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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Chronomodulated chemotherapy in metastatic gastrointestinal cancer combining 5-FU and sodium folinate with oxaliplatin, irinotecan or gemcitabine: the Jena experience in 79 patients.
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Chronomodulated chemotherapy in metastatic gastrointestinal cancer combining 5-FU and sodium folinate with oxaliplatin, irinotecan or gemcitabine: the Jena experience in 79 patients.

机译:5-FU和亚叶酸钠与奥沙利铂,伊立替康或吉西他滨合用的转移性胃肠道癌的定时化疗:耶拿79例的经验。

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PURPOSE. To study efficacy and tolerability of chronomodulated (CM)-chemotherapy in patients with metastatic or locally advanced tumors of the GI tract. Furthermore, calcium folinate was replaced by sodium folinate due to better feasibility. PATIENTS AND METHODS. We treated 79 patients with metastatic or locally advanced colorectal cancer ( n=52), cancer of the pancreas/biliary tract ( n=14), and other malignancies ( n=14) with a total of 592 courses of CM-therapy. Out of the total study population 53/79, i.e., 67.1% had received prior chemotherapy. Most of the patients (77.2%) received sodium-folinate-5-FU-oxaliplatin-CM (SOFOX-CM) as first-line chronomodulated therapy, 20.3% received sodium-folinate-5-FU-irinotecan-CM (SOFIRI-CM), and 2.5% ( n=1) received sodium-folinate-5-FU-gemcitabine-CM (SOFGEM-CM). RESULTS. We found a moderate overall toxicity with grade 3-4 neuropathy in 7.46% of patients during a total of 433 courses of SOFOX-CM and grade 3-4 diarrhea in 10.26% of patients after 154 courses of SOFIRI-CM. SOFOX-CM had to be stopped only in one patient due to grade 3-4 sensory neuropathy. CM-therapy led to complete response (CR) in 1.3%, partial response (PR) in 15.2%, stable disease (SD) in 32.9%, and progressive disease (PD) in 44.3% of all patients. For the 26 chemonaive patients remission data were as follows: CR one patient (3.8%), PR four patients (15.4%), SD seven patients (26.9%), PD 12 patients (46.3%), lost to follow-up one patient (3.8%), and too-early-for-analysis one patient (3.8%). The median progression-free-survival (PFS) was 4 months (range, 0-24 months). The median PFS was also 4 months (range, 0-21 months) for those patients receiving SOFOX-CM as first CM-therapy ( n=61), while it was found to be 0 months (range, 0-10 months) for patients ( n=16) receiving SOFIRI-CM as first chronomodulated therapy. CONCLUSIONS. We found CM-therapy to be effective and safe in the treatment of advanced malignancies of the GI tract. Sodium folinate offers superior feasibility and compatibility with cytostatic drugs without drawbacks.
机译:目的。研究同步化(CM)化学疗法在胃肠道转移性或局部晚期肿瘤患者中的疗效和耐受性。此外,由于更好的可行性,用叶酸钠代替叶酸钙。病人和方法。我们治疗了79例转移性或局部晚期大肠癌(n = 52),胰腺/胆道癌(n = 14)和其他恶性肿瘤(n = 14),共592个疗程的CM治疗。在全部研究人群中,有53/79的人(即67.1%)曾经接受过化疗。大多数患者(77.2%)接受亚叶酸-5-FU-奥沙利铂-CM(SOFOX-CM)作为一线同步治疗,20.3%接受叶酸-5-FU-伊立替康-CM(SOFIRI-CM )和2.5%(n = 1)的人接受亚叶酸-5-FU-吉西他滨-CM(SOFGEM-CM)。结果。我们发现,在总共433个疗程的SOFOX-CM疗程中,有7.46%的患者出现3-4级神经病变的中等毒性,在154个疗程的SOFIRI-CM疗程中,在10.26%的患者中出现3-4级腹泻。由于3-4级感觉神经病,只有一名患者必须停止使用SOFOX-CM。 CM治疗导致所有患者的完全缓解(CR)为1.3%,部分缓解(PR)为15.2%,稳定疾病(SD)为32.9%,进行性疾病(PD)为44.3%。 26例化疗阳性患者的缓解数据如下:CR 1例(3.8%),PR 4例(15.4%),SD 7例(26.9%),PD 12例(46.3%),失去随访1例(3.8%),以及太早需要分析的一名患者(3.8%)。中位无进展生存期(PFS)为4个月(范围0-24个月)。接受SOFOX-CM作为首次CM治疗的患者的PFS中位数也为4个月(0-21个月)(n = 61),而被发现为0个月(0-10个月)的患者。接受SOFIRI-CM作为第一种计时疗法的患者(n = 16)。结论。我们发现CM疗法在胃肠道晚期恶性肿瘤的治疗中是有效和安全的。亚叶酸钠提供了卓越的可行性和与细胞抑制药物的相容性,而没有缺点。

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