Updated on 2026/03/10

写真a

 
MATSUZAWA Reiko
 
Organization
Graduate School of Medicine Center for Research of Laboratory Animals and Medical Research Engineering Division for Advanced Medical Research Assistant Professor
Graduate School
Graduate School of Medicine
Undergraduate School
School of Medicine Department of Medicine
Title
Assistant Professor

Degree 1

  1. Doctor (Medicine) ( 2022.12   Nagoya University ) 

Research Areas 1

  1. Life Science / Respiratory medicine

 

Papers 5

  1. Efficacy and safety of second-line therapy of docetaxel plus ramucirumab after first-line platinum-based chemotherapy plus immune checkpoint inhibitors in non-small cell lung cancer (SCORPION): a multicenter, open-label, single-arm, phase 2 trial Reviewed

      Vol. 10 ( 66 )   2023.11

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    Authorship:Lead author   Language:English  

    DOI: 10.1016/j.eclinm.2023.102303.

  2. Favorable clinical impact of histological subtype with non-small cell carcinoma-not otherwise specified in patients with non-small cell lung cancer receiving immune checkpoint inhibitors Open Access

    Hirano, T; Tanaka, I; Morise, M; Koyama, J; Hashimoto, T; Hori, K; Matsuzawa, R; Hori, S; Karube, K; Ito, T; Sakamoto, K; Shindo, Y; Sato, M; Yokoyama, T; Kimura, T; Kondoh, Y; Ishii, M

    RESPIRATORY INVESTIGATION   Vol. 64 ( 2 ) page: 101383   2026.3

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    Language:English   Publisher:Respiratory Investigation  

    Background: Non-small cell lung cancer (NSCLC) is diagnosed using small biopsy samples obtained by bronchoscopy or transthoracic lung core biopsy, and treated with immune checkpoint inhibitors, such as programmed cell death protein-1 (PD-1) and programmed cell death protein ligand-1 (PD-L1) inhibitors, as the first-line therapy. However, the clinical benefits of first-line PD-1/PD-L1 inhibitors in non-small cell carcinoma-not otherwise specified (NSCC–NOS) remain unclear. This study aimed to clarify the clinical efficacy of first-line PD-1/PD-L1 inhibitors in patients with NSCC-NOS. Methods: We retrospectively enrolled patients with recurrent or unresectable advanced NSCLC treated with first-line PD-1/PD-L1 inhibitors, with or without chemotherapy, at three medical institutions. We adjusted for patient characteristics using propensity score matching (PSM) and analyzed the impact of the histological subtype, NSCC-NOS, on survival outcomes in patients with NSCLC treated with immunotherapy. Results: Of the 312 eligible patients, 42 (13.5%) had a histological subtype of NSCC-NOS. Significantly more patients had PD-L1 ≥ 50% in the NSCC-NOS group than in the Non NSCC-NOS group (P = 0.01). After PSM, 41 patients with NSCC-NOS and 123 with other histological subtypes (Non NSCC-NOS) were analyzed. The median progression-free survival (PFS) and the median overall survival (OS) of patients with NSCC-NOS were significantly longer than those of patients with Non NSCC-NOS, respectively (median PFS: 14.8 vs. 6.1 months, P < 0.01; median OS: 33.4 vs. 15.1 months, P = 0.04, log-rank test). Conclusions: NSCC-NOS is a histological subtype that is highly responsive to first-line PD-1/PD-L1 inhibitors with or without chemotherapy.

    DOI: 10.1016/j.resinv.2026.101383

    Open Access

    Web of Science

    Scopus

    PubMed

  3. Clinical benefit of PD-1/PD-L1 inhibitors for poor performance status patients with advanced non-small cell lung cancer

    Koyama, J; Morise, M; Tanaka, I; Hori, S; Matsuzawa, R; Ozone, S; Matsushita, A; Matsuo, M; Asano, S; Tanaka, T; Shima, K; Kimura, T; Sakamoto, K; Kondoh, Y; Hashimoto, N

    JOURNAL OF CHEMOTHERAPY     page: 1 - 10   2025.3

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    Language:English   Publisher:Journal of Chemotherapy  

    The benefit of programmed cell death protein-1 (PD-1)/programmed cell death protein ligand-1 (PD-L1) inhibitors remains unclear in non-small cell lung cancer (NSCLC) patients with poor performance status (PS). In the current multi-centre retrospective cohort study, advanced or recurrent NSCLC patients treated with PD-1/PD-L1 inhibitors were enrolled. Of the 219 patients enrolled, 44 had PS 2–4. The objective response rate (ORR) of patients with PS 2–4 in 1<sup>st</sup> line was 33%. Among 1<sup>st</sup> line group, median progression-free survival (PFS) in patients with PS 2 was significantly longer compared to that in patients with PS 3–4 (15.3 months vs. 0.9 months, P = 0.039, Log-rank test). Among previously treated patients, the ORR of patients with PS 2–4 was only 4%, and PFS and overall survival was poor even in patients with PS 2. PD-1/PD-L1 inhibitors can be an option for PS 2 NSCLC patients in 1<sup>st</sup> line setting.

    DOI: 10.1080/1120009X.2025.2481349

    Web of Science

    Scopus

    PubMed

  4. Non-invasive early prediction of immune checkpoint inhibitor efficacy in non-small-cell lung cancer patients using on-treatment serum CRP and NLR Invited Reviewed Open Access

    J Cancer Res Clin Oncol   Vol. 149 ( 7 ) page: 3885 - 3893   2023.8

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    Authorship:Lead author  

    DOI: 10.1007/s00432-022-04300-x

  5. Factors influencing the concordance of histological subtype diagnosis from biopsy and resected specimens of lung adenocarcinoma Reviewed

    Lung Cancer   Vol. 94   page: 1 - 6   2016.4

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    Authorship:Lead author   Language:English