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Ⅲa期非小细胞肺癌术后辅助治疗的临床应用

BACKGROUND AND OBJECTIVE: The efficacy of complete resection of the cancer for patients with stage Ⅲa non-small cell lung cancer (NSCLC) is limited. Synthetic therapy is taken the lead in advocating at present. However, the value of post-operative radiotherapy is not still clear. The aim of this stu...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000425/
https://www.ncbi.nlm.nih.gov/pubmed/20677565
http://dx.doi.org/10.3779/j.issn.1009-3419.2010.04.17
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description BACKGROUND AND OBJECTIVE: The efficacy of complete resection of the cancer for patients with stage Ⅲa non-small cell lung cancer (NSCLC) is limited. Synthetic therapy is taken the lead in advocating at present. However, the value of post-operative radiotherapy is not still clear. The aim of this study is to evaluate the survival time and side effects of postoperative chemotherapy or chemoradiotherapy in the treatment of stage Ⅲa NSCLC. METHODS: Between December 2003 and June 2007, 52 cases that have completed followed-up data with stage Ⅲa of NSCLC received in the First Affiliated Hospital of Dalian Medical University. Twenty-three patients received postoperative chemoradiotherapy (group A) and 29 patients received postoperative chemotherapy combined with radiotherapy (group B). Group A adopted platinum-based combination chemotherapy for 4-6 cycles. The chemotherapeutics included gemcitabine, vinorelbine and docetaxel. Group B used chemotherapy for 2-4 cycles and then received 3-dimensional conformal radiotherapy (3D-CRT). The prescribe dose of target volume was 50 Gy. The chemotherapy was same as for group A and needed 4 cycles in all. The impact of postoperative adjuvant treatment on survival and toxicity was observed in patients with stage Ⅲa NSCLC and the reason of disease progression was analyzed. RESULTS: The median survival was 32.5 months in group A and 31.9 months in group B (P=0.371). Progression-free survival extended about 6 months (P=0.044). The survival rate was 87% at 1 year, 0.1% at 2 year, 33% at 3 year for group A compared with 93%, 69%, 45% for group B. The major side effects were hematological and gastrointestinal toxicities, including nausea, vomiting and neutropenia. There was no significant difference in these toxicities between the two groups (P > 0.05). Radioactive esophageal infection occurred in 17.2% of the patients. Acute and late radioactive lung infection occurred in 13.8% and 27.6% of the patients. All these toxicities were below degree 2. Distant metastases were the main reason of disease progression. There was no significant difference in the rates of local recurrence and metastases between the two groups (P > 0.05). CONCLUSION: Combined modality therapy should be the main therapy of stage Ⅲa NSCLC. The addition of radiotherapy can effectively prolong progression-free survival and don't highly increase the toxicities.
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spelling pubmed-60004252018-07-06 Ⅲa期非小细胞肺癌术后辅助治疗的临床应用 Zhongguo Fei Ai Za Zhi 临床经验 BACKGROUND AND OBJECTIVE: The efficacy of complete resection of the cancer for patients with stage Ⅲa non-small cell lung cancer (NSCLC) is limited. Synthetic therapy is taken the lead in advocating at present. However, the value of post-operative radiotherapy is not still clear. The aim of this study is to evaluate the survival time and side effects of postoperative chemotherapy or chemoradiotherapy in the treatment of stage Ⅲa NSCLC. METHODS: Between December 2003 and June 2007, 52 cases that have completed followed-up data with stage Ⅲa of NSCLC received in the First Affiliated Hospital of Dalian Medical University. Twenty-three patients received postoperative chemoradiotherapy (group A) and 29 patients received postoperative chemotherapy combined with radiotherapy (group B). Group A adopted platinum-based combination chemotherapy for 4-6 cycles. The chemotherapeutics included gemcitabine, vinorelbine and docetaxel. Group B used chemotherapy for 2-4 cycles and then received 3-dimensional conformal radiotherapy (3D-CRT). The prescribe dose of target volume was 50 Gy. The chemotherapy was same as for group A and needed 4 cycles in all. The impact of postoperative adjuvant treatment on survival and toxicity was observed in patients with stage Ⅲa NSCLC and the reason of disease progression was analyzed. RESULTS: The median survival was 32.5 months in group A and 31.9 months in group B (P=0.371). Progression-free survival extended about 6 months (P=0.044). The survival rate was 87% at 1 year, 0.1% at 2 year, 33% at 3 year for group A compared with 93%, 69%, 45% for group B. The major side effects were hematological and gastrointestinal toxicities, including nausea, vomiting and neutropenia. There was no significant difference in these toxicities between the two groups (P > 0.05). Radioactive esophageal infection occurred in 17.2% of the patients. Acute and late radioactive lung infection occurred in 13.8% and 27.6% of the patients. All these toxicities were below degree 2. Distant metastases were the main reason of disease progression. There was no significant difference in the rates of local recurrence and metastases between the two groups (P > 0.05). CONCLUSION: Combined modality therapy should be the main therapy of stage Ⅲa NSCLC. The addition of radiotherapy can effectively prolong progression-free survival and don't highly increase the toxicities. 中国肺癌杂志编辑部 2010-04-20 /pmc/articles/PMC6000425/ /pubmed/20677565 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.04.17 Text en 版权所有©《中国肺癌杂志》编辑部2010 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 临床经验
Ⅲa期非小细胞肺癌术后辅助治疗的临床应用
title Ⅲa期非小细胞肺癌术后辅助治疗的临床应用
title_full Ⅲa期非小细胞肺癌术后辅助治疗的临床应用
title_fullStr Ⅲa期非小细胞肺癌术后辅助治疗的临床应用
title_full_unstemmed Ⅲa期非小细胞肺癌术后辅助治疗的临床应用
title_short Ⅲa期非小细胞肺癌术后辅助治疗的临床应用
title_sort ⅲa期非小细胞肺癌术后辅助治疗的临床应用
topic 临床经验
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000425/
https://www.ncbi.nlm.nih.gov/pubmed/20677565
http://dx.doi.org/10.3779/j.issn.1009-3419.2010.04.17
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