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. 2023 Jul 19;14(25):2567–2578. doi: 10.1111/1759-7714.15036

TABLE 1.

Patient characteristics.

Characteristics Total number of patients (n = 236)
Sex
Male/female 189/47
Median age at treatment (years) (range) 68 (24–82)
Performance status
0/1/2/3/4 82/138/15/1/0
Smoking history
Yes/no 209/27
Clinical stage at diagnosis
II/III/IV/postoperative recurrence 1/9/178/48
Histology
Adenocarcinoma/others 216/20
PD‐L1 tumor proportion score (%)
<1/1–49/≥50/unknown 77/75/57/27
Driver gene mutation/translocation
EGFR/ALK/others/wild‐type, negative, or unknown a 5/0/27/204
History of postoperative adjuvant chemotherapy
Yes/no 33/203
Intracranial metastases at initial treatment
Yes/no 58/178
Liver metastases at initial treatment
Yes/no 12/224
Bone metastases at initial treatment
Yes/no 88/148
Body mass index (kg/m2)
Median (range) 22.2 (13.3–36.5)
Prior radiotherapy b
Yes/no 58/178
Number of cycles of platinum+pemetrexed+pembrolizumab administered
Median 4
Range 1–6
Number of cycles of maintenance therapy administered c
Median 3
Range 0–51
Platinum agent
Cisplatin/carboplatin 46/190
Reason for discontinuation of platinum + pemetrexed + pembrolizumab administration d
Progressive disease 28
Adverse events 39
Worsening of performance status 6
Others 9
Steroid treatment for adverse events e
Yes/no 63/173
Laboratory data, median (range)
C‐reactive protein (mg/dL) 0.70 (0.01–21.0)
Albumin (g/dL) 3.7 (1.7–4.8)
Neutrophil (cells/μL) 4718.5 (1200–23 360)
Lymphocyte (cells/μL) 1361 (285–3610)
Continuing administration of maintenance therapy at data cutoff 23
a

Test results showed no known genetic abnormalities such as EGFR mutations and ALK fusion genes, or no known genetic abnormalities had been tested for.

b

Curative intent and palliative radiotherapy.

c

Including pemetrexed + pembrolizumab, pemetrexed, or pembrolizumab maintenance therapy.

d

Excluding maintenance therapy.

e

Excluding topical agents.