{"title":"结直肠癌II期T4肿瘤的临床特征:10年单中心研究报告","authors":"Bo-Zhi Lin, Chang-Lin Lin, Feng-Fan Chiang, Chou-Chen Chen, Ming-Cheng Chen, Chun-Yu Lin, Shang-Chih Huang","doi":"10.3390/curroncol31120584","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>The tumor staging of colorectal cancer (CRC) plays a significant role in both treatment and prognosis, impacting surgical planning and adjuvant therapy decisions. Currently, the staging of CRC is based on the TNM system developed by the American Joint Committee on Cancer. Prior studies have suggested that survival rates and recurrent rates of T4a tumors appear to be worse than that of T4b tumors, although there is currently no consensus. Therefore, we collected patient data from Taichung Veterans General Hospital over the past decade in order to conduct further research.</p><p><strong>Method: </strong>Between 2010 and 2018, a total of 5760 newly diagnosed CRC patients were seen at the hospital. To eliminate the influence of any local lymph node involvement or distant organ metastasis on the research results, we focused on patients with pathologic Stage IIc disease (T4a-bN0M0). Patients with rectal cancer who had received neoadjuvant concurrent chemoradiotherapy were excluded. Ultimately, 132 patients were included in this study. A multivariate Cox regression analysis was conducted to identify independent risk factors for both 10-year cancer-specific survival (CSS) and overall survival (OS).</p><p><strong>Results: </strong>A total of 132 patients were included in the study, with 90 classified as T4a and 42 as T4b. The 10-year CSS for pT4a and pT4b was 72.5% and 56.5%, respectively, with a <i>p</i>-value of 0.011. The 10-year OS for pT4a and pT4b was 48.4% and 42.5%, respectively, with a <i>p</i>-value of 0.086. There was no significant difference in the site of first recurrence between the pT4a and pT4b groups (<i>p</i>-value = 0.936). Overall, patients who received adjuvant chemotherapy therapy had a significantly better prognosis (<i>p</i>-value < 0.05). However, there was no significant difference in prognosis between oral 5-FU and FOLFOX.</p><p><strong>Conclusion: </strong>Based on our data, patients diagnosed with pathologic T4aN0M0 CRC appeared to experience a trend toward better 10-year OS when compared to those with T4bN0M0 disease, but this trend lacks statistical significance. Patients with locally advanced Stage II colon cancer clearly benefited from adjuvant chemotherapy therapy; therefore, FOLFOX may not necessarily be required.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"31 12","pages":"7924-7935"},"PeriodicalIF":2.8000,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11674692/pdf/","citationCount":"0","resultStr":"{\"title\":\"The Clinical Characteristics of a Stage II Colorectal Cancer T4 Tumor: A Ten-Year Single-Center Research Report.\",\"authors\":\"Bo-Zhi Lin, Chang-Lin Lin, Feng-Fan Chiang, Chou-Chen Chen, Ming-Cheng Chen, Chun-Yu Lin, Shang-Chih Huang\",\"doi\":\"10.3390/curroncol31120584\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aim: </strong>The tumor staging of colorectal cancer (CRC) plays a significant role in both treatment and prognosis, impacting surgical planning and adjuvant therapy decisions. Currently, the staging of CRC is based on the TNM system developed by the American Joint Committee on Cancer. Prior studies have suggested that survival rates and recurrent rates of T4a tumors appear to be worse than that of T4b tumors, although there is currently no consensus. Therefore, we collected patient data from Taichung Veterans General Hospital over the past decade in order to conduct further research.</p><p><strong>Method: </strong>Between 2010 and 2018, a total of 5760 newly diagnosed CRC patients were seen at the hospital. To eliminate the influence of any local lymph node involvement or distant organ metastasis on the research results, we focused on patients with pathologic Stage IIc disease (T4a-bN0M0). Patients with rectal cancer who had received neoadjuvant concurrent chemoradiotherapy were excluded. Ultimately, 132 patients were included in this study. A multivariate Cox regression analysis was conducted to identify independent risk factors for both 10-year cancer-specific survival (CSS) and overall survival (OS).</p><p><strong>Results: </strong>A total of 132 patients were included in the study, with 90 classified as T4a and 42 as T4b. The 10-year CSS for pT4a and pT4b was 72.5% and 56.5%, respectively, with a <i>p</i>-value of 0.011. The 10-year OS for pT4a and pT4b was 48.4% and 42.5%, respectively, with a <i>p</i>-value of 0.086. There was no significant difference in the site of first recurrence between the pT4a and pT4b groups (<i>p</i>-value = 0.936). Overall, patients who received adjuvant chemotherapy therapy had a significantly better prognosis (<i>p</i>-value < 0.05). However, there was no significant difference in prognosis between oral 5-FU and FOLFOX.</p><p><strong>Conclusion: </strong>Based on our data, patients diagnosed with pathologic T4aN0M0 CRC appeared to experience a trend toward better 10-year OS when compared to those with T4bN0M0 disease, but this trend lacks statistical significance. Patients with locally advanced Stage II colon cancer clearly benefited from adjuvant chemotherapy therapy; therefore, FOLFOX may not necessarily be required.</p>\",\"PeriodicalId\":11012,\"journal\":{\"name\":\"Current oncology\",\"volume\":\"31 12\",\"pages\":\"7924-7935\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-12-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11674692/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3390/curroncol31120584\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/curroncol31120584","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的:结直肠癌(CRC)的肿瘤分期对治疗和预后均有重要影响,影响手术计划和辅助治疗决策。目前,CRC的分期是基于美国癌症联合委员会(American Joint Committee on Cancer)制定的TNM系统。先前的研究表明,T4a肿瘤的生存率和复发率似乎比T4b肿瘤差,尽管目前尚无共识。因此,我们收集台中退伍军人总医院近十年的病患资料,以作进一步研究。方法:2010年至2018年,本院共收治新诊断的结直肠癌患者5760例。为了消除任何局部淋巴结累及或远处器官转移对研究结果的影响,我们重点研究了病理性IIc期疾病(T4a-bN0M0)患者。同时接受新辅助放化疗的直肠癌患者被排除在外。最终,132名患者被纳入本研究。采用多变量Cox回归分析确定影响10年癌症特异性生存(CSS)和总生存(OS)的独立危险因素。结果:共纳入132例患者,其中T4a级90例,T4b级42例。pT4a和pT4b的10年CSS分别为72.5%和56.5%,p值为0.011。pT4a和pT4b的10年OS分别为48.4%和42.5%,p值为0.086。pT4a组与pT4b组首次复发部位比较差异无统计学意义(p值= 0.936)。总体而言,接受辅助化疗的患者预后明显较好(p值< 0.05)。然而,口服5-FU与FOLFOX的预后无显著差异。结论:根据我们的数据,与T4bN0M0疾病相比,病理性T4aN0M0 CRC患者的10年OS似乎有更好的趋势,但这种趋势缺乏统计学意义。局部晚期II期结肠癌患者明显受益于辅助化疗;因此,FOLFOX可能不一定是必需的。
The Clinical Characteristics of a Stage II Colorectal Cancer T4 Tumor: A Ten-Year Single-Center Research Report.
Aim: The tumor staging of colorectal cancer (CRC) plays a significant role in both treatment and prognosis, impacting surgical planning and adjuvant therapy decisions. Currently, the staging of CRC is based on the TNM system developed by the American Joint Committee on Cancer. Prior studies have suggested that survival rates and recurrent rates of T4a tumors appear to be worse than that of T4b tumors, although there is currently no consensus. Therefore, we collected patient data from Taichung Veterans General Hospital over the past decade in order to conduct further research.
Method: Between 2010 and 2018, a total of 5760 newly diagnosed CRC patients were seen at the hospital. To eliminate the influence of any local lymph node involvement or distant organ metastasis on the research results, we focused on patients with pathologic Stage IIc disease (T4a-bN0M0). Patients with rectal cancer who had received neoadjuvant concurrent chemoradiotherapy were excluded. Ultimately, 132 patients were included in this study. A multivariate Cox regression analysis was conducted to identify independent risk factors for both 10-year cancer-specific survival (CSS) and overall survival (OS).
Results: A total of 132 patients were included in the study, with 90 classified as T4a and 42 as T4b. The 10-year CSS for pT4a and pT4b was 72.5% and 56.5%, respectively, with a p-value of 0.011. The 10-year OS for pT4a and pT4b was 48.4% and 42.5%, respectively, with a p-value of 0.086. There was no significant difference in the site of first recurrence between the pT4a and pT4b groups (p-value = 0.936). Overall, patients who received adjuvant chemotherapy therapy had a significantly better prognosis (p-value < 0.05). However, there was no significant difference in prognosis between oral 5-FU and FOLFOX.
Conclusion: Based on our data, patients diagnosed with pathologic T4aN0M0 CRC appeared to experience a trend toward better 10-year OS when compared to those with T4bN0M0 disease, but this trend lacks statistical significance. Patients with locally advanced Stage II colon cancer clearly benefited from adjuvant chemotherapy therapy; therefore, FOLFOX may not necessarily be required.
期刊介绍:
Current Oncology is a peer-reviewed, Canadian-based and internationally respected journal. Current Oncology represents a multidisciplinary medium encompassing health care workers in the field of cancer therapy in Canada to report upon and to review progress in the management of this disease.
We encourage submissions from all fields of cancer medicine, including radiation oncology, surgical oncology, medical oncology, pediatric oncology, pathology, and cancer rehabilitation and survivorship. Articles published in the journal typically contain information that is relevant directly to clinical oncology practice, and have clear potential for application to the current or future practice of cancer medicine.