Early C-reactive protein kinetics predict survival of patients with advanced urothelial cancer treated with pembrolizumab.


Journal

Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 14 03 2020
accepted: 20 08 2020
pubmed: 3 9 2020
medline: 9 3 2021
entrez: 3 9 2020
Statut: ppublish

Résumé

To assess the prognostic and predictive ability of early C-reactive protein (CRP) kinetics, dynamic changes in CRP levels, in patients with advanced urothelial cancer treated with pembrolizumab. We retrospectively evaluated 97 patients with advanced urothelial cancer treated with pembrolizumab in second-line or later settings. Patients were divided into three early CRP kinetics groups: non-elevated (baseline CRP < 5 mg/L), responder (baseline CRP ≥ 5 mg/L and CRP decreased below baseline at least once within 30 days), and non-responder (baseline CRP ≥ 5 mg/L and CRP never decreased to baseline within 30 days). Association between early CRP kinetics and pembrolizumab efficacy including objective response rate (ORR), disease control rate (DCR), and overall survival (OS) were evaluated. Based on early CRP kinetics, 40, 27, and 30 patients were classified as non-elevated, responder, and non-responder, respectively. ORR and DCR were 33% and 60% in non-elevated, 30% and 48% in responder, and 17% and 40% in non-responder; without a statistically significant difference. OS was significantly different among the non-elevated, responder, and non-responder groups (p < 0.01), with 1-year survival rates of 69%, 61%, and 31%, respectively. Early CRP kinetics could discriminate the OS of patients without objective response. Non-responder was an independent predictor for OS (HR 3.65, p < 0.01), as well as liver metastasis and ECOG PS ≥ 2. Early CRP kinetics is associated with survival of advanced urothelial cancer patients treated with pembrolizumab and could be a potential biomarker for clinical benefit from immune checkpoint inhibitors.

Identifiants

pubmed: 32876736
doi: 10.1007/s00262-020-02709-2
pii: 10.1007/s00262-020-02709-2
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
Biomarkers 0
C-Reactive Protein 9007-41-4
pembrolizumab DPT0O3T46P

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

657-665

Références

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Auteurs

Toshiki Kijima (T)

Department of Urology, Tokyo Medical and Dental University Graduate School, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.

Hina Yamamoto (H)

Department of Urology, Tokyo Medical and Dental University Graduate School, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.

Kazutaka Saito (K)

Department of Urology, Tokyo Medical and Dental University Graduate School, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan. kz-saito.uro@tmd.ac.jp.

Shota Kusuhara (S)

Department of Breast and Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Soichiro Yoshida (S)

Department of Urology, Tokyo Medical and Dental University Graduate School, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.

Minato Yokoyama (M)

Department of Urology, Tokyo Medical and Dental University Graduate School, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.

Yoh Matsuoka (Y)

Department of Urology, Tokyo Medical and Dental University Graduate School, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.

Noboru Numao (N)

Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Yasuyuki Sakai (Y)

Department of Urology, Saitama Cancer Center, Saitama, Japan.

Nobuaki Matsubara (N)

Department of Breast and Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Takeshi Yuasa (T)

Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Hitoshi Masuda (H)

Department of Urology, National Cancer Center Hospital East, Kashiwa, Japan.

Junji Yonese (J)

Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Yukio Kageyama (Y)

Department of Urology, Saitama Cancer Center, Saitama, Japan.

Yasuhisa Fujii (Y)

Department of Urology, Tokyo Medical and Dental University Graduate School, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.

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