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. 2020 Jan 1;10(4):1708–1718. doi: 10.7150/thno.38339

Table 2.

Changes in tumor infiltrating lymphocytes following ICI therapy in serial tumor tissues measured immunohistochemically

Setting Treatment Tumor type Number of patients Sampling time points Summary of findings Reference
Neoadjuvant 2 cycles nivolumab 3 mg/kg body weight NSCLC 21 Baseline and tumor resection after 4 weeks Major pathological response in 45% of resected tumors (80)
Neoadjuvant 2 cycles ipilimumab + nivolumab Melanoma 10 Baseline and tumor resection after 6 weeks Pathological response in 70% of biopsies (81)
Neoadjuvant 1 cycle pembrolizumab Melanoma 27 Baseline and tumor resection after 3 weeks Complete or major pathologic response in 30% of patients. Increase in CD8 positive T cell numbers compared to pre-treatment biopsy (82)
On-treatment biopsy CTLA-4 blockade and/or PD-1 blockade Melanoma 53 Baseline and early on treatment (after 2-3 doses) Increase in CD8+ T cells (83)
On-treatment biopsy Pembrolizumab Melanoma 46 - Baseline
- 20-60 days
- 80-120 days
- 120 days
Increase in CD8 T cell density (cells/mm2) in responders. Stable CD8 numbers in non-responders (84)
On-treatment biopsy Pembrolizumab Melanoma 53 Baseline and on treatment (median 74 days) Increase in T cell frequency. Increase in CD8+ effector memory T cells in responders. No changes in Treg frequencies (85)
On-treatment biopsy Anti-PD1 therapy Melanoma 13 Baseline and early on treatment (14 days) Significant expansion of CD8+ cells early during treatment. Higher CD8 T cell numbers were seen in responders (86)

Abbreviations: CD8: cluster of differentiation 8; CTLA-4: cytotoxic T lymphocyte antigen 4; NSCLC: non-small-cell lung carcinoma; PD-1, programmed cell death 1; Treg: regulatory T cell.