I-Fruquintinib igunyazwe yi-USFDA kumdlavuza we-metastatic colorectal refractory

I-Fruquintinib igunyazwe yi-USFDA kumdlavuza we-metastatic colorectal refractory

Yabelana ngalokhu okuthunyelwe

I-Food and Drug Administration igunyaze i-fruquintinib (i-Fruzaqla, i-Takeda Pharmaceuticals, Inc.) ngoNovemba 8, 2023, ezigulini ezikhulile ezinomdlavuza we-metastatic colorectal (mCRC) ezithole ukwelashwa okukhethekile kwangaphambili.

Ukusebenza kwahlolwa ku-FRESCO-2 (NCT04322539) kanye ne-FRESCO (NCT02314819). Isivivinyo se-FRESCO-2 (NCT04322539) sihlole iziguli ezingama-691 ezine-mCRC ezithole ukuqhubeka kwesifo ngemuva kwe-fluoropyrimidine-, oxaliplatin-, i-irinotecan-based chemotherapy, i-anti-VEGF biological therapy, i-anti-EGFR biological therapy (uma uhlobo lwasendle lwe-RAS) lwangaphambilini. okungenani eyodwa ye-trifluridine/tipiracil noma i-regorafenib. Kwakuwucwaningo lwamazwe ngamazwe, olugxile ezindaweni eziningi, olungahleliwe, olungaboni kabili, olulawulwa yi-placebo. Isivivinyo se-FRESCO, isifundo se-multicenter e-China, sihlole iziguli ezingama-416 ezine-metastatic umdlavuza colorectal owathola ukuqhubekela phambili kwesifo kulandela i-fluoropyrimidine-, i-oxaliplatin, kanye ne-chemotherapy esekelwe ku-irinotecan.

Kuzo zombili izinhlolo, iziguli zabelwa ngokungahleliwe ukuthi zithole i-fruquintinib 5 mg ngomlomo kanye ngosuku noma i-placebo ezinsukwini zokuqala ezingama-21 zomjikelezo ngamunye wezinsuku ezingama-28. Baphinde bathola ukunakekelwa okungcono kakhulu okusekelayo. Iziguli zalashwa kuze kube yilapho kuvela isifo noma ubuthi obungamukeleki.

Umphumela oyinhloko wokusebenza ngempumelelo kuzo zombili izivivinyo kwaba ukusinda okuphelele (OS). Ukusinda okuphelele okumaphakathi eqenjini le-fruquintinib kwakuyizinyanga ezingu-7.4 (95% CI: 6.7, 8.2) uma kuqhathaniswa nezinyanga ezingu-4.8 (95% CI: 4.0, 5.8) eqenjini le-placebo. Isilinganiso sengozi sasingu-0.66 (95% CI: 0.55, 0.80) ngenani lika-p elingaphansi kuka-0.001. Ukusinda okuphelele okumaphakathi (OS) ocwaningweni lwe-FRESCO kwakuyizinyanga ezingu-9.3 (95% CI: 8.2, 10.5) kanye nezinyanga ezingu-6.6 (95% CI: 5.9, 8.1) emaqenjini ahlukene okwelapha. Isilinganiso sengozi (HR) sasingu-0.65 (95% CI: 0.51, 0.83) ngenani elibalulekile ngokwezibalo lika-p elingaphansi kuka-0.001.

Imiphumela emibi evamile (etholwe iziguli ezingamaphesenti angu-20 noma ngaphezulu) yayihlanganisa umfutho wegazi ophakeme, i-palmar-plantar erythrodysesthesia, i-proteinuria, i-dysphonia, ubuhlungu besisu, isifo sohudo, kanye ne-asthenia.

Umthamo ophakanyisiwe we-fruquintinib ngu-5 mg othathwa ngomlomo kanye ngosuku, ngokudla noma ngaphandle kokudla, ezinsukwini zokuqala ezingama-21 zomjikelezo wezinsuku ezingama-28 kuze kube yilapho isifo siqhubeka noma ubuthi obungabekezeleleki.

Buka imininingwane egcwele ye-fruquintinib.

Bhalisa ku-Newsletter yethu

Thola izibuyekezo futhi ungalokothi uphuthelwe ibhulogi evela kuCancerfax

Okuningi Okuzohlolwa

Ukuqonda i-BCMA: Ithagethi Yenguquko Ekulapheni Umdlavuza
Umdlavuza wegazi

Ukuqonda i-BCMA: Ithagethi Yenguquko Ekulapheni Umdlavuza

Isingeniso Emkhakheni oguqukayo njalo wokwelashwa kwe-oncological, ososayensi baphikelela befuna izinhloso ezingajwayelekile ezingakhulisa ukusebenza kokungenelela kuyilapho kunciphisa imiphumela engadingeki.

Dinga usizo? Ithimba lethu likulungele ukukusiza.

Sifisela ukululama okusheshayo kothandekayo wakho futhi oseduze.

Qala ingxoxo
Siku-inthanethi! Xoxa Nathi!
Skena ikhodi
Sawubona,

Siyakwamukela kuCancerFax!

ICancerFax iyinkundla yokuphayona ezinikele ekuxhumaniseni abantu ababhekene nomdlavuza oseqophelweni eliphezulu ngemithi yokwelapha yamangqamuzana efana ne-CAR T-Cell therapy, ukwelashwa kwe-TIL, nezivivinyo zomtholampilo emhlabeni wonke.

Sazise ukuthi yini esingakwenzela yona.

1) Ukwelashwa komdlavuza phesheya?
2) Ukwelashwa kwe-CAR T-Cell
3) Umuthi wokugomela umdlavuza
4) Ukubonisana ngevidiyo eku-inthanethi
5) Ukwelashwa kweProton