Andreas Teufel , Moying Li , Michael Gerken , Matthias P. Ebert , Hans J Schlitt , Matthias Evert , Wolfgang Herr , Monika Klinkhammer-Schalke
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Most frequent second cancers were prostate cancer<span><span> (18.4%), colon cancer (16.1%), breast cancers (8.1%), lung cancer (8.1%), rectal cancer<span> (4.9%) and uterine cancer (4.9%). However, in comparison to non-treated patients this did not represent a significantly increased risk for subsequent second cancer </span></span>in patients after treatment with additive chemotherapy. Of interest, our data suggest a significantly decreased second cancer rate in patients treated with </span></span>FOLFOX compared to FUFOL for additive treatment.</p></div><div><h3>Conclusions</h3><p>Second cancer development was not increased after additive chemotherapy for colon cancer, which is a novel aspect in the ongoing discussions on reduction of adjuvant treatment to 3 months or treatment of lymph node negative patients.</p><p><strong>Novelty and Impact Statement</strong></p><p>To our knowledge, this is the first population-based study analyzing second cancer development after additive chemotherapy in patients with UICC III-IV colon cancer. The results have an important impact on the surveillance and long-term follow-up of cancer patients.</p></div>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Second Cancer After Additive Chemotherapy in Patients With Colon Cancer\",\"authors\":\"Andreas Teufel , Moying Li , Michael Gerken , Matthias P. Ebert , Hans J Schlitt , Matthias Evert , Wolfgang Herr , Monika Klinkhammer-Schalke\",\"doi\":\"10.1016/j.clcc.2022.07.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p><span><span>Additive chemotherapeutic treatment of UICC-stage -III / IV </span>colon cancer<span><span> with fluorouracil, </span>leucovorin and </span></span>oxaliplatin is widely accepted as current standard of treatment after R0-resection. However, as patients.. survival is increasing, long-term side effects of chemotherapeutic agents such as second cancer development are becoming increasingly important.</p></div><div><h3>Patients</h3><p>We therefore investigated a total of 2 856 Patients with UICC-stage III / IV colon cancer, 223 of whom (7.8%) had developed a subsequent second cancer.</p></div><div><h3>Results</h3><p><span>Median follow-up was 73.2 months (range 209.9 months, 95%-CI 69.8-76.9). Most frequent second cancers were prostate cancer<span><span> (18.4%), colon cancer (16.1%), breast cancers (8.1%), lung cancer (8.1%), rectal cancer<span> (4.9%) and uterine cancer (4.9%). However, in comparison to non-treated patients this did not represent a significantly increased risk for subsequent second cancer </span></span>in patients after treatment with additive chemotherapy. 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引用次数: 2
摘要
背景:联合氟尿嘧啶、亚叶酸素和奥沙利铂对uicc -III / IV期结肠癌进行化疗是目前被广泛接受的r0切除术后的标准治疗方法。然而,作为病人…生存率越来越高,化疗药物的长期副作用,如二次癌症的发展变得越来越重要。因此,我们共调查了2856例uicc - III / IV期结肠癌患者,其中223例(7.8%)随后发展为第二种癌症。结果中位随访时间为73.2个月(范围209.9个月,95% ci 69.8-76.9)。其次是前列腺癌(18.4%)、结肠癌(16.1%)、乳腺癌(8.1%)、肺癌(8.1%)、直肠癌(4.9%)和子宫癌(4.9%)。然而,与未接受治疗的患者相比,这并不代表在接受附加化疗治疗后患者发生第二次癌症的风险显着增加。有趣的是,我们的数据表明,与附加治疗的FUFOL相比,FOLFOX治疗的患者第二次癌症发生率显着降低。结论结肠癌加性化疗后二次肿瘤发展未增加,这是目前关于将辅助治疗时间缩短至3个月或淋巴结阴性患者治疗的讨论中的一个新方面。新颖性和影响声明:据我们所知,这是第一个基于人群的研究,分析了UICC III-IV型结肠癌患者在加性化疗后的二次癌症发展。研究结果对癌症患者的监测和长期随访具有重要影响。
Second Cancer After Additive Chemotherapy in Patients With Colon Cancer
Background
Additive chemotherapeutic treatment of UICC-stage -III / IV colon cancer with fluorouracil, leucovorin and oxaliplatin is widely accepted as current standard of treatment after R0-resection. However, as patients.. survival is increasing, long-term side effects of chemotherapeutic agents such as second cancer development are becoming increasingly important.
Patients
We therefore investigated a total of 2 856 Patients with UICC-stage III / IV colon cancer, 223 of whom (7.8%) had developed a subsequent second cancer.
Results
Median follow-up was 73.2 months (range 209.9 months, 95%-CI 69.8-76.9). Most frequent second cancers were prostate cancer (18.4%), colon cancer (16.1%), breast cancers (8.1%), lung cancer (8.1%), rectal cancer (4.9%) and uterine cancer (4.9%). However, in comparison to non-treated patients this did not represent a significantly increased risk for subsequent second cancer in patients after treatment with additive chemotherapy. Of interest, our data suggest a significantly decreased second cancer rate in patients treated with FOLFOX compared to FUFOL for additive treatment.
Conclusions
Second cancer development was not increased after additive chemotherapy for colon cancer, which is a novel aspect in the ongoing discussions on reduction of adjuvant treatment to 3 months or treatment of lymph node negative patients.
Novelty and Impact Statement
To our knowledge, this is the first population-based study analyzing second cancer development after additive chemotherapy in patients with UICC III-IV colon cancer. The results have an important impact on the surveillance and long-term follow-up of cancer patients.