Vinorelbine and 5-Fluorouracil Bolus and/or Continuous Venous Infusion Plus Levofolinic Acid as Second-line Chemotherapy for Metastatic Breast Cancer: an Analysis of Results in Clinical Practice of the Gruppo Oncologico Italia Meridionale (GOIM)
Background: This retrospective study evaluated the activity and toxicity profile of a regimen of vinorelbine and 5-fluorouracil with levofolinic acid, given to a large series of patients with recurrent or refractory metastatic breast cancer after first-line chemotherapy. Patients and Methods: Overal...
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Published in | Anticancer research Vol. 26; no. 4B; pp. 3143 - 3150 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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International Institute of Anticancer Research
01.07.2006
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Abstract | Background: This retrospective study evaluated the activity and toxicity profile of a regimen of vinorelbine and 5-fluorouracil
with levofolinic acid, given to a large series of patients with recurrent or refractory metastatic breast cancer after first-line
chemotherapy. Patients and Methods: Overall, 286 evaluable patients were included in the analysis. Two chemotherapy schedules
were reviewed: a) the bolus regimen consisted of levofolinic acid 100 mg/m 2 and 5-fluorouracil 375 mg/m 2 , both administered i.v. on days 1,2 and 3, plus vinorelbine 25 mg/m 2 i.v. bolus on days 1 and 8 every 3 weeks; b) the infusional regimen of levofolinic acid 100 mg/m 2 given as a 2-hour infusion, followed by 5-fluorouracil 400 mg/m 2 i.v. bolus and by 5-fluorouracil 600 mg/m 2 administered as 22-hour continuous venous infusion (c.v.i) for 2 days, plus vinorelbine i.v. bolus on days 1 and 8. Results:
Overall, twelve patients achieved a complete response (4%; 95%CL 2%-7%) and 115 patients showed a partial response (40%, 95%CL
34%-46%), for an overall response rate of 44% (95CL 39%-50%). Sixty-one patients had stable disease (21%) and 98 patients
progressive disease (34%). The tumor growth control rate was 63% (95%CL 60%-71%). Patients with soft tissue metastases as
the dominant disease showed the highest response rate (56%), followed by viscera (48%) and bone (33%). The difference in response
rate between patients with dominant visceral disease versus those with dominant bone disease was statistically significant
(p=0.038). Patients treated with the bolus schedule achieved a 40% overall response rate with a 5% complete response rate,
while those who received the infusional regimen had a 48% overall response rate with a 5% complete response rate. This difference
was not statistically significant (p=0.164). The overall median duration of objective responses was 8.3 months (range 4-14
months), median time to progression of the all series was 6.1 months (range 2-24 months) and the median overall survival was
14.6 months (range 3-32). There was a statistically significant difference in survival among responder and non-responder patients
(p=0.0009). Conclusion: The results of this large off-trial analysis confirmed the clinical activity and adverse-event profile
reported in controlled clinical trials of the vinorelbine/ 5-fluorouracil with levofolinic acid regimen in clinical practice.
This combination regimen was active with a low toxicity burden and, therefore, represents a good therapeutic choice for patients
who require second-line chemotherapy. |
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AbstractList | Background: This retrospective study evaluated the activity and toxicity profile of a regimen of vinorelbine and 5-fluorouracil
with levofolinic acid, given to a large series of patients with recurrent or refractory metastatic breast cancer after first-line
chemotherapy. Patients and Methods: Overall, 286 evaluable patients were included in the analysis. Two chemotherapy schedules
were reviewed: a) the bolus regimen consisted of levofolinic acid 100 mg/m 2 and 5-fluorouracil 375 mg/m 2 , both administered i.v. on days 1,2 and 3, plus vinorelbine 25 mg/m 2 i.v. bolus on days 1 and 8 every 3 weeks; b) the infusional regimen of levofolinic acid 100 mg/m 2 given as a 2-hour infusion, followed by 5-fluorouracil 400 mg/m 2 i.v. bolus and by 5-fluorouracil 600 mg/m 2 administered as 22-hour continuous venous infusion (c.v.i) for 2 days, plus vinorelbine i.v. bolus on days 1 and 8. Results:
Overall, twelve patients achieved a complete response (4%; 95%CL 2%-7%) and 115 patients showed a partial response (40%, 95%CL
34%-46%), for an overall response rate of 44% (95CL 39%-50%). Sixty-one patients had stable disease (21%) and 98 patients
progressive disease (34%). The tumor growth control rate was 63% (95%CL 60%-71%). Patients with soft tissue metastases as
the dominant disease showed the highest response rate (56%), followed by viscera (48%) and bone (33%). The difference in response
rate between patients with dominant visceral disease versus those with dominant bone disease was statistically significant
(p=0.038). Patients treated with the bolus schedule achieved a 40% overall response rate with a 5% complete response rate,
while those who received the infusional regimen had a 48% overall response rate with a 5% complete response rate. This difference
was not statistically significant (p=0.164). The overall median duration of objective responses was 8.3 months (range 4-14
months), median time to progression of the all series was 6.1 months (range 2-24 months) and the median overall survival was
14.6 months (range 3-32). There was a statistically significant difference in survival among responder and non-responder patients
(p=0.0009). Conclusion: The results of this large off-trial analysis confirmed the clinical activity and adverse-event profile
reported in controlled clinical trials of the vinorelbine/ 5-fluorouracil with levofolinic acid regimen in clinical practice.
This combination regimen was active with a low toxicity burden and, therefore, represents a good therapeutic choice for patients
who require second-line chemotherapy. This retrospective study evaluated the activity and toxicity profile of a regimen of vinorelbine and 5-fluorouracil with levofolinic acid, given to a large series of patients with recurrent or refractory metastatic breast cancer after first-line chemotherapy. Overall, 286 evaluable patients were included in the analysis. Two chemotherapy schedules were reviewed: a) the bolus regimen consisted of levofolinic acid 100 mg/m2 and 5-fluorouracil 375 mg/m2, both administered i.v. on days 1,2 and 3, plus vinorelbine 25 mg/m2 i.v. bolus on days 1 and 8 every 3 weeks; b) the infusional regimen of levofolinic acid 100 mg/m2 given as a 2-hour infusion, followed by 5-fluorouracil 400 mg/m2 i.v. bolus and by 5-fluorouracil 600 mg/m2 administered as 22-hour continuous venous infusion (c.v.i) for 2 days, plus vinorelbine i.v. bolus on days 1 and 8. Overall, twelve patients achieved a complete response (4%; 95%CL 2%-7%) and 115 patients showed a partial response (40%, 95%CL 34%-46%), for an overall response rate of 44% (95CL 39%-50%). Sixty-one patients had stable disease (21%) and 98 patients progressive disease (34%). The tumor growth control rate was 63% (95%CL 60%-71%). Patients with soft tissue metastases as the dominant disease showed the highest response rate (56%), followed by viscera (48%) and bone (33%). The difference in response rate between patients with dominant visceral disease versus those with dominant bone disease was statistically significant (p=0.038). Patients treated with the bolus schedule achieved a 40% overall response rate with a 5% complete response rate, while those who received the infusional regimen had a 48% overall response rate with a 5% complete response rate. This difference was not statistically significant (p=0.164). The overall median duration of objective responses was 8.3 months (range 4-14 months), median time to progression of the all series was 6.1 months (range 2-24 months) and the median overall survival was 14.6 months (range 3-32). There was a statistically significant difference in survival among responder and non-responder patients (p=0.0009). The results of this large off-trial analysis confirmed the clinical activity and adverse-event profile reported in controlled clinical trials of the vinorelbine/ 5-fluorouracil with levofolinic acid regimen in clinical practice. This combination regimen was active with a low toxicity burden and, therefore, represents a good therapeutic choice for patients who require second-line chemotherapy. |
Author | FRANCESCA VARVARA EUGENIA BAJARDI MICHELE CARUSO NICOLÃ BORSELLINO MAURIZIO CHIARENZA VITTORIO GEBBIA PAOLO TRALONGO ROBERTO VALENZA ANTONIO MARRAZZO FRANCESCO FERRAÃ ROSANNA AJELLO FRANCESCO VERDERAME MARIA LINA TIRRITO ROBERTO BORDONARO |
Author_xml | – sequence: 1 givenname: Vittorio surname: GEBBIA fullname: GEBBIA, Vittorio organization: Department of Experimental Oncology and Clinical Application, University of Palermo, Italy – sequence: 2 givenname: Michele surname: CARUSO fullname: CARUSO, Michele organization: Medical Oncology Unit, Centro Catanese di Oncologia, Catania, Italy – sequence: 3 givenname: Eugenia surname: BAJARDI fullname: BAJARDI, Eugenia organization: Medical Oncology Unit, La Maddalena Clinic for Cancer, Palermo, Italy – sequence: 4 givenname: Francesco surname: FERRAU fullname: FERRAU, Francesco organization: Division of Medical Oncology, Ospedale San Vincenzo, Taormina, Italy – sequence: 5 givenname: Roberto surname: BORDONARO fullname: BORDONARO, Roberto organization: Medical Oncology Unit, Ospedale Vittorio Emanuele, Catania, Italy – sequence: 6 givenname: Paolo surname: TRALONGO fullname: TRALONGO, Paolo organization: Medical Oncology Unit, Ospedale De Maria, Avola, Italy – sequence: 7 givenname: Nicolo surname: BORSELLINO fullname: BORSELLINO, Nicolo organization: Division of Medical Oncology, Ospedale Buccheri La Ferla, Palermo, Italy – sequence: 8 givenname: Rosanna surname: AJELLO fullname: AJELLO, Rosanna organization: Medical Oncology Unit, Centro Catanese di Oncologia, Catania, Italy – sequence: 9 givenname: Maria Lina surname: TIRRITO fullname: TIRRITO, Maria Lina organization: Division of Medical Oncology, Casa di Cura Torina, Palermo, Italy – sequence: 10 givenname: Maurizio surname: CHIARENZA fullname: CHIARENZA, Maurizio organization: Service of Medical Oncology, Ospedale Vittorio Emanuele, Gela, Italy – sequence: 11 givenname: Roberto surname: VALENZA fullname: VALENZA, Roberto organization: Service of Medical Oncology, Ospedale Vittorio Emanuele, Gela, Italy – sequence: 12 givenname: Francesco surname: VERDERAME fullname: VERDERAME, Francesco organization: Service of Medical Oncology, Ospedale Civile, Sciacca, Italy – sequence: 13 givenname: Francesca surname: VARVARA fullname: VARVARA, Francesca organization: Service of Oncology, Casa di Cura Villa dei Gerani, Trapani, Italy – sequence: 14 givenname: Antonio surname: MARRAZZO fullname: MARRAZZO, Antonio organization: Department of Experimental Oncology and Clinical Application, University of Palermo, Italy |
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Keywords | Antineoplastic agent Metastasis metastases Alkaloid Cancerology Blood vessel Advanced stage Vein Antimitotic Fluorouracil Enzyme Fluoropyrimidine derivatives Transferases second-line chemotherapy Enzyme inhibitor Breast cancer Malignant tumor Thymidylate synthase Mammary gland diseases Chemotherapy Bolus injection Treatment Antimetabolic Methyltransferases Perfusion Pyrimidine derivatives Circulatory system Vinorelbine |
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Snippet | Background: This retrospective study evaluated the activity and toxicity profile of a regimen of vinorelbine and 5-fluorouracil
with levofolinic acid, given to... This retrospective study evaluated the activity and toxicity profile of a regimen of vinorelbine and 5-fluorouracil with levofolinic acid, given to a large... |
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SubjectTerms | Adult Aged Antineoplastic Combined Chemotherapy Protocols - administration & dosage Antineoplastic Combined Chemotherapy Protocols - adverse effects Biological and medical sciences Breast Neoplasms - drug therapy Breast Neoplasms - pathology Female Fluorouracil - administration & dosage Fluorouracil - adverse effects Gynecology. Andrology. Obstetrics Humans Infusions, Intravenous Injections, Intravenous Leucovorin - administration & dosage Leucovorin - adverse effects Mammary gland diseases Medical sciences Middle Aged Neoplasm Metastasis Neoplasm Recurrence, Local - drug therapy Neoplasm Recurrence, Local - pathology Retrospective Studies Stereoisomerism Tumors Vinblastine - administration & dosage Vinblastine - adverse effects Vinblastine - analogs & derivatives |
Title | Vinorelbine and 5-Fluorouracil Bolus and/or Continuous Venous Infusion Plus Levofolinic Acid as Second-line Chemotherapy for Metastatic Breast Cancer: an Analysis of Results in Clinical Practice of the Gruppo Oncologico Italia Meridionale (GOIM) |
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