Pembrolizumab monotherapy in patients with previously treated metastatic high-grade neuroendocrine neoplasms: joint analysis of two prospective, non-randomised trials

被引:94
作者
Vijayvergia, Namrata [1 ]
Dasari, Arvind [2 ]
Deng, Mengying [1 ]
Litwin, Samuel [1 ]
Al-Toubah, Taymeyah [3 ]
Alpaugh, R. Katherine [1 ]
Dotan, Efrat [1 ]
Hall, Michael J. [1 ]
Ross, Nicole M. [1 ]
Runyen, Melissa M. [1 ]
Denlinger, Crystal S. [1 ]
Halperin, Daniel M. [2 ]
Cohen, Steven J. [4 ]
Engstrom, Paul F. [1 ]
Strosberg, Jonathan R. [3 ]
机构
[1] Fox Chase Canc Ctr, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[2] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[4] Jefferson Hlth, Abington Hosp, Abington, PA USA
关键词
SMALL-CELL; PROGNOSTIC-FACTORS; TUMORS; CARCINOMAS; CLASSIFICATION; ETOPOSIDE; LUNG; G3; CHEMOTHERAPY; NIVOLUMAB;
D O I
10.1038/s41416-020-0775-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Metastatic high-grade neuroendocrine neoplasms (G3NENs) have limited treatment options after progression on platinum-based therapy. We addressed the role of Pembrolizumab in patients with previously treated metastatic G3NENs. Methods Two open-label, phase 2 studies enrolled patients with G3NEN (Ki-67 > 20%) to receive Pembrolizumab at 200 mg I.V. every 3 weeks. Radiographic evaluation was conducted every 9 weeks with overall response rate as the primary endpoint. Results Between November 2016 and May 2018, 29 patients (13 males/16 females) with G3NENs were enrolled. One patient (3.4%) had an objective response and an additional six patients (20.7%) had stable disease, resulting in a disease control rate of 24.1%. Disease control rate (DCR) at 18 weeks was 10.3% (3/29). There was no difference in the DCR, PFS or OS between the PD-L1-negative and -positive groups (p 0.56, 0.88 and 0.55, respectively). Pembrolizumab was well tolerated with only 9 grade 3, and no grade 4 events considered drug-related. Conclusions Pembrolizumab can be safely administered to patients with G3NENs but has limited activity as a single agent. Successful completion of our trials suggest studies in G3NENs are feasible and present an unmet need. Further research to identify active combination therapies should be considered.
引用
收藏
页码:1309 / 1314
页数:6
相关论文
共 44 条
  • [1] Genomic profiling to distinguish poorly differentiated neuroendocrine carcinomas arising in different sites
    Bergsland, Emily K.
    Roy, Ritu
    Stephens, Phil
    Ross, Jeffrey S.
    Bailey, Mark
    Olshen, Adam
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (15)
  • [2] Nivolumab versus Docetaxel in Advanced Squamous-Cell Non-Small-Cell Lung Cancer
    Brahmer, Julie
    Reckamp, Karen L.
    Baas, Paul
    Crino, Lucio
    Eberhardt, Wilfried E. E.
    Poddubskaya, Elena
    Antonia, Scott
    Pluzanski, Adam
    Vokes, Everett E.
    Holgado, Esther
    Waterhouse, David
    Ready, Neal
    Gainor, Justin
    Aren Frontera, Osvaldo
    Havel, Libor
    Steins, Martin
    Garassino, Marina C.
    Aerts, Joachim G.
    Domine, Manuel
    Paz-Ares, Luis
    Reck, Martin
    Baudelet, Christine
    Harbison, Christopher T.
    Lestini, Brian
    Spigel, David R.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (02) : 123 - 135
  • [3] Chung H. C., 2018, PHASE 2 STUDY PEMBRO
  • [4] Comparative Study of Lung and Extrapulmonary Poorly Differentiated Neuroendocrine Carcinomas: A SEER Database Analysis of 162,983 Cases
    Dasari, Arvind
    Mehta, Kathan
    Byers, Lauren A.
    Sorbye, Halfdan
    Yao, James C.
    [J]. CANCER, 2018, 124 (04) : 807 - 815
  • [5] Heterogeneity of grade 3 gastroenteropancreatic neuroendocrine carcinomas: New insights and treatment implications
    Fazio, Nicola
    Milione, Massimo
    [J]. CANCER TREATMENT REVIEWS, 2016, 50 : 61 - 67
  • [6] PD-L1 Expression and Immune Cell In fi ltration in Gastroenteropancreatic (GEP) and Non-GEP Neuroendocrine Neoplasms With High Proliferative Activity
    Ferrata, Martina
    Schad, Arno
    Zimmer, Stefanie
    Musholt, Thomas J.
    Bahr, Katharina
    Kuenzel, Julian
    Becker, Sven
    Springer, Erik
    Roth, Wilfried
    Weber, Matthias M.
    Fottner, Christian
    [J]. FRONTIERS IN ONCOLOGY, 2019, 9
  • [7] Galanis E, 1997, CANCER-AM CANCER SOC, V79, P1729, DOI 10.1002/(SICI)1097-0142(19970501)79:9<1729::AID-CNCR14>3.0.CO
  • [8] 2-#
  • [9] Safety and Tumor Responses with Lambrolizumab (Anti-PD-1) in Melanoma
    Hamid, Omid
    Robert, Caroline
    Daud, Adil
    Hodi, F. Stephen
    Hwu, Wen-Jen
    Kefford, Richard
    Wolchok, Jedd D.
    Hersey, Peter
    Joseph, Richard W.
    Weber, Jeffrey S.
    Dronca, Roxana
    Gangadhar, Tara C.
    Patnaik, Amita
    Zarour, Hassane
    Joshua, Anthony M.
    Gergich, Kevin
    Elassaiss-Schaap, Jeroen
    Algazi, Alain
    Mateus, Christine
    Boasberg, Peter
    Tumeh, Paul C.
    Chmielowski, Bartosz
    Ebbinghaus, Scot W.
    Li, Xiaoyun Nicole
    Kang, S. Peter
    Ribas, Antoni
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2013, 369 (02) : 134 - 144
  • [10] Characteristics and treatment of patients with G3 gastroenteropancreatic neuroendocrine neoplasms
    Heetfeld, M.
    Chougnet, C. N.
    Olsen, I. H.
    Rinke, A.
    Borbath, I.
    Crespo, G.
    Barriuso, J.
    Pavel, M.
    O'Toole, D.
    Walter, T.
    [J]. ENDOCRINE-RELATED CANCER, 2015, 22 (04) : 657 - 664