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A modified Phase I trial of radiation dose escalation in 3D conformal radiation therapy with concurrent vinorelbine and carboplatin chemotherapy for non-small-cell lung cancer

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机构: [1]Hebei Med Univ, Dept Oncol, N China Petr Bur Gen Hosp, Renqiu City, Hebei 062552, Peoples R China [2]Hebei Univ Hosp, Dept Radiat Oncol, Baoding 071000, Hebei, Peoples R China [3]Okayama Univ, Dept Oral & Maxillofacial Radiol, Field Tumor Biol, Grad Sch Med Dent & Pharmaceut Sci, Okayama 7008525, Japan
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关键词: non-small-cell lung cancer 3D conformal radiation therapy dose escalation concurrent chemoradiotherapy

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The Radiation Therapy Oncology Group reported a maximum tolerated dose of 74 Gy for patients with non-small cell lung cancer (NSCLC); however, it was unclear whether this dose could be safely administered to Asian patients due to differences in their physique compared to Western patients. We therefore conducted a modified Phase I trial to determine whether 70 Gy could be safely delivered to Chinese patients with NSCLC undergoing 3D-conformal radiation therapy (3D-CRT) with concurrent chemotherapy. Previously untreated NSCLC patients received 3D-CRT (2 Gy/day, 5 fractions per week). Three dose levels were examined: 62, 66 and 70 Gy. Two cycles of concurrent chemotherapy (vinorelbine and carboplatin) were started on the first day of radiation therapy. Dose-limiting toxicity (DLT) was defined as severe or life-threatening side effects that altered the continued implementation of chemoradiotherapy. Among the 19 patients recruited in this study, most of the haematologic and non-haematologic toxicities were mild to moderate and clinically manageable. Only one patient, in the 70 Gy cohort, experienced a DLT of Grade 3 radiation-induced pneumonia. The overall response rate was 77.8% (14/18). The median progression-free survival (PFS) was 12 months, and the 1-year PFS was 37.6%. Our results support both the feasibility of incorporating 3D-CRT with concurrent vinorelbine and carboplatin and a dose escalation to 70 Gy for Chinese patients with NSCLC, based on the acceptable toxicity and encouraging overall response and survival rates. A further evaluation of this regimen in a prospective Phase II trial is ongoing.

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出版当年[2014]版:
大类 | 4 区 医学
小类 | 4 区 生物学 4 区 核医学
最新[2025]版:
大类 | 4 区 医学
小类 | 3 区 生物学 4 区 肿瘤学 4 区 核医学
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出版当年[2013]版:
Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Q2 BIOLOGY
最新[2023]版:
Q2 BIOLOGY Q3 ONCOLOGY Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING

影响因子: 最新[2023版] 最新五年平均 出版当年[2013版] 出版当年五年平均 出版前一年[2012版] 出版后一年[2014版]

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第一作者机构: [1]Hebei Med Univ, Dept Oncol, N China Petr Bur Gen Hosp, Renqiu City, Hebei 062552, Peoples R China [*1]Hebei Med Univ, Dept Oncol, N China Petr Bur Gen Hosp, 8 Huizhan Ave, Renqiu City, Hebei 062552, Peoples R China
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通讯机构: [1]Hebei Med Univ, Dept Oncol, N China Petr Bur Gen Hosp, Renqiu City, Hebei 062552, Peoples R China [*1]Hebei Med Univ, Dept Oncol, N China Petr Bur Gen Hosp, 8 Huizhan Ave, Renqiu City, Hebei 062552, Peoples R China
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