Although the association of both RFC2 and RFC4 protein expression with OS showed borderline significance, application of the prognostic risk model to our center’s cohort demonstrated that the high-risk group had a significantly shorter OS than the low-risk group ( P = 0.003).
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A DLBCL Prognostic model superior to the IPI score: Mechanistic study and clinical validation based on RFC2- and RFC4-mediated DNA damage repair.
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