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. 2020 Dec 26;38(2):1245–1262. doi: 10.1007/s12325-020-01590-w

Table 2.

Treatment history prior to talimogene laherparepvec administration

Treatment history before initiating T-VEC Austria, Germany, UK (n = 35) Netherlands (n = 31) Total (N = 66)
n (%) n (%) n (%)
Surgery, N (%) 35 (100) 31 (100) 66 (100)
 Type of surgery, n (%)
  Recorded resection of recurrent disease 17 (48.6) 21 (67.7) 38 (57.6)
  Sentinel biopsy 18 (51.4) 9 (29.0) 27 (40.9)
  Lymphadenectomy 17 (48.6) 7 (22.6) 24 (36.4)
 No. of resections for recurrent disease per patient, median (IQR; range) 3.0 (1, 4; 1–11) 1.0 (1, 3; 1–10) 2.0 (1, 4; 1–11)
 Months from most recent resection for recurrent disease to initiating T-VEC, median (IQR; range) 10.0 (4, 22; 2–77) 6.2 (4, 11; 2–45) 7.4 (4, 15; 2–77)
Adjuvant therapy, N (%) 12 (34.3) 0 12 (18.2)
 Local (intralesional therapy injection of IL-2 or IFNα) 3 (25.0) 0 3 (25.0)
 Systemic (IFNα) 12 (100) 0 12 (100)
Locoregional therapy, N (%) 17 (48.6) 12 (38.7) 29 (43.9)
 Radiation therapy 14 (82.4) 1 (8.3) 15 (51.7)
 Local ablation therapy 1 (5.9)a 5 (41.7) 6 (20.7)
 Electrochemotherapy 4 (23.5)a 0 4 (13.8)
 Isolated limb perfusion 2 (11.8)a 9 (75.0) 11 (37.9)
 Intralesional therapy injection of IL-2 or IFNα 3 (17.6)a 0 3 (10.3)
 Topical imiquimod 1 (5.9)b 0 1 (3.4)
 Other 1 (5.9)c 0 1 (3.4)
Systemic therapy, N (%) 21 (60.0) 2 (6.5) 23 (34.8)
 IFNα 12 (57.1) 0 12 (52.2)
 Pembrolizumab 8 (38.1) 2 (100) 10 (43.5)
 Ipilimumab 8 (38.1) 0 8 (34.8)
 Chemotherapyd 7 (33.3) 0 7 (30.4)
 IL-2 3 (14.3) 0 3 (13.0)
 Nivolumab 3 (14.3) 0 3 (13.0)
 Dabrafenib 0 1 (50.0) 1 (1.5)
 Imatinib 1 (4.8) 0 1 (4.3)
 Ipilimumab/nivolumab 1 (4.8) 0 1 (4.3)
 Trametinib/dabrafenib 1 (4.8) 0 1 (4.3)

IFN interferon, IL interleukin, IQR interquartile range, T-VEC talimogene laherparepvec

aPrior treatment only in Germany

bPrior treatment only in Austria

cOther local therapy was “Chemoperfusion, left leg with melphalan” for a patient in Austria

dExamples of chemotherapies given included dacarbazine, temozolomide and taxanes