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. 2022 Dec 9;29(10):1835–1854. doi: 10.1158/1078-0432.CCR-22-1922

Table 1.

Clinical efficacy of select TIL therapy trials in melanoma.

Trial No. of prior therapies, % Intervention/Pts, n/ disease stage Lymphodepletion/ IL2 regimen TIL preparation TIL product/ IL2 doses received Efficacy outcomes
Rosenberg et al. 1994 (127)
  • Surgery, 80%

  • IO, 43%

  • Chemotherapy, 20%

  • Radiotherapy, 10%

  • None, 3%

  • Hormonal therapy, 1%

  • TIL + IL2±Cy

  • 86

  • Metastatic disease

  • Lymphodepletion:

    • Cy: 25 mg/kg

  • IL2:

    • 720,000 IU/kg every 8 hr max 15 doses

  • Minced into 3- to 5-mm fragments and digested overnight in an enzyme medium

  • TIL:

    • >1011 cells in cycle 1 (85% of pts)

    • >2 × 1011 cells in cycle 1 (48% of pts)

  • ORR:

    • IL2 alone: 35% (n = 29)

    • IL2 + Cy: 35% (n = 57)

    • All: 34% (n = 86)

Schwartzentruber et al. 1994 (128)
  • Surgery, 95%

  • Chemotherapy, 29%

  • Radiation, 7%

  • Hormonal/non–IL2 IO, 67%

  • IL2-based therapy, 49%

  • TIL therapy, 14%

  • TIL + IL2 (±IFN-α) ±Cy

  • 43

  • Stage IV

  • Lymphodepletion:

    • Cy: 25 mg/kg

  • IL2:

    • 720,000 IU/kg IV every 8 hr OR 216,000 IU/kg and IFN-α: 3 × 106 U/m2 IV every 8 hr

  • Minced and enzymatically digested

  • Cells were cultured in IL2–containing media for 28 to 84 d

  • TIL (mean ± SEM):

    • Cycle 1: responders: 1.9 ±0.1×10−11; nonresponders: 1.5 ± 0.1×10−11

    • Cycle 1 + 2: responders: 3.2 ± 0.3×10−11; nonresponders: 2.4±0.2×10−11

  • IL2 doses (mean ± SEM):

    • Cycle 1: responders: 2.6 ±0.4 × 10−6 IU/kg; Cycle 1: nonresponders: 2.5 ±0.3 × 10−6 IU/kg

    • Cycle 1 + 2: responders: 5.8 ±0.9×10−6 IU/kg; nonresponders: 4.9 ± 0.5×10−6

  • ORR: 21%

Dudley et al. 2002 (23)
  • IL2, 100%

  • Chemotherapy, 62%

  • TIL+ Cy/Flu + IL2

  • 13

  • HLA-A2+ metastatic melanoma

  • Lymphodepletion:

    • Cy: 60 mg/kg for 2 d + Flu 25 mg/ m2 for 5 d

  • IL2:

    • 720,000 IU/kg every 8 hr until tolerable toxicity

  • Small (2 mm3) tumor fragments or enzymatically digested tumor tissue

  • TIL cultures screened for autologous tumor cell and HLA-A2+ reactivity

  • Expanded to ≥5×107 cells (3–6 weeks)

  • TIL (average, range):

    • 7.8×1010 (2.3×1010 – 13.7×1010)

  • IL2 (average, range):

    • 9 (5 – 12)

  • ORR: 46% (n = 6)

Dudley et al. 2010 (129)
  • IL2, 62%

  • Lymphodepletion±TBI + TIL + HD IL2

  • 56

  • M1a-M1c

  • Lymphodepletion:

    • Cohort 1: Cy 60 mg/kg for 2 d + Flu 25 mg/ m2 for 5 d (n = 33)

    • Cohort 2: Cy 60 mg/kg for 2 d + Flu 25 mg/ m2 for 5 d (n = 33) + TBI 3×2 Gy (n = 23)

  • CD8+ enriched young TILa

  • TILb (average± standard error):

    • Cohort 1: 47.7 ±3.3×109

    • Cohort 2: 43.1 ± 7.5×109

  • IL2:

    • Cohort 1: 6.3 ± 0.3

    • Cohort 2: 7.5 ± 0.5

  • ORR:

    • Cohort 1: 58%

    • Cohort 2: 48%

    • All: 54%

Rosenberg et al. 2011 (9)
  • Median = 2 (mean ± SEM = 2 ±0.2)

  • IL2, 83%

  • IFN, 56%

  • Chemotherapy, 43%

  • IL2+Chemotherapy, 40%

  • Anti–CTLA-4, 12%

  • IL2+anti–CTLA-4, 9%

  • IL2+anti–CTLA-4 + chemotherapy, 7%

  • None, 5%

  • Lymphodepletion±TBI + TIL + HD IL2

  • 93

  • M1a-M1c

  • Lymphodepletion:

    • Cohort 1: Cy 60 mg/kg for 2 d + Flu 25 mg/ m2 for 5 d (n = 43)

    • Cohort 2: Cy 60 mg/kg for 2 d + Flu 25 mg/ m2 for 5 d + TBI 2 Gy (n = 25)

    • Cohort 3: Cy 60 mg/kg for 2 d + Flu 25 mg/ m2 for 5 d +12 TBI (TBI 2 × 2 Gy/d for 3 d) (n = 25)

  • IL2:

    • 720,000 IU/kg every 8 hr until tolerable toxicity, max 15 doses

    • Cohort 2/3 received ≤2 × 106/kg of CD34+ HPSCs

  • Single-cell suspensions or 1–2 mm3 fragments in 24-well cultures plates

  • Lesion size >2 cm in diameter

  • TIL (mean ± SEM):

    • CR (n = 20): 6.5 ± 0.7 × 10−10

    • PR (n = 32): 6.1 ± 0.5 × 10−10

    • NR (n = 41): 5.5 ± 0.6 × 10−10

  • IL2 (mean ± SEM):

    • CR: 7.1 ± 0.4

    • PR: 7.7 ± 0.5

    • NR: 8.8 ± 0.4

  • ORR:

    • Cohort 1: 49% (n = 43); (CR, 12%)

    • Cohort 2: 52% (n = 25); (CR, 20%)

    • Cohort 3: 72% (n = 25); (CR, 40%)

    • All: 56% (n = 93)

  • 3-yr OS rate:

    • CR: 100%

    • PR: 31%

    • NR: 7%

    • All: 36%

  • 5-yr OS rate:

    • CR: 93%

    • PR: 21%

    • NR: 5%

    • All: 29%

Radvanyi et al. 2012 (130)
  • Chemotherapy, 29%

  • Biochemotherapy, 29%

  • IO, 39%

  • Unknown, 3%

  • Lymphodepletion + TIL + 2 cycles HD IL2

  • 31

  • Stage IIIc, IV

  • Lymphodepletion:

    • Cy 60 mg/kg for 2 d (on d −7 and −6) + Flu 25 mg/m2 for 5 d from d −5 to −1

  • IL2:

    • 1st dose: 720,000 IU/kg until tolerable toxicity, max 15 doses; 2nd dose: 21 d post TIL

  • 1 lesion used in most cases, in some cases two to three smaller nodules

  • 3 to 5 mm3 cut fragments; manual dissection; pre-REP TIL cryopreserved (5 wk), thawed, further expanded to post-REP TIL

  • Treatment: post-REP TIL

  • TIL (range):

    • 8 to 150×109

  • IL2:

    • 2 cycles (n = 28/31 pts)

  • mOS: NR

  • mPFS: 7.6 mo (95% CI, 4.1 mo -22.2 mo)

Besser et al. 2013 (38)
  • Previous therapy, 100%

  • IL2-based therapy, 95%

  • Ipilimumab therapy, 23%

  • Lymphodepletion + TIL + HD IL2

  • 80

  • Stage IV (M1a-M1b)

  • BRAFV600/E mutations (n = 34/80)

  • Lymphodepletion:

    • Cy 60 mg/kg for 2 d + Flu 25 mg/ m2 for 5 d

  • IL2:

    • 720,000 IU/kg until tolerable toxicity, max 15 doses

  • Fragmentation, enzymatic digestion, and cell remnants

  • Young-TIL Pre-REP cultures (2 wk), cryopreserved or expanded (14 d)

  • Treatment: young TIL (n = 57)

  • TIL (total cell number, n = 57): 52 ± 24 × 109

  • ORR:

    • 40% (n = 57); (CR, 6%; PR, 23%)

    • 29% (n = 80); (CR, 9%; PR, 32%)

  • Treated pts (n = 57)

    • mOS: 15.2 mo

    • mPFS: 4 mo

  • 1-yr PFS rate: 42%

  • 1-yr OS rate: 50%

  • 2-yr OS rate: 45%

  • 3-yr OS rate: 42%

Anderson et al. 2016 (25)
  • IL2-based, 96%

  • Ipilimumab-based, 80%

  • Responders: median 2 (range, 1–4)

  • Nonresponders: median 2 (range, 2–4)

  • Lymphodepletion + TIL + LD IL2

  • 25

  • Stage IIIc, IV

  • Lymphodepletion:

    • Cy 60 mg/kg for 2 d (d −7 and −6) + Flu 25 mg/m2 for 5d (d −5 to −1)

  • IL2:

    • Decrescendo regimen (18 MIU/m2 for 6 hr, 18 MIU/ m2 for 12 hr, 18 MIU/ m2 for 24 hr followed by 4.5 MIU/ m2 for another 3×24 hr) (prescheduled IL2 dose was reduced by 25%–50% in 4 pts)

  • Lesions ≤1 cm3 were surgically resected and cut into 2 to 3 mm3 fragments

  • Pre-REP/ young TIL in 21 d (range, 13–36) were cryopreserved or entered REP

  • TIL (median):

    • 98 × 109 (range 61–20 × 109)

  • IL2 (median):

    • 112 MIU dose

  • ORR: 42% (n = 25)

  • mPFS: All: 3.9 mo

  • mOS: All: 21.8 mo

  • 1-yr OS rate: 72%

  • 3-yr OS rate: 40.8%

Goff et al. 2016 (24)
  • None, 26%

  • HD IL2, 29%

  • Anti–CTLA-4, 31%

  • Anti–PD-1, 3%

  • Anti–CTLA-4 and anti–PD-1, 8%

  • Adjuvant (IFNα, vaccine, etc.), 38%

  • Chemotherapy, 11%

  • BRAF and/or MEK inhibitor, 9%

  • Other (including biochemotherapy), 10%

  • NMA-lymphodepletion ±TBI + TIL + HD IL2

  • 101c

  • Advanced disease (76%, M1c)

  • Lymphodepletion:

    • Arm 1: NMA, Cy 60 mg/kg for 2 d + Flu 25 mg/m2 for 5 d

    • Arm 2: Cy 60 mg/kg for 2 d + Flu 25 mg/m2 for 5 d + TBI 2 Gy 2×/d (total of 1200 TBI)

  • IL2:

    • 720,000 IU/kg every 8 hr until tolerable

  • Cohort 2 received ≤2×106/kg of CD34+ HPSCs

  • Single fragments of 2 to 3 mm2 were enzymatically digested and cryopreserved

  • Autologous reactive or actively growing cells were cryopreserved and/or selected for REP

  • IL2 median (range):

    • Arm 1: 6 (4–7)

    • Arm 2: 5 (3.3–6)

  • ORR: 54% (n = 54)

    • Arm 1: 45% (n = 23); (CR, 24%; PR, 22%)

    • Arm 2: 62% (n = 31); (CR, 24%; PR, 38%)

  • mPFS

    • Arm 1: 7.5 mo

    • Arm 2: 9.6 mo

  • mOS

    • Arm 1: 36.6 mo

    • Arm 2: 38.2 mo

van den Berg et al. 2020 (26)
  • Chemotherapy, 70%

  • Anti–CTLA-4, 100%

  • Adjuvant (IFNα, vaccine, etc.), 40%

  • BRAF and/or MEK inhibitor, 40%

  • NMA-lymphodepletion + TIL + HD IL2

  • 10

  • Stage IIIc/ IV

  • Lymphodepletion:

    • Cy 60 mg/kg for 2 d + Flu 25 mg/ m2 for 5 d

  • IL2:

    • 600,000 IU/kg every 8 hr until tolerable toxicity, max 15 doses

  • Enzymatic digestion

  • Growth 2–4 weeks to reach ≥1×108 cells followed by cryopreservation or REP

  • TILs harvested additional 14 days after growth

  • TIL (range):

    • 1.7 – 19.6 × 1010

  • IL2 median (range):

    • 3.5 (1–9)

  • ORR: 50% (n = 5)

    • CR, 20%

    • PR, 30%

Sarnaik et al. 2021 (12)
  • Mean = 3.3 (range, 1–9)

  • Anti–PD-1 or PD-L1, 100%

  • Anti–CTLA-4, 80%

  • Anti–PD-1+ CTLA-4, 52%

  • BRAF ± MEK, 88%

  • IL2, 11%

  • Surgery, 99%

  • Radiotherapy, 52%

  • Lymphodepletion + TIL + HD IL2

  • 66

  • Stage IIIc, IV

  • Lymphodepletion:

    • Cy 60 mg/kg for 2 d + Flu 25 mg/m2 for 5 d

  • IL2:

    • 600,000 IU/kg every 8 to 12 hr for up to 6 doses, starting within 3 to 24 hr after TIL infusion

  • At least one resectable lesion (or aggregate of lesions) measuring a minimum of 1.5 cm in diameter postresection

  • Mean target lesion diameter = 106 mm

  • Centralized 22-d process and cryopreserved product

  • TIL administered:

    • Total: >1 × 109 – <150 × 109

    • Mean: 27.3 × 109 (range, 1.2 × 109–99.5 × 109)

  • IL2:

    • Median 5.5 (range 1–6)

  • ORR: 36% (n = 24)

    • (CR, n = 2; PR, n = 22)

  • DCR: 80% (n = 53)

  • mOS: 17.4 mo (95% CI, 11.0-Not reached)

  • 1-yr OS rate: 58% (95% CI, 45%-69%)

Seitter et al. 2021 (10)
  • ≥1 prior systemic therapy, 83%

  • Anti–CTLA-4, 30%

  • Anti–PD-1+, 12%

  • Anti–PD-1+ CTLA-4, 4%

  • BRAF±MEK, 8%

  • IL2, 46%

  • Lymphodepletion + TIL + HD IL2

  • 226

  • Metastatic melanoma

  • Lymphodepletion:

    • Cy 60 mg/kg for 2 d + Flu 25 mg/ m2 for 5 d

  • IL2:

    • 720,000 IU/kg every 8 hr until tolerable

  • Multiple fragments of 2 to 3 mm2 placed into a single well of a 24-well tissue culture plate, supplemented with media with HD IL2 followed by REP or cryopreserved

  • TIL administered:

    • Maximum: 2 × 1011

  • IL2:

    • Median 6 (range 5–8)

  • ORR: 51% (n = 116)

    • (CR, n = 49; PR, n = 67)

  • mOS: 20.6 mo (95% CI, 15.2–29.9)

  • 3-yr OS rate: 41%

  • 5-yr OS rate: 35%

  • 10-yr OS rate: 32%

Levi et al. 2022 (33)
  • Anti–PD-1+, 38%

  • Anti–CTLA-4, 31%

  • Anti–PD-1+ CTLA-4, 93%

  • BRAF±MEK, 13%

  • HD IL2, 31%

  • IFNα, 30%

  • Chemotherapy, 14%

  • Lymphodepletion ± TBI + TIL + HD IL2 ± pembrolizumab

  • 181

  • Metastatic melanoma

  • Lymphodepletion:

    • Arm 1: Cy 60 mg/kg for 2 d + Flu 25 mg/m2 for 5 d

    • Arm 2: Cy 60 mg/kg for 2 d + Flu 25 mg/m2 for 5 d + 1,200 TBI cGy for 3 d

    • Arm 3: Cy 60 mg/kg for 2 d + Flu 25 mg/m2 for 5 d + 2 mg/kg pembrolizumab every 3 weeks for total of 4 doses

  • IL2:

    • 720,000 IU/kg every 8 hr until tolerable

  • At least one resectable lesion measuring ≥1 cm

  • REP with irradiated PBMC feeder cells, anti-CD3 antibody and IL2

  • TIL administered:

    • Total not reported

  • IL2:

    • Median not reported

  • ORR:

    • Anti–PD-1 naïve: 55% (CR, 51%)

    • Prior anti–PD-1 therapy: 26% (CR, 8%)

Haanen et al. 2022 (8)
  • None, 11%

  • Anti–PD-1, 86%

  • Lymphodepletion + TIL + HD IL2 OR ipilimumab

  • 168 (84 per arm)

  • Unresectable stage IIIc to IV melanoma

  • Lymphodepletion:

    • Cy 60 mg/kg/d for 2 d + Flu 25 mg/m2/d for 5 d

  • IL2:

    • 600,000 IU/kg every 8 hr

  • Tumor digested and/or fragmentated for initial outgrowth

  • REP with anti-CD3 antibody, feeder cells, and IL2

  • TIL administered:

    • Total: 5×109 – 2×1011

  • IL2:

    • Median not reported

  • ORR:

    • TIL: 49% (CR, 20%)

    • Ipi: 21% (CR, 7%)

  • mPFS:

    • TIL: 7.2 mo

    • Ipi: 3.1 mo

  • mOS:

    • TIL: 25.8 mo

    • Ipi: 18.9 mo

  • 6-mo PFS rate:

    • TIL: 53%

    • Ipi: 21%

  • 2-yr OS rate:

    • TIL: 54%

    • Ipi: 44%

Abbreviations: BRAF, B-Raf proto-oncogene, serine/threonine kinase; CD, cluster of differentiation; CR, complete response; Cy, cyclophosphamide; d, day; Flu, fludarabine; HD, high-dose; hr, hour; IO, immunotherapy; LD, low-dose; MEK, mitogen-activated protein kinase kinase; mo, months; NE, not estimable; NR, nonresponder; OS, overall survival; s.c., subcutaneous; PBMC, peripheral blood mononuclear cell; PFS, progression-free survival; PR, partial response; pts, patients; RFS, relapse-free survival; TBI, total body irradiation; wk, week, yr, year.

aIn the cohorts treated in this report, there was no difference between the age of CD8+ enriched young TIL cultures for responding and nonresponding patients.

bThree additional patients received cryopreserved TIL from prior resections.

cOf 101 patients randomly assigned to cohorts 1 or 2, all completed their planned treatment course except two patients in cohort 2 (TBI arm), whose treatment was aborted for progressive disease.