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      Hypofractionated carbon‐ion radiotherapy for stage I peripheral nonsmall cell lung cancer (GUNMA0701): Prospective phase II study

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          Abstract

          This phase II study's aim was to confirm the efficacy and safety of hypofractionated carbon‐ion radiotherapy in patients with stage I peripheral nonsmall cell lung cancer (NSCLC). The study encompassed 37 patients with histologically proven peripheral stage I NSCLC in the period June 2010‐March 2015. All underwent the planned full dose of carbon‐ion radiotherapy, administered with relative biological effectiveness of 52.8 Gy and 60 Gy (divided into four fractions over 1 week) for T1 and T2a tumors, respectively. The 2‐year local control rate was set as the primary endpoint, while overall survival, progression‐free survival, and the incidence rates of acute and late adverse events were secondary endpoints. The patients were followed up for 56.3 months overall and 62.2 months in the surviving patients, respectively. The actuarial local control rates were 91.2% after 2 years, and 88.1% after 5 years. No differences were found between the T1 and T2a tumors in the 5‐year local control rate (90.9% vs 86.7%, P = .75). The actuarial overall survival rates achieved 91.9% for 2‐year and 74.9% for 5‐year period. T1 tumors showed actuarial 5‐year overall survival rates of 80%, compared to 66.7% in T2a tumors. Two patients with T2a tumors and either severe emphysema or bronchiectasis experienced lung toxicity ≥ grade 2, in contrast to T1 patients who only experienced mild toxicities (lower than grade 2). The findings suggest that carbon‐ion radiotherapy is effective and safe for peripheral stage I NSCLC; however, further clinical evaluations are needed to confirm its therapeutic efficacy.

          Trial registration: UMIN000003797. Registered 21 June 2010, prospectively registered.

          Abstract

          The aim of this phase II study was to confirm the feasibility and safety of hypofractionated carbon‐ion radiotherapy for patients with stage I peripheral nonsmall cell lung cancer. The actuarial 2‐year and 5‐year local control rates were 91.2% and 88.1%, respectively. The actuarial 2‐year and 5‐year overall survival rates were 91.9% and 74.9%, respectively.

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          Randomized trial of lobectomy versus limited resection for T1 N0 non-small cell lung cancer. Lung Cancer Study Group.

          It has been reported that limited resection (segment or wedge) is equivalent to lobectomy in the management of early stage (T1-2 N0) non-small cell lung cancer. A prospective, multiinstitutional randomized trial was instituted comparing limited resection with lobectomy for patients with peripheral T1 N0 non-small cell lung cancer documented at operation. Analysis included locoregional and distant recurrence rates, 5-year survival rates, perioperative morbidity and mortality, and late pulmonary function assessment. There were 276 patients randomized, with 247 patients eligible for analysis. There were no significant differences for all stratification variables, selected prognostic factors, perioperative morbidity, mortality, or late pulmonary function. In patients undergoing limited resection, there was an observed 75% increase in recurrence rates (p = 0.02, one-sided) attributable to an observed tripling of the local recurrence rate (p = 0.008 two-sided), an observed 30% increase in overall death rate (p = 0.08, one-sided), and an observed 50% increase in death with cancer rate (p = 0.09, one-sided) compared to patients undergoing lobectomy (p = 0.10, one-sided was the predefined threshold for statistical significance for this equivalency study). Compared with lobectomy, limited pulmonary resection does not confer improved perioperative morbidity, mortality, or late postoperative pulmonary function. Because of the higher death rate and locoregional recurrence rate associated with limited resection, lobectomy still must be considered the surgical procedure of choice for patients with peripheral T1 N0 non-small cell lung cancer.
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            Outcome in a prospective phase II trial of medically inoperable stage I non-small-cell lung cancer patients treated with stereotactic body radiotherapy.

            The impact of stereotactic body radiotherapy (SBRT) on 3-year progression-free survival of medically inoperable patients with stage I non-small-cell lung cancer (NSCLC) was analyzed in a prospective phase II study. Fifty-seven patients with T1NOMO (70%) and T2N0M0 (30%) were included between August 2003 and September 2005 at seven different centers in Sweden, Norway, and Denmark and observed up to 36 months. SBRT was delivered with 15 Gy times three at the 67% isodose of the planning target volume. Progression-free survival at 3 years was 52%. Overall- and cancer-specific survival at 1, 2, and 3 years was 86%, 65%, 60%, and 93%, 88%, 88%, respectively. There was no statistically significant difference in survival between patients with T1 or T2 tumors. At a median follow-up of 35 months (range, 4 to 47 months), 27 patients (47%) were deceased, seven as a result of lung cancer and 20 as a result of concurrent disease. Kaplan-Meier estimated local control at 3 years was 92%. Local relapse was observed in four patients (7%). Regional relapse was observed in three patients (5%). Nine patients (16%) developed distant metastases. The estimated risk of all failure (local, regional, or distant metastases) was increased in patients with T2 (41%) compared with those with T1 (18%) tumors (P = .027). With a 3-year local tumor control rate higher than 90% with limited toxicity, SBRT emerges as state-of-the-art treatment for medically inoperable stage I NSCLC and may even challenge surgery in operable instances.
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              Stereotactic body radiation therapy for early-stage non-small-cell lung carcinoma: four-year results of a prospective phase II study.

              The 50-month results of a prospective Phase II trial of stereotactic body radiation therapy (SBRT) in medically inoperable patients are reported. A total of 70 medically inoperable patients had clinically staged T1 (34 patients) or T2 (36 patients) ( 20 cc) did not significantly impact survival: MS was 36.9 months (95% CI, 18.1-42.9), 34.0 (95% CI, 16.9-57.1), 32.8 (95% CI, 21.3-57.8), and 21.4 months (95% CI, 17.8-41.6), respectively (p = 0.712). There was no significant survival difference between patients with peripheral vs. central tumors (MS 33.2 vs. 24.4 months, p = 0.697). Grade 3 to 5 toxicity occurred in 5 of 48 patients with peripheral lung tumors (10.4%) and in 6 of 22 patients (27.3%) with central tumors (Fisher's exact test, p = 0.088). Based on our study results, use of SBRT results in high rates of local control in medically inoperable patients with Stage I NSCLC.
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                Author and article information

                Contributors
                junsaito@med.u-toyama.ac.jp
                Journal
                Cancer Med
                Cancer Med
                10.1002/(ISSN)2045-7634
                CAM4
                Cancer Medicine
                John Wiley and Sons Inc. (Hoboken )
                2045-7634
                18 September 2019
                November 2019
                : 8
                : 15 ( doiID: 10.1002/cam4.v8.15 )
                : 6644-6650
                Affiliations
                [ 1 ] Gunma University Heavy Ion Medical Center Maebashi Gunma Japan
                [ 2 ] Department of Radiation Oncology Faculty of Medicine University of Toyama Toyama Toyama Japan
                [ 3 ] Department of Radiology Saitama Medical Center Jichi Medical University Saitama Japan
                [ 4 ] Department of Radiation Oncology Gunma Prefectural Cancer Center Ota Gunma Japan
                [ 5 ] Department of Radiation Oncology School of Medicine Kyorin University Mitaka Tokyo Japan
                [ 6 ] Department of Respiratory Medicine Gunma Prefectural Cancer Center Ota Gunma Japan
                [ 7 ] Department of Respiratory Medicine National Hospital Organization Shibukawa Medical Center Shibukawa Gunma Japan
                [ 8 ] Department of Medicine and Molecular Science Gunma University Graduate School of Medicine Maebashi Gunma Japan
                Author notes
                [*] [* ] Correspondence

                Jun‐ichi Saitoh, Department of Radiation Oncology, Faculty of Medicine, University of Toyama, 2630 Sugitani, Toyama, Toyama 930‐0194, Japan.

                Email: junsaito@ 123456med.u-toyama.ac.jp

                Author information
                https://orcid.org/0000-0001-7863-6023
                https://orcid.org/0000-0001-6209-9446
                Article
                CAM42561
                10.1002/cam4.2561
                6825999
                31532584
                7bbb4f6f-b702-4867-b767-ded906b45b99
                © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 July 2019
                : 04 September 2019
                : 04 September 2019
                Page count
                Figures: 3, Tables: 3, Pages: 7, Words: 5081
                Funding
                Funded by: Gunma University Heavy Ion Medical Center
                Categories
                Original Research
                Clinical Cancer Research
                Original Research
                Custom metadata
                2.0
                November 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.0 mode:remove_FC converted:03.11.2019

                Oncology & Radiotherapy
                carbon‐ion radiotherapy,heavy ion radiotherapy,nonsmall cell lung cancer,phase ii clinical trial,prospective study

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