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. 2020 May 13;9(5):1458. doi: 10.3390/jcm9051458

Table 1.

Characteristics of included studies.

Author/
Year
Type of Study
Of Patients (Disease)
Treatment Received (%) Median Age (Years) Ab%
/Timing
Median Duration (Weeks)/n° of AB Courses/pts Med
FUP
(mos)
Type of Analysis Covariates
of MVA
for OS
Quality
(NOS Score)
Abu-Sbeih/
2019
retrospective 826 (melanoma n = 347; hematologic n = 116; other n = 363) anti-PD(L)1 (51.6), anti-CTLA4 (32), combo (16.5) 62 68.9
/before or after start (47.5%), both (52.5%)
NR/NR NR MVA ICI type,
Stage IV cancer, IMDC, anaerobic AB use
6
Ahmed/
2018
retrospective 60 (NSCLC n = 34; other n = 26) anti-PD1 (81.7), anti-PDL1 (5),
ICI + CT (13.3)
59 28
/2w before and/or after start
1–2 NR MVA broad spectrum AB use, age 5
Derosa/
2018
retrospective 360 (RCC n = 121, NSCLC n = 239) RCC: anti-PD(L)1 (88), anti-PD(L)1 + anti-CTLA4 (8), anti-PD(L)1 + BEVA (4)
NSCLC: anti-PD(L)1 (86), combo (14)
64 21.5
/1 mos before start
NR/NR NR MVA RCC: ab 30–0 days/no AB IMDC risk, tumour burden
NSCLC: ab 30–0 days/no AB, PS, clinical trial Y/N, prior regimens >/<3
5
Elkrief/
2019
retrospective 59 (melanoma) * NIVO/PEMBRO/IPI (100) 64.5 13.5°
/1 month before
0.9/NR NR MVA age, PS, gender, AB use, LDH, BRAF, line of tx, type of ICI 5
Galli/
2019
retrospective 157 (NSCLC) anti-PD(L)1 (95.6), anti-CTLA4 o combo (4.4) 66.7 17.2
/during ICI period
1/NR 28.6 MVA high AB /immunotherapy exposure ratio through entire ICI period 8
Guo/
2019
retrospective 49 (oesophageal) anti-PD(L1) alone (61), combo (39) 56.7 43/2 mos before or 1 month after 1.42/NR 16.4 MVA PS, treatment, n° of metastatic sites, NLR, antibiotic use 7
Hakozaki/
2019
retrospective 90 (NSCLC) NIVO (100) 68 14.4/1 month before start >1 (84.6%)/ NR MVA driver mutations 6
Huemer/
2018
retrospective 30 (NSCLC) NIVO (83), PEMBRO (17) NR 37/1 month before/after start NR/NR NR MVA sex, antibiotic use, ICI, EGFR/ALK mutations, line of tx, PDL1 status, immune-related adverse events 5
Huemer/
2019
retrospective 142 (NSCLC) NIVO, PEMBRO or ATEZO (100) 66 44/1 months before or after start NR/NR 13.3 UVA NR 7
Kaderbhai/
2017
retrospective 74 (NSCLC) NIVO (100) 67.5 20.3/3 months before or concurrent 1/NR NR UVA (PFS) NR 5
Krief/
2019
prospective cohort 72 (NSCLC) NIVO (100) 68.8 42/2 months before or 1 month after start 1.35/1.7 16.6 MVA AB use; KRAS mutations, gemmatimonadaceae on blood microbiome at baseline 7
Pinato/
2019
prospective cohort 196 (NSCLC n = 118; melanoma n = 38; RCC n = 11; other n = 26) anti-PD(L)1 (96) 68 29/1 month before or concurrent NR/NR NR MVA response to ICI, AB 0–30 days before ICI 6
Sen/
2018
retrospective 172 (NSCLC n = 21; RCC n = 25; melanoma n = 16; sarcoma n = 16; other n = 94) anti-CTLA4 (61), anti-PD1 (39) 60 33/during and up to 2 mos before NR/NR NR UVA NR 5
Tinsley/
2019
retrospective 291 (melanoma n = 179, RCC n = 48, NSCLC n = 69) NR 66 32/2w before up to 6w after start NR/NR NR MVA AB use, comorbidities, metastatic sites > 3, PS > 0 6
Zhao/
2019
retrospective 109 (NSCLC) anti-PD1 (52.3), anti-PD1 + CT (30.3), anti-PD1 + antiangiogenic (17.4) 62 18.3/1 mos before or after start NR/NR NR MVA AB use, PS 6

* only immunotherapy without chemotherapy; °: all patients; AB: antibiotic; mos: months; RCC: renal cell carcinoma; NSCLC: non-small-cell lung cancer; PD1: programmed death 1; PDL1: programmed death-ligand 1; ICI: immune checkpoint inhibitors; CT: chemotherapy; CTLA4: Cytotoxic T-lymphocyte antigen 4; BEVA: bevacizumab; NIVO: nivolumab; PEMBRO: pembrolizumab; IPI: ipilimumab; ATEZO: atezolizumab; MVA: multivariate analysis; UVA: univariate analysis; PFS: progression-free survival; IMDC: international metastatic RCC database consortium; PS ECOG: performance status; tx: therapy; NLR: neutrophil to lymphocyte ratio; NR: not reported; AB: antibiotics; combo: combination of two immune checkpoint inhibitors.