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. 2022 Sep 23;6(24):6151–6161. doi: 10.1182/bloodadvances.2022008376

Table 2.

Interest in CHIP testing for patient in an introductory vignette at baseline, after disclosure of population-based risks, followed by CHIP-related risks, and then potential management strategies

Interest in CHIP testing following presentation of... Definitely not have the test, n (%) Probably not have the test, n (%) Probably have the test, n (%) Definitely have the test n (%) Not available, n (%) Change in testing preference compared with Switch from inclined to disinclined, n (%) Switch from disinclined to inclined, n (%) P value
Risks
 (1) Vignette alone 4 (0.8) 42 (8.0) 190 (36.0) 270 (51.1) 22 (4.2)
 (2) CHIP-independent, population-based risks for BC recurrence, hematologic malignancy, heart disease 12 (2.3) 87 (16.5) 195 (36.9) 210 (39.8) 24 (4.6) Vignette alone (1 vs 2) 56/504 (11.1) 3/504 (0.6) <.001
 (3) Increased CHIP-associated risks 7 (1.3) 47 (8.9) 171 (32.4) 278 (52.7) 25 (4.7) CHIP-independent population-based risks for BC recurrence, hematologic malignancy, and heart disease (2 vs 3) 7/503 (1.4) 51/503 (10.1) <.001
Actionability
 (4) Current management strategy 20 (3.8) 67 (12.7) 181 (34.3) 234 (44.3) 26 (4.9)
 (5) CHIP clinic 13 (2.5) 44 (8.3) 190 (36.0) 255 (48.3) 26 (4.9) Current management strategy (4 vs 5) 6/502 (1.2) 36/502 (7.2) <.001
 (6) Hypothetical treatment for CHIP 4 (0.8) 13 (2.5) 140 (26.5) 345 (65.3) 26 (4.9) Current management strategy (4 vs 6) 1/502 (0.2) 71/502 (14.1) <.001

CHIP testing inclination for self-dichotomized as inclined (definitely test or probably test) or disinclined (definitely not test or probably not test).