Pseudoprogression in Previously Treated Patients with Non-Small Cell Lung Cancer Who Received Nivolumab Monotherapy.


Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
03 2019
Historique:
received: 19 08 2018
revised: 24 10 2018
accepted: 27 10 2018
pubmed: 24 11 2018
medline: 17 4 2020
entrez: 24 11 2018
Statut: ppublish

Résumé

Nivolumab is effective in the treatment of previously treated patients with advanced NSCLC. However, its radiological evaluation is challenging because of atypical patterns of response such as pseudoprogression. We examined the characteristics and outcomes of previously treated patients with NSCLC who were treated with nivolumab and experienced development of pseudoprogression. We conducted a 15-center retrospective cohort study of previously treated patients with advanced NSCLC who received nivolumab monotherapy. For the patients who showed pseudoprogression, we defined progression-free survival 1 (PFS1) as the time to Response Evaluation Criteria in Solid Tumors-defined first progressive disease and progression-free survival 2 (PFS2) as the time to Response Evaluation Criteria in Solid Tumors-defined second progressive disease or death. Among the 542 patients included, 20% and 53% showed a typical response and progression, respectively. Of the 14 (3%) patients who showed pseudoprogression, most (n = 10) showed a response within 3 months of nivolumab treatment. The median PFS1 and PFS2 were 1.0 and 7.3 months, respectively. The median PFS2 was significantly shorter in the patients who showed pseudoprogression than the PFS of the patients with a typical response (p < 0.001). In contrast, patients showing pseudoprogression had significantly longer overall survival than did patients showing typical progression (p = 0.001). Pseudoprogression was uncommon, and the duration of response in patients who showed pseudoprogression was shorter than that in patients who showed a typical response. However, the survival benefit of pseudoprogression was markedly better than that of typical progression. Further research is required to elucidate the characteristics of and mechanisms underlying pseudoprogression.

Identifiants

pubmed: 30468872
pii: S1556-0864(18)33418-X
doi: 10.1016/j.jtho.2018.10.167
pii:
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Nivolumab 31YO63LBSN

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

468-474

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2018 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

Auteurs

Daichi Fujimoto (D)

Department of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Japan. Electronic address: daichi@kcho.jp.

Hiroshige Yoshioka (H)

Department of Respiratory Medicine, Kurashiki Central Hospital, Kurashiki, Japan.

Yuki Kataoka (Y)

Department of Respiratory Medicine, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Japan.

Takeshi Morimoto (T)

Clinical Research Center, Kobe City Medical Center General Hospital, Kobe, Japan; Department of Clinical Epidemiology, Hyogo College of Medicine, Nishinomiya, Japan.

Tae Hata (T)

Department of Respiratory Medicine, Kurashiki Central Hospital, Kurashiki, Japan.

Young Hak Kim (YH)

Department of Respiratory Medicine, Kyoto University Hospital, Kyoto, Japan.

Keisuke Tomii (K)

Department of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Japan.

Tadashi Ishida (T)

Department of Respiratory Medicine, Kurashiki Central Hospital, Kurashiki, Japan.

Masataka Hirabayashi (M)

Department of Respiratory Medicine, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Japan.

Satoshi Hara (S)

Department of Respiratory Medicine, Itami City Hospital, Itami, Japan.

Manabu Ishitoko (M)

Department of Respiratory Medicine, Shiga General Hospital, Moriyama, Japan.

Yasushi Fukuda (Y)

Department of Respiratory Medicine, Himeji Medical Center, Himeji, Japan.

Moon Hee Hwang (MH)

Department of Respiratory Medicine, Osaka Red Cross Hospital, Osaka, Japan.

Naoki Sakai (N)

Department of Respiratory Medicine, Otsu Red Cross Hospital, Otsu, Japan.

Motonari Fukui (M)

Respiratory Disease Center, Kitano Hospital, The Tazuke-Kofukai Medical Research Institute, Osaka, Japan.

Hitoshi Nakaji (H)

Department of Respiratory Medicine, Toyooka Public Hospital, Toyooka, Japan.

Mitsunori Morita (M)

Department of Respiratory Medicine, Kobe City Medical Center West Hospital, Kobe, Japan.

Tadashi Mio (T)

Division of Respiratory Medicine, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.

Takehiro Yasuda (T)

Department of Respiratory Medicine, Tenri Hospital, Nara, Japan.

Takakazu Sugita (T)

Department of Respiratory Medicine, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.

Toyohiro Hirai (T)

Department of Respiratory Medicine, Kyoto University Hospital, Kyoto, Japan.

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Classifications MeSH