Continuous 5-fluorouracil infusion plus long acting octreotide in advanced well-differentiated neuroendocrine carcinomas. A phase II trial of the Piemonte Oncology Network

被引:51
作者
Brizzi, Maria P. [1 ]
Berruti, Alfredo [1 ]
Ferrero, Anna [1 ]
Milanesi, Enrica [2 ]
Volante, Marco [1 ]
Castiglione, Federico [3 ]
Birocco, Nadia [2 ]
Bombaci, Sebastiano [4 ]
Perroni, Davide [5 ]
Ferretti, Benedetta [6 ]
Alabiso, Oscar [7 ]
Ciuffreda, Libero [2 ]
Bertetto, Oscar [2 ]
Papotti, Mauro [1 ]
Dogliotti, Luigi [1 ]
机构
[1] Univ Turin, Azienda Osped San Luigi, Dipartimento Sci Clin & Biol, I-10043 Orbassano, TO, Italy
[2] Azienda Osped Molinette, Ctr Oncol Ematol Subalpino, I-10126 Turin, Italy
[3] Osped San Lazzaro, I-12051 Alba, CN, Italy
[4] Osped Ivrea, I-10015 Ivrea, TO, Italy
[5] Osped Civile Saluzzo, I-12037 Saluzzo, CN, Italy
[6] Osped B Eustacchio, I-62027 San Severino Marc, MC, Italy
[7] Azienda Osped Maggiore Carita, I-28100 Novara, Italy
关键词
SOMATOSTATIN ANALOGS; ANTITUMOR-ACTIVITY; BREAST-CANCER; TUMORS; THERAPY; CYCLOPHOSPHAMIDE; FLUOROURACIL; COMBINATION; DIAGNOSIS; SYSTEM;
D O I
10.1186/1471-2407-9-388
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Well-differentiated neuroendocrine carcinomas are highly vascularized and may be sensitive to drugs administered on a metronomic schedule that has shown antiangiogenic properties. A phase II study was designed to test the activity of protracted 5-fluorouracil (5FU) infusion plus long-acting release (LAR) octreotide in patients with neuroendocrine carcinoma. Methods: Twenty-nine patients with metastatic or locally advanced well-differentiated neuroendocrine carcinoma were treated with protracted 5FU intravenous infusion (200 mg/m(2) daily) plus LAR octreotide (20 mg monthly). Patients were followed for toxicity, objective response, symptomatic and biochemical response, time to progression and survival. Results: Assessment by Response Evaluation Criteria in Solid Tumors (RECIST) criteria showed partial response in 7 (24.1%), stable disease in 20 (69.0%), and disease progression in 2 patients. Response did not significantly differ when patients were stratified by primary tumor site and proliferative activity. A biochemical (chromogranin A) response was observed in 12/25 assessable patients (48.0%); symptom relief was obtained in 9/15 symptomatic patients (60.0%). There was non significant decrease in circulating vascular epithelial growth factor (VEGF) over time. Median time to progression was 22.6 months (range, 2.7-68.5); median overall survival was not reached yet. Toxicity was mild and manageable. Conclusion: Continuous/metronomic 5FU infusion plus LAR octreotide is well tolerated and shows activity in patients with well-differentiated neuroendocrine carcinoma. The potential synergism between metronomic chemotherapy and antiangiogenic drugs provides a rationale for exploring this association in the future.
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页数:8
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