nogapendekin Alfa Inbakicept-PMLN, yangi immunoterapiya, BCG terapiyasi bilan birgalikda siydik pufagi saratonini davolashda va'da beradi. Ushbu innovatsion yondashuv immunitet tizimining javobidan foydalangan holda saratonning o'ziga xos belgilarini maqsad qilib qo'yadi va BCG kabi an'anaviy davolash usullarining samaradorligini oshiradi. Klinik sinovlar bemorning yaxshilangan natijalarini va siydik pufagi saratonini davolashda potentsial yutuqlarni ko'rsatuvchi dalda beruvchi natijalarni ko'rsatadi. Nogapendekin Alfa Inbakicept-PMLN va BCG o'rtasidagi sinergiya qovuq saratonini davolashda yangi davrni e'lon qiladi.

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