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Clinical course of patients with renal cell carcinoma or urothelial carcinoma who had stable disease as an initial response to a PD-1 or PD-L1 inhibitor

Authors
Hwang, InhwanPark, InkeunYoon, Shin-KyoLee, Jae Lyun
Issue Date
Aug-2022
Publisher
WILEY
Keywords
duration of stable disease; immune checkpoint inhibitors; renal cell carcinoma; urothelial cell carcinoma
Citation
Asia-Pacific Journal of Clinical Oncology, v.18, no.4, pp.371 - 377
Journal Title
Asia-Pacific Journal of Clinical Oncology
Volume
18
Number
4
Start Page
371
End Page
377
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/84985
DOI
10.1111/ajco.13601
ISSN
1743-7555
Abstract
Background: About 17%–34% of patients with non-prostatic genitourinary (GU) cancer had stable disease (SD) as their best response to programmed cell death protein 1/programmed death-ligand 1 (PD-1/PD-L1) inhibitors. However, most efficacy studies of PD-1/PD-L1 inhibitors are focused on the response and its durability. Little is known about patients' clinical outcomes with SD as their initial response to PD-1/PD-L1 inhibitors. Methods: We retrospectively reviewed the clinical outcomes of patients with renal cell carcinoma (RCC) (n = 102) and urothelial carcinoma (UC) (n = 101) treated with PD-1/PD-L1 inhibitors. The duration of SD (DoSD) was calculated for patients who had SD as their best response and was defined from the time of SD to radiologically confirmed progressive disease (PD) or death. Results: Fifty-five patients (27.1%) had SD as the initial response. Among them, 10 patients (18.2%) achieved a response on subsequent assessments. With a median follow-up duration of 15.2 months, the median DoSD was 8.5 months (range: 3.2–13.8), which was significantly different according to the disease; 9.4 months in RCC and 2.3 months in UC (p = 0.03). If the disease did not progress in 4 months (long SD subgroup), the DoSD (11.0 months) was comparable to the duration of response (12.9 months) in patients who achieved a complete or partial response to PD-1/PD-L1 inhibitors. In addition to the cancer type, the clinical factors associated with short DoSD were liver metastases (p = 0.003), neutrophil-lymphocyte ratio (NLR) > 4.0 (p = 0.001), and platelet-lymphocyte ratio (PLR) > 194 (p = 0.003). Conclusion: For RCC patients with SD to PD-1/PD-L1 inhibitors, if there are no liver metastases and NLR/PLR is below the certain level, they would have similar duration of disease control and survival benefit as those who achieve the response. © 2021 John Wiley & Sons Australia, Ltd.
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