Hochster Howard, Chachoua Abraham, Speyer James, Escalon Juliette, Zeleniuch-Jacquotte Anne, Muggia Franco
NYU School of Medicine, 160 East 32nd St, New York, NY 10016, USA.
J Clin Oncol. 2003 Jul 15;21(14):2703-7. doi: 10.1200/JCO.2003.02.071.
To determine the activity of biweekly oxaliplatin, combined with weekly bolus fluorouracil (FU) and low-dose leucovorin (LV) chemotherapy (bFOL), as first-line therapy for patients with metastatic colorectal cancer.
Patients with measurable metastatic colorectal cancer; no previous therapy for advanced disease (adjuvant therapy allowed if >6 months since completion); and performance status 0, 1, or 2 were eligible and were treated with oxaliplatin 85 mg/m2 days 1 and 15 plus LV 20 mg/m2 over 10 to 20 minutes, followed by a 500 mg/m2 bolus dose of FU on days 1, 8, and 15 every 28 days. Patients underwent response evaluation by computed tomographic scan every 2 months.
Forty-two patients were entered, and 41 patients were treated, including 20 men and 22 women, nine with previous adjuvant chemotherapy and four with radiation therapy. Three patients achieved complete response, and 23 patients achieved partial response, for a response rate of 63% (95% CI, 49% to 78%). Major toxicities included cumulative neuropathy grade 2 (24%) and grade 3 (12%; requiring discontinuation of oxaliplatin), diarrhea grade 3 to 4 (29%) and grade 3 to 4 hematologic toxicity (10%). Median time to progression was 9.0 months (95% confidence interval, 7.1 to 10.8 months) with median survival of 15.9 months (95% confidence interval, 11.4 to 19.7 months).
The bFOL regimen seems to have activity comparable to be infusional programs of FU combined with oxaliplatin. Prospective trials are warranted to determine the relative merits of this schedule compared with the currently indicated schedules.
确定每两周一次的奥沙利铂联合每周一次大剂量氟尿嘧啶(FU)和低剂量亚叶酸钙(LV)化疗(bFOL)作为转移性结直肠癌患者一线治疗方案的活性。
患有可测量的转移性结直肠癌患者;既往未接受过晚期疾病治疗(若完成辅助治疗超过6个月则允许);且体能状态为0、1或2的患者符合条件,接受奥沙利铂85mg/m²,于第1天和第15天给药,同时LV 20mg/m²在10至20分钟内静脉滴注,随后每28天在第1、8和15天给予500mg/m²大剂量FU。患者每2个月通过计算机断层扫描进行疗效评估。
42例患者入组,41例患者接受治疗,其中男性20例,女性22例,9例曾接受辅助化疗,4例曾接受放疗。3例患者达到完全缓解,23例患者达到部分缓解,缓解率为63%(95%CI,49%至78%)。主要毒性包括2级累积神经病变(24%)和3级(12%;需要停用奥沙利铂)、3至4级腹泻(29%)和3至4级血液学毒性(10%)。中位疾病进展时间为9.0个月(95%置信区间,7.1至10.8个月),中位生存期为15.9个月(95%置信区间,11.4至19.7个月)。
bFOL方案似乎具有与FU联合奥沙利铂的输注方案相当的活性。有必要进行前瞻性试验以确定该方案与当前推荐方案相比的相对优势。