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. 2020 Sep 28;11(11):3317–3325. doi: 10.1111/1759-7714.13675

Table 2.

Chemotherapy regimens for patients with non‐small cell lung cancer (n = 14)

Patient First Second Third Fourth AE‐IPF
1 CBDCA + nab‐PTX S‐1
2 CBDCA + nab‐PTX CBDCA + S‐1 VNR S‐1 (rechallenge) +
3 CBDCA + nab‐PTX +
4 CBDCA + nab‐PTX
5 CBDCA + nab‐PTX S‐1 Pembrolizumab
6 CBDCA + nab‐PTX
7 CBDCA + nab‐PTX VNR S‐1
8 CBDCA + nab‐PTX S‐1 VNR +
9 CBDCA + S‐1 CBDCA + nab‐PTX S‐1 (rechallenge)
10 CBDCA + S‐1 CBDCA + nab‐PTX +
11 CBDCA + S‐1 CBDCA + nab‐PTX
12 CBDCA + S‐1 Pembrolizumab nab‐PTX
13 CBDCA + S‐1 Nivolumab CBDCA + nab‐PTX
14 CBDCA + S‐1 nab‐PTX Pembrolizumab

Treatment regimens discontinued due to adverse reactions other than AE‐IPF.

Treatment regimens induced chemotherapy‐associated AE‐IPF.

+ and −, Presence and absence of AE‐IPF until death, respectively.

CBDCA, carboplatin; AE‐IPF, acute exacerbation of idiopathic pulmonary fibrosis; nab‐PTX, nanoparticle albumin‐bound PTX; PTX, paclitaxel; VNR, vinorelbine.