Association Between Skin Reaction and Clinical Benefit in Patients Treated with Anti-Programmed Cell Death 1 Monotherapy for Advanced Non-Small Cell Lung Cancer
Anti-programmed cell death 1 antibody is a standard therapy for advanced non-small cell lung cancer (NSCLC). However, immune-related adverse events (irAEs), such as skin reactions, are frequently observed. Although skin reactions are associated with clinical efficacy in melanoma, this association in...
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Published in | The oncologist (Dayton, Ohio) Vol. 25; no. 3; pp. e536 - e544 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
John Wiley & Sons, Inc
01.03.2020
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Abstract | Anti-programmed cell death 1 antibody is a standard therapy for advanced non-small cell lung cancer (NSCLC). However, immune-related adverse events (irAEs), such as skin reactions, are frequently observed. Although skin reactions are associated with clinical efficacy in melanoma, this association in advanced NSCLC and predictors of irAEs remain unclear. Accordingly, this study identified potential correlations of skin reactions with clinical efficacy and clinical predictors of development of skin reactions.
We retrospectively surveyed patients with advanced NSCLC who received nivolumab or pembrolizumab monotherapy at Sendai Kousei Hospital (n = 155) during January 2016 to April 2018. Treatment efficacy was evaluated in patients with and without skin reactions, and associated predictive markers were determined. A 6-week landmark analysis was conducted to assess the clinical benefit of early skin reactions.
Skin reactions were observed in 51 patients with a median time to onset of 6.4 weeks. The overall response rate (ORR) was significantly higher in patients with skin reactions (57% vs. 19%, p < .001). Median progression-free survival (PFS) durations of 12.9 and 3.5 months and overall survival durations of not reached and 11.4 months were observed in patients with and without skin reactions, respectively. In the 6-week landmark analysis, the ORR was significantly higher in patients with skin reactions, and skin reactions were significantly associated with increased PFS. A multivariate analysis identified pre-existing rheumatoid factor (RF) as an independent predictor of skin reactions.
Skin reactions appeared beneficial in patients treated with nivolumab/pembrolizumab for advanced NSCLC and could be predicted by pre-existing RF. Further large-scale validations studies are warranted.
This single-institutional medical record review that included 155 patients with advanced non-small cell lung cancer who were treated with nivolumab or pembrolizumab monotherapy revealed that overall response rate and progression-free survival were significantly better in patients with skin reactions. Pre-existing rheumatoid factor was an independent predictor of skin reactions. |
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AbstractList | Skin reactions are common immune‐related adverse events associated with PD‐1 therapy. This study investigated the association between the development of skin reactions and clinical benefit of skin reaction, as well as associated predictive markers, in patients with advanced non‐small cell lung cancer who were treated with nivolumab or pembrolizumab monotherapy. Anti-programmed cell death 1 antibody is a standard therapy for advanced non-small cell lung cancer (NSCLC). However, immune-related adverse events (irAEs), such as skin reactions, are frequently observed. Although skin reactions are associated with clinical efficacy in melanoma, this association in advanced NSCLC and predictors of irAEs remain unclear. Accordingly, this study identified potential correlations of skin reactions with clinical efficacy and clinical predictors of development of skin reactions. We retrospectively surveyed patients with advanced NSCLC who received nivolumab or pembrolizumab monotherapy at Sendai Kousei Hospital (n = 155) during January 2016 to April 2018. Treatment efficacy was evaluated in patients with and without skin reactions, and associated predictive markers were determined. A 6-week landmark analysis was conducted to assess the clinical benefit of early skin reactions. Skin reactions were observed in 51 patients with a median time to onset of 6.4 weeks. The overall response rate (ORR) was significantly higher in patients with skin reactions (57% vs. 19%, p < .001). Median progression-free survival (PFS) durations of 12.9 and 3.5 months and overall survival durations of not reached and 11.4 months were observed in patients with and without skin reactions, respectively. In the 6-week landmark analysis, the ORR was significantly higher in patients with skin reactions, and skin reactions were significantly associated with increased PFS. A multivariate analysis identified pre-existing rheumatoid factor (RF) as an independent predictor of skin reactions. Skin reactions appeared beneficial in patients treated with nivolumab/pembrolizumab for advanced NSCLC and could be predicted by pre-existing RF. Further large-scale validations studies are warranted. This single-institutional medical record review that included 155 patients with advanced non-small cell lung cancer who were treated with nivolumab or pembrolizumab monotherapy revealed that overall response rate and progression-free survival were significantly better in patients with skin reactions. Pre-existing rheumatoid factor was an independent predictor of skin reactions. |
Author | Ono, Kana Domeki, Yutaka Toi, Yukihiro Kawana, Sachiko Aso, Mari Kawashima, Yosuke Nakamura, Atsushi Yamanda, Shinsuke Kimura, Yuichiro Sugawara, Shunichi Shimizu, Hisashi Tsurumi, Kyoji Terayama, Keisuke Sugisaka, Jun Aiba, Tomoiki Ogasawara, Takahiro Saito, Ryohei Honda, Yoshihiro |
AuthorAffiliation | 1 Department of Pulmonary Medicine, Sendai Kousei Hospital Aoba‐ku, Sendai Miyagi Japan |
AuthorAffiliation_xml | – name: 1 Department of Pulmonary Medicine, Sendai Kousei Hospital Aoba‐ku, Sendai Miyagi Japan |
Author_xml | – sequence: 1 givenname: Mari surname: Aso fullname: Aso, Mari organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 2 givenname: Yukihiro surname: Toi fullname: Toi, Yukihiro organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 3 givenname: Jun surname: Sugisaka fullname: Sugisaka, Jun organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 4 givenname: Tomoiki surname: Aiba fullname: Aiba, Tomoiki organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 5 givenname: Sachiko surname: Kawana fullname: Kawana, Sachiko organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 6 givenname: Ryohei surname: Saito fullname: Saito, Ryohei organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 7 givenname: Takahiro surname: Ogasawara fullname: Ogasawara, Takahiro organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 8 givenname: Kyoji surname: Tsurumi fullname: Tsurumi, Kyoji organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 9 givenname: Kana surname: Ono fullname: Ono, Kana organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 10 givenname: Hisashi surname: Shimizu fullname: Shimizu, Hisashi organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 11 givenname: Yutaka surname: Domeki fullname: Domeki, Yutaka organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 12 givenname: Keisuke surname: Terayama fullname: Terayama, Keisuke organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 13 givenname: Yosuke surname: Kawashima fullname: Kawashima, Yosuke organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 14 givenname: Atsushi surname: Nakamura fullname: Nakamura, Atsushi organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 15 givenname: Shinsuke surname: Yamanda fullname: Yamanda, Shinsuke organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 16 givenname: Yuichiro surname: Kimura fullname: Kimura, Yuichiro organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 17 givenname: Yoshihiro surname: Honda fullname: Honda, Yoshihiro organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan – sequence: 18 givenname: Shunichi surname: Sugawara fullname: Sugawara, Shunichi organization: Department of Pulmonary Medicine, Sendai Kousei Hospital, Aoba-ku, Sendai, Miyagi, Japan |
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Keywords | Rheumatoid factor Immune-related adverse events Skin reaction Immunotherapy Lung cancer Programmed cell death 1 |
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Notes | Disclosures of potential conflicts of interest may be found at the end of this article. |
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Title | Association Between Skin Reaction and Clinical Benefit in Patients Treated with Anti-Programmed Cell Death 1 Monotherapy for Advanced Non-Small Cell Lung Cancer |
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