FDA Investigating Serious Risk Of Hematologic Malignancy Following Skysona (Elivaldogene Autotemcel)
FDA Investigating Serious Risk Of Hematologic Malignancy Following Skysona (Elivaldogene Autotemcel)
WARNING: HEMATOLOGIC MALIGNANCY Hematologic malignancy, including life-threatening cases of myelodysplastic syndrome, has occurred in patients treated with SKYSONA. Patients have been diagnosed between 14 months and 7.5 years after SKYSONA administration, and the cancers appear to be the result of the SKYSONA lentiviral vector, Lenti-D, integration in proto-oncogenes. Monitor patients closely for evidence of malignancy through complete blood counts at least every 6 months and through assessments for evidence for clonal expansion or predominance at least twice in the first year and annually thereafter; consider bone marrow evaluations as clinically indicated [see Warnings and Precautions (5.1)].
警告:血液系統惡性腫瘤 服用SKYSONA的患者中出現了包括有生命危險的骨髓增生異常綜合症在內的血液系統惡性腫瘤。患者在接受SKYSONA治療後14個月至7.5年之間被確診,這些癌症似乎是由SKYSONA慢病毒載體Lenti-D在原癌基因中整合所致。密切監測患者是否有惡性腫瘤的跡象,至少每6個月進行完整血細胞計數,並且在第一年至少兩次及以後每年考慮骨髓評估(根據臨床情況所需)[請參閱警告和注意事項(5.1)]。
譯文內容由第三人軟體翻譯。