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. 2021 Sep 29;12:718418. doi: 10.3389/fendo.2021.718418

Table 3.

Summarised course of disease in 6 patients with sporadic medullary thyroid carcinoma (sMTC) and in 1 patient with MEN2a.

Patient Period elapsed after MTC diagnosis [months] Tumor burden/Progress according to RECIST ECOG status at therapy initiation Therapy duration[months] Reason to discontinue vandetanib Therapy-pause duration until progression [months] CDT at progression or end of observation Intervention Status
1 252 Moderate / yes 0 73 Duration vs. concern about toxicity Ongoing
(47 months, SD)
> 2 SD
2 76 High / no 0 58 Duration vs. concern about toxicity Ongoing
(61 months, SD)
> 2 SD
3 102 High / yes 0 7 Patient´s will, AE 9 (PD) < 2 Re-start declined Dead 6 months after PD; 15 months after TKI pausation
4 47 Moderate / yes 0 87 Duration vs. concern about toxicity 45 (PD) < 2 Re-start vandetanib SD in latest scan 29 months after re-start of TKI
5 87 High / yes 0 12 AE 52 (PD) >2, but CEA-DT critical (2.1 yrs) Re-start vandetanib, SD in latest scan 12 months after re-start of TKI
6 54 High / yes 1 38 AE 5 (PD) < 2 Re-start declined Dead 2 months after PD; 7 months after TKI pausation
7 31 High / yes 0 36 AE 45 (PD) < 2 Enrollment in clinical trial SD

Indication for TKI therapy with vandetanib. Tumour burden (high: progressive distant metastasis; moderate: progressive locoregional metastasis), therapy duration, reason to discontinue therapy, therapy pause duration until progression or end of observation in 04/2021 along with CDT and current status are shown. SD, stable disease; PD, progressive disease; CDT, calcitonin doubling time; CEA-DT, carcinoembrionic antigen doubling time; AE, Adverse event.