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. 2024 Jan 20;11(3):336–346. doi: 10.1093/nop/npae002

Table 2.

Patients Enrolled in the Feasibility Study

Pat No. Gender Age (years) Diagnosis Time since initial diagnosis (months) Molecular target Targeted therapy Time period targeted therapy (months) Number of prior targeted therapies (months) Initial ECOG Initial KPS Months TRACE app used End of study reached (usage app ≥ 6 months)
01 Female 57 Gallbladder carcinoma 26.1 FGFR2— KIIAA1598 FGFR inhibitor (Pemigatinib) 2 0 0 90 7.2 Yes
02 Female 34 Spinal ependymoma, CNS WHO grade 3 9.6 NF2 mTOR inhibitor (Everolimus) ONG 0 2 70 5.1** Yes
03 Female 61 Melanoma 72.5 CDKN2A, CDK4, CDK6, CCND2 CDK4/6 Inhibitor (Palbociclib) 1 1 (4) 1 80 11.9 Yes
04 Male 33 Diffuse midline glioma, CNS WHO grade 4 30.1 NF1 MEK inhibitor (Trametinib) ONG 1 (7.1) 1 90 7.0 Yes
05 Female 48 High-grade astrocytoma with piloid features 16.7 NF1 MEK inhibitor (Trametinib, Selumetinib) ONG 1 (6.5) 2 60 8.1 Yes
06 Male 33 Glioblastoma, IDH wildtype, CNS WHO grade 4 90.6 EGFR Tyrosine kinase inhibitor (Afatinib) 1 0 2 60 1.1 No, due to disease progression
07 Female 61 Gallbladder carcinoma 30.6 FGFR2—BICC1 FGFR inhibitor (Pemigatinib, Lenvatinib) ONG 1 (16.7) 1 80 13.3 Yes
08 Female 34 Pineal parenchymal tumor of intermediate differentiation, CNS WHO grade 2 273.3 DICER1 Nortiptyllin/
Gemcitabine
2 0 1 70 1.1 No, due to disease pro-gression
09 Male 28 Astrocytoma, IDH-mutant, CNS WHO grade 2 73 IDH1 IDH inhibitor (Ivosidenib) 4.6 0 1 80 5.3** Yes
10 Female 70 Gallbladder carcinoma 42.4 FGFR2—RBFOX2 FGFR inhibitor (Pemigatinib) ONG 0 1 80 7.2 Yes
11 Male 55 Meningioma, CNS WHO grade 2 209 NF2 mTOR (Everolimus) ONG 0 1 70 2.6 No, due to clinical deterioration1
12 Female 32 Papillary tumor of the pineal region WHO grade 2 48.4 NF2, PTEN mTOR inhibitor (Everolimus) ONG 0 0 90 6.3 Yes
13 Female 67 Oligodendroglioma, CNS WHO grade 2 130.8 IDH1 IDH inhibitor (Ivosidenib) n/a 0 2 60 0 Disease pro-gression
14 Male 59 Meningioma, CNS WHO grade 2 92.2 NF2 mTOR inhibitor (Everolimus) n/a 0 1 80 0 No longer interested

1The caregiver of the patient was interviewed.

Gray-shaded fields indicate patients (2) who gave informed consent to the study but did not start using the app.

Abbreviations: KPS = Karnofsky Performance Status, ONG = ongoing.

**The patient started the app in July 2022, due to data cut-off in 12/2022, the 6 months were not reached.