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Table 1 Studies Comparing Outcomes in Advanced Malignancy Patients on Treatment with Anti-Programmed Cell Death Protein 1 (PD-1) and Anti-Programmed Death-Ligand 1 (PD-L1) Antibodies

From: Immune-related adverse events and anti-tumor efficacy of immune checkpoint inhibitors

Study

Disease

Number of Patients

Checkpoint Inhibitor(s) Used

Survival Endpoints Between Patients With and Without IRAES

Response Endpoints Between Patients With and Without IRAEs

Grangeon et al. [18]

NSCLC

270

Anti-PD-1 and anti-PD-L1

OS (HR 0.29; 95% CI 0.18–0.46; p = .001), PFS (HR 0.42; 95% CI 0.32–0.57; p < .001)

ORR (22.9% vs 5.7%, p < .0001), DCR (76% vs 58%, p < .001)

Ricciuti et al. [34]

NSCLC

195

Nivolumab

OS (HR 0.33; 95% CI 0.23–0.47; p < .001), PFS (HR 0.41; 95% CI 0.3–0.57; p < .001)

ORR (43.5% vs 10%, p < .001), DCR (70.5% vs 18.1%, p < .0001)

Riudavets et al. [13]

NSCLC, UCC and melanoma

178

Nivolumab, pembrolizumab and atezolizumab

OS (37.3 vs 7.8 months, p < 0.0001), PFS (7.9 vs 2.6 months, p < 0.0001)

Not provided

Sato et al.a [19]

NSCLC

38

Nivolumab

PFS (HR 0.1; 95% CI .02–.37; p < .001)

ORR (63.6% vs 7.4%, p < .01)

Weber et al. [38]

Melanoma

576

Nivolumab

PFS (no significant differences between either group; HR or p value not provided)

ORR (48.6% vs 17.8%, p < .001)

Indini et al. [37]

Melanoma

173

Anti-PD-1

OS (HR 0.39; 95% CI 0.18–0.81; p = .007), PFS (HR 0.47; 95% CI 0.26–0.86; p = .016)

ORR (HR 1.95; 95% CI 0.91–4.15; p < 0.082), DCR (HR 1.98; 95% CI 1.07–3.67; p < 0.029)

Elias et al. [17]

RCC

90

Anti-PD-1

OS (HR 0.38; 95% CI 0.18–0.79; p = .01) and TTNT (HR 0.48; 95% CI 0.28–0.83; p = .008)

Not provided

Verzoni et al. [39]

RCC

389

Nivolumab

OS (HR .57; 95% CI .35–.93; p = .02)

Not provided

Maher et al. [20]

UCC

1747

Atezolizumab or pembrolizumab

OS (HR 0.53; 95% CI 0.43–0.66)

Not provided

Morales-Berera et al. [40]

UCC

52

Anti-PD-1 or anti-PD-L1

OS (21.91 vs 6.47 months, p = .004)

DCR (79% vs 36.3%, p = .002)

Das et al. [41]

GI

61

Anti-PD-1 monotherapy or in combination

OS (32.4 vs 8.5 months, p = .0036), PFS (32.4 vs 4.8 months, p = .0001)

Not provided

Masuda et al. [42]

Gastric

65

Nivolumab

OS (HR .17, p < .001), PFS (HR .11, p < .001)

Not provided

Foster et al. [43]

HNSCC

114

Anti PD-1

OS (12.5 vs 6.8 months, p = .0007), PFS (6.9 vs 2.1 months, p = .0004)

ORR (30.6% vs 12.3%, p = .02)

  1. Abbreviations: NSCLC non-small cell lung cancer, UCC urothelial cell carcinoma, RCC renal cell carcinoma, GI gastrointestinal, HNSCC head and neck squamous cell carcinoma, IRAEs immune related adverse events, OS overall survival, PFS progression-free survival, ORR overall response rate, DCR disease control rate, HR hazard ratio, CI confidence interval, TTNT time to next treatment, vs versus
  2. aProspective study