Hyperprogressive Disease in Patients With Urothelial Carcinoma or Renal Cell Carcinoma Treated With PD-1/PD-L1 Inhibitors

被引:33
|
作者
Hwang, Inhwan [1 ]
Park, Inkeun [2 ]
Yoon, Shin-kyo [1 ]
Lee, Jae Lyun [1 ]
机构
[1] Univ Ulsan, Asan Med Ctr, Dept Oncol, Coll Med, 88 Olymp Ro 43 Gil, Seoul 05505, South Korea
[2] Gachon Univ, Gil Hosp, Dept Internal Med, Div Med Oncol,Sch Med, Incheon, South Korea
关键词
Hyperprogression; Immune checkpoint inhibitors; Predictive factors; Renal cell carcinoma; Urothelial carcinoma; CISPLATIN-INELIGIBLE PATIENTS; SINGLE-ARM; MULTICENTER; PEMBROLIZUMAB; ATEZOLIZUMAB; HEMODIALYSIS; GEMCITABINE; PACLITAXEL; DIALYSIS; THERAPY;
D O I
10.1016/j.clgc.2019.09.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The predictive factors of hyperprogressive disease (HPD) in patients with urothelial carcinoma and renal cell carcinoma treated with programmed cell death protein 1/programmed death-ligand 1 inhibitors have not yet been characterized. We performed a retrospective study of 203 consecutive patients. We found the frequency of HPD was 6.4%, and renal impairment at the time of treatment and urothelial cell carcinoma were associated with the occurrence of HPD. Background: A rapid progression pattern called hyperprogressive disease (HPD) has been observed during early cycles of programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) inhibitor therapy. Data regarding HPD in patients with genitourinary cancer are limited. Patients and Methods: We included 203 patients with genitourinary cancer treated with PD-1/PD-L1 inhibitors between February 2015 and June 2018. HPD was defined as a greater than 50% increase in tumor burden, greater than 2-fold increase in tumor growth rate, or development of extensive (10 or more) new lesions. Results: Patients (n = 102) with renal cell carcinoma (RCC) and patients (n = 101) with urothelial carcinoma (UC) were included. HPD was observed in 13 (6.4%) patients. The median overall survival for patients with progressive disease and HPD was 7.3 months and 3.5 months, respectively. HPD occurred more frequently in patients with UC than in those with RCC (11.9% vs. 0.9%; P = .01). Multivariate analysis showed that UC and creatinine above 1.2 mg/dL were independent predictive factors for HPD. A 30% increase in lymphocyte number following PD-1/PD-L1 inhibitor treatment was a negative predictor of HPD. The incidence of HPD in patients with UC treated with paclitaxel-based chemotherapy was one-third of those treated with PD-1/PD-L1 inhibitors. Conclusion: HPD developed predominantly in patients with UC, and the incidence of HPD in patients with RCC was negligible. Treatment with PD-1/PD-L1 inhibitors should be prescribed with caution in patients with UC and creatinine above 1.2 mg/dL. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:E122 / E133
页数:12
相关论文
共 50 条
  • [1] PD-1 and PD-L1 Inhibitors as Salvage Therapy for Urothelial Carcinoma
    Sonpavde, Guru
    NEW ENGLAND JOURNAL OF MEDICINE, 2017, 376 (11): : 1073 - 1074
  • [2] Hyperprogressive disease (HPD) in genitourinary (GU) cancer patients treated with PD-1/PD-L1 inhibitors.
    Hwang, Inhwan
    Park, Inkeun
    Yoon, Shin-Kyo
    Lee, Jae-Lyun
    JOURNAL OF CLINICAL ONCOLOGY, 2019, 37 (07)
  • [3] Research progress on PD-1 and PD-L1 inhibitors in the treatment of metastatic urothelial carcinoma
    Tang, Quanqing
    Li, Shihao
    Huang, Gaozhen
    Liu, Hongwei
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2023, 119
  • [4] Targeting the PD-1/PD-L1 Pathway in Renal Cell Carcinoma
    Kammerer-Jacquet, Solene-Florence
    Deleuze, Antoine
    Saout, Judikael
    Mathieu, Romain
    Laguerre, Brigitte
    Verhoest, Gregory
    Dugay, Frederic
    Belaud-Rotureau, Marc-Antoine
    Bensalah, Karim
    Rioux-Leclercq, Nathalie
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (07)
  • [5] The future of immunotherapy in advanced renal cell carcinoma: beyond PD-1/PD-L1 inhibitors
    Nuvola, Giacomo
    Mollica, Veronica
    Massari, Francesco
    Suarez, Cristina
    IMMUNOTHERAPY, 2023, 15 (17)
  • [6] 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
    Hwang, Inhwan
    Park, Inkeun
    Yoon, Shin-Kyo
    Lee, Jae Lyun
    ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2022, 18 (04) : 371 - 377
  • [7] Evaluation of PD-1 and PD-L1 expression in canine urothelial carcinoma cell lines
    Pinard, Christopher J.
    Hocker, Samuel E.
    Poon, Andrew C.
    Inkol, Jordon M.
    Matsuyama, Arata
    Wood, R. Darren
    Wood, Geoffrey A.
    Woods, J. Paul
    Mutsaers, Anthony J.
    VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2022, 243
  • [8] Targeting PD-1/PD-L1 in the treatment of metastatic renal cell carcinoma
    Weinstock, Matthew
    McDermott, David
    THERAPEUTIC ADVANCES IN UROLOGY, 2015, 7 (06) : 365 - 377
  • [9] PD-1/PD-L1 in Renal Cell Carcinoma: Projecting the Way Forward
    Pal, Sumanta K.
    Singh, Parminder
    Vogelzang, Nicholas J.
    CLINICAL GENITOURINARY CANCER, 2015, 13 (04) : 257 - 260
  • [10] PD-1 and PD-L1 Expression in Renal Cell Carcinoma with Sarcomatoid Differentiation
    Joseph, Richard W.
    Millis, Sherri Z.
    Carballido, Estrella M.
    Bryant, David
    Gatalica, Zoran
    Reddy, Sandeep
    Bryce, Alan H.
    Vogelzang, Nicholas J.
    Stanton, Melissa L.
    Castle, Erik P.
    Ho, Thai H.
    CANCER IMMUNOLOGY RESEARCH, 2015, 3 (12) : 1303 - 1307