Method for evaluating side-effect onset risk in anticancer drug treatment, including detecting muc4 gene polymorphism
A technology of gene polymorphism and determination method, which is applied in the field of determining the risk of occurrence of side effects of anticancer drug therapy including the step of detecting MUC4 gene polymorphism, and can solve problems such as death
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Embodiment 1
[0089]
[0090] Samples from 262 patients with drug-induced lung injury and 180 patients with interstitial lung disease, that is, a total of 442 patients, were collected from 30 auxiliary medical institutions across the country.
[0091] Among them, 180 patients with interstitial lung disease included 141 patients with acute exacerbation of IPF.
[0092] In addition, 262 patients with drug-induced lung injury included the following cases.
[0093] 49 patients with interstitial lung disease (ILD) caused by Iressa or Tarceva (hereinafter referred to as "Iressa ILD + Tarceva ILD"),
[0094] 3 patients with interstitial lung disease (ILD) (hereinafter referred to as XALCORI ILD) caused by XALCORI,
[0095] 38 patients with interstitial lung disease (ILD) caused by Taxotere (hereinafter referred to as Taxotere ILD)
[0096]
[0097] Among the above 442 cases, patient data + patient images were collected for 279 cases, and the diagnosis was confirmed. Among them, centering on...
Embodiment 2
[0100] (Example 2)
Embodiment 2-1
[0101] (Example 2-1)
[0102] For all the polymorphisms of 180215 mentioned above, the correlation analysis was carried out between 36 "Iressa ILD+Tarceva ILD" patients and 70 general Japanese. The result is as figure 1 shown. Bonferroni correction was performed, and a P value of 0.001 / 180215 or less was considered significant.
[0103] We believe, figure 1 In , isolated spots may also be an artifact caused by differences in the exon capture efficiency of each kit. Furthermore, we argue that points are aggregated into steeple-like parts contained in points (e.g., figure 1 The positions indicated by the middle arrows) indicate that in broad chromosomal regions, there is a difference in the frequency of polymorphisms between the two groups, showing a high probability of a true association.
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