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      A single arm Phase I/II trial on the combination of carboplatin, nab-paclitaxel and avastin as first-line treatment for advanced non-squamous non-small cell lung cancer (TORG1424/OLCSG1402: CARNAVAL)

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          Abstract

          Background

          Bevacizumab with platinum doublet therapy including paclitaxel + carboplatin improves the survival of patients with non-squamous non-small cell lung cancer. However, in a previous trial (CA031), paclitaxel + carboplatin led to Grade > 3 neutropenia in a Japanese population. Nanoparticle albumin-bound paclitaxel exhibits an improved toxicity profile. We evaluated the safety, dosage and response rate of the nanoparticle albumin-bound paclitaxel + carboplatin + bevacizumab combination in a Japanese population.

          Methods

          Chemotherapy-naive patients with advanced non-squamous non-small cell lung cancer were included. The dosage schedule was established in the Phase I trial as follows: 4–6 cycles of carboplatin (area under the concentration–time curve = 6 on Day 1) + nanoparticle albumin-bound paclitaxel (100 mg/m 2 on Days 1, 8 and 15) + bevacizumab (15 mg/kg on Day 1), followed by maintenance therapy (nanoparticle albumin-bound paclitaxel + bevacizumab). The response rate and presence of adverse effects were evaluated in the Phase II trial.

          Results

          The overall response rate was 56.5% (90% confidence interval: 44.5–68.5), and 93% of patients (43/46) showed tumor shrinkage or maintained a stable disease course. The primary endpoint was achieved. At the median follow-up duration of 42 months, the median overall survival was 18.9 (range: 10.5–32.4) months. The most frequently observed Grade ≥ 3 adverse effects were neutropenia (72%), leukopenia (50%) and anemia (30%).

          Conclusions

          All adverse effects were manageable and none resulted in patient death. In conclusion, the nanoparticle albumin-bound paclitaxel + carboplatin + bevacizumab combination is favorable and well tolerated in Japanese patients as first-line treatment for advanced non-squamous non-small cell lung cancer.

          Abstract

          The combination of the nanoparticle albumin-bound paclitaxel + carboplatin + bevacizumab as first-line treatment for advanced non-squamous non-small cell lung cancer is revealed to be favorable and well tolerated in Japanese patients.

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          Most cited references33

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          Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.

          Estimates of the worldwide incidence and mortality from 27 major cancers and for all cancers combined for 2012 are now available in the GLOBOCAN series of the International Agency for Research on Cancer. We review the sources and methods used in compiling the national cancer incidence and mortality estimates, and briefly describe the key results by cancer site and in 20 large "areas" of the world. Overall, there were 14.1 million new cases and 8.2 million deaths in 2012. The most commonly diagnosed cancers were lung (1.82 million), breast (1.67 million), and colorectal (1.36 million); the most common causes of cancer death were lung cancer (1.6 million deaths), liver cancer (745,000 deaths), and stomach cancer (723,000 deaths). © 2014 UICC.
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            Pembrolizumab versus Chemotherapy for PD-L1–Positive Non–Small-Cell Lung Cancer

            Pembrolizumab is a humanized monoclonal antibody against programmed death 1 (PD-1) that has antitumor activity in advanced non-small-cell lung cancer (NSCLC), with increased activity in tumors that express programmed death ligand 1 (PD-L1).
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              Pembrolizumab plus Chemotherapy in Metastatic Non–Small-Cell Lung Cancer

              First-line therapy for advanced non-small-cell lung cancer (NSCLC) that lacks targetable mutations is platinum-based chemotherapy. Among patients with a tumor proportion score for programmed death ligand 1 (PD-L1) of 50% or greater, pembrolizumab has replaced cytotoxic chemotherapy as the first-line treatment of choice. The addition of pembrolizumab to chemotherapy resulted in significantly higher rates of response and longer progression-free survival than chemotherapy alone in a phase 2 trial.
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                Author and article information

                Contributors
                Journal
                Jpn J Clin Oncol
                Jpn J Clin Oncol
                jjco
                Japanese Journal of Clinical Oncology
                Oxford University Press
                0368-2811
                1465-3621
                July 2024
                09 April 2024
                09 April 2024
                : 54
                : 7
                : 805-812
                Affiliations
                Department of Community Medicine , Pulmonology and Cardiology, Ehime University Graduate School of Medicine , Toon, Japan
                Center for Clinical Oncology, Okayama University Hospital , Okayama, Japan
                Department of Respiratory Medicine, Japanese Red Cross Okayama Hospital , Okayama, Japan
                Department of Respiratory Medicine, Japanese Red Cross Okayama Hospital , Okayama, Japan
                Department of Respiratory Medicine, Kurashiki Central Hospital , Kurashiki, Japan
                Department of Respiratory Medicine, Kurashiki Central Hospital , Kurashiki, Japan
                Division of Medical Oncology , Department of Internal Medicine, Teikyo University School of Medicine , Tokyo, Japan
                Division of Medical Oncology , Department of Internal Medicine, Teikyo University School of Medicine , Tokyo, Japan
                Department of Respiratory Medicine, Okayama Rosai Hospital , Okayama, Japan
                Department of Thoracic Oncology, Kanagawa Cancer Center , Yokohama, Japan
                Department of Allergy and Respiratory Medicine, Gunma University Graduate School of Medicine , Maebashi, Japan
                Department of Respiratory Medicine, Japan Community Health Care Organization Hokkaido Hospital , Sapporo, Japan
                Department of Respiratory Medicine, Japanese Red Cross Himeji Hospital , Himeji, Japan
                Department of Medical Oncology, Graduate School of Medicine, Chiba University , Chiba, Japan
                Department of Respirology Medicine and Medical Oncology, Yokohama Municipal Citizen’s Hospital , Yokohama, Japan
                Department of Allergy and Respiratory Medicine, Okayama University Hospital , Okayama, Japan
                Clinical Research Center, National Hospital Organization Shikoku Cancer Center , Matsuyama, Japan
                Department of Respirology Medicine and Medical Oncology, Yokohama Municipal Citizen’s Hospital , Yokohama, Japan
                Author notes
                For reprints and all correspondence: Toshio Kubo, Center for Clinical Oncology, Okayama University Hospital, 2-5-1 Shikata-Cho, Kita-Ku, Okayama 700-8558, Japan. E-mail: t-kubo@ 123456cc.okayama-u.ac.jp

                Present address: Department of Respiratory Medicine, Comprehensive Cancer Center, International Medical Center, Saitama Medical University, 1397-1 Yamane, Hidaka 350-1298, Japan

                Author information
                https://orcid.org/0000-0002-2545-3052
                https://orcid.org/0000-0001-5104-5493
                https://orcid.org/0000-0001-5548-7686
                https://orcid.org/0000-0002-9172-9379
                Article
                hyae044
                10.1093/jjco/hyae044
                11228859
                38594880
                1223ba72-8073-4965-a125-0014d9d4907a
                © The Author(s) 2024. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 09 January 2024
                : 18 March 2024
                : 20 March 2024
                Page count
                Pages: 8
                Funding
                Funded by: Taiho Pharmaceutical Co, Ltd;
                Categories
                Original Article
                AcademicSubjects/MED00300

                Oncology & Radiotherapy
                nsclc,japanese population,neutropenia,dosing scheme,bevacizumab
                Oncology & Radiotherapy
                nsclc, japanese population, neutropenia, dosing scheme, bevacizumab

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