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Erschienen in: Journal of Gastrointestinal Cancer 3/2015

01.09.2015 | Letter to the Editor

Sustained Disease Control with TOMOXIRI Regimen in a Patient with Metastatic Pancreatic Adenocarcinoma

verfasst von: Sara De Dosso, Patrizia Melchiorre, Chiara Della Badia, Giorgio Moschovitis, Piercarlo Saletti

Erschienen in: Journal of Gastrointestinal Cancer | Ausgabe 3/2015

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Excerpt

Pancreatic adenocarcinoma (PAC) is one of the most aggressive cancers, and effective systemic treatment is crucial for the management of metastatic disease. Gemcitabine has been considered the standard of care since 1997 [1]. More recently, a randomized phase III trial involving 336 previously untreated metastatic PAC patients compared folinic acid, fluorouracil, irinotecan, oxaliplatin (FOLFIRINOX) regimen with gemcitabine [2]. Overall results revealed that the triplet was superior to gemcitabine in terms of overall survival (OS, 11.1 vs 6.8 months, HR = 0.57, p = .0001), progression-free survival (6.4 vs 3.3 months, p = .001), and response rate (RR, 31.6 vs 9.4 %, p = .0001), with the expense of excess toxicity in the experimental arm. Based on these findings, FOLFIRINOX is considered a reasonable option in first line in patients with good performance status and nearly normal bilirubin, besides emerging combinations such as the doublet gemcitabine and nab-paclitaxel [3]. …
Literatur
1.
Zurück zum Zitat Burris HA, Moore MJ, Andersen J, et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J Clin Oncol. 1997;15:2403–13.PubMed Burris HA, Moore MJ, Andersen J, et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J Clin Oncol. 1997;15:2403–13.PubMed
2.
Zurück zum Zitat Conroy T, Desseigne F, Ychou M, et al. FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer. N Engl J Med. 2011;364:1817–25.PubMedCrossRef Conroy T, Desseigne F, Ychou M, et al. FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer. N Engl J Med. 2011;364:1817–25.PubMedCrossRef
3.
Zurück zum Zitat Von Hoff DD, Ervin T, Arena FP, et al. Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N Engl J Med. 2013;369:1691–703.CrossRef Von Hoff DD, Ervin T, Arena FP, et al. Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N Engl J Med. 2013;369:1691–703.CrossRef
4.
Zurück zum Zitat Saif MW, Shah MM, Shah AR. Fluoropyrimidine-associated cardiotoxicity: revisited. Expert Opin Drug Saf. 2009;8:191–202.PubMedCrossRef Saif MW, Shah MM, Shah AR. Fluoropyrimidine-associated cardiotoxicity: revisited. Expert Opin Drug Saf. 2009;8:191–202.PubMedCrossRef
5.
Zurück zum Zitat Maroun JA, Jonker D, Seymour L, et al. A national cancer institute of Canada clinical trials group study–IND.135: phase I/II study of irinotecan (camptosar), Oxaliplatin and raltitrexed (tomudex) (COT) in patients with advanced colorectal cancer. Eur J Cancer. 2006;42:193–9.PubMedCrossRef Maroun JA, Jonker D, Seymour L, et al. A national cancer institute of Canada clinical trials group study–IND.135: phase I/II study of irinotecan (camptosar), Oxaliplatin and raltitrexed (tomudex) (COT) in patients with advanced colorectal cancer. Eur J Cancer. 2006;42:193–9.PubMedCrossRef
6.
Zurück zum Zitat Kosmas C, Kallistratos M, Kopterides P, et al. Cardiotoxicity of fluoropyrimidines in different schedules of administration: a prospective study. J Cancer Res Clin Oncol. 2008;134:75–82.PubMedCrossRef Kosmas C, Kallistratos M, Kopterides P, et al. Cardiotoxicity of fluoropyrimidines in different schedules of administration: a prospective study. J Cancer Res Clin Oncol. 2008;134:75–82.PubMedCrossRef
7.
Zurück zum Zitat Robben NC, Pippas AW, Moore JO. The syndrome of 5-fluorouracil cardiotoxicity: an elusive cardiopathy. Cancer. 1993;71:493–509.PubMedCrossRef Robben NC, Pippas AW, Moore JO. The syndrome of 5-fluorouracil cardiotoxicity: an elusive cardiopathy. Cancer. 1993;71:493–509.PubMedCrossRef
8.
Zurück zum Zitat Bathina JD, Yusuf SW. 5-fluorouracil-induced coronary vasospasm. J Cardiovasc Med. 2010;11:281–4.CrossRef Bathina JD, Yusuf SW. 5-fluorouracil-induced coronary vasospasm. J Cardiovasc Med. 2010;11:281–4.CrossRef
9.
Zurück zum Zitat Shoemaker LK, Arora U, Rocha Lima CM. 5-fluorouracil-induced coronary vasospasm. Cancer Control. 2004;11:46–9.PubMed Shoemaker LK, Arora U, Rocha Lima CM. 5-fluorouracil-induced coronary vasospasm. Cancer Control. 2004;11:46–9.PubMed
10.
Zurück zum Zitat Luwaert RJ, Descamps O, Majois F, et al. Coronary artery spasm induced by 5-fluorouracil. Eur Heart J. 1991;12:468–70.PubMed Luwaert RJ, Descamps O, Majois F, et al. Coronary artery spasm induced by 5-fluorouracil. Eur Heart J. 1991;12:468–70.PubMed
11.
Zurück zum Zitat Alter P, Herzum M, Soufi Jr M, et al. Cardiotoxicity of 5-fluorouracil. Cardiovasc Hematol Agents Med Chem. 2006;4:1–5.PubMedCrossRef Alter P, Herzum M, Soufi Jr M, et al. Cardiotoxicity of 5-fluorouracil. Cardiovasc Hematol Agents Med Chem. 2006;4:1–5.PubMedCrossRef
12.
Zurück zum Zitat Mosseri M, Fingert HJ, Varticovski L, et al. In vitro evidence that myocardial ischemia resulting from 5-fluorouracil chemotherapy is due to protein kinase C-mediated vasoconstriction of vascular smooth muscle. Cancer Res. 1993;53:3028–33.PubMed Mosseri M, Fingert HJ, Varticovski L, et al. In vitro evidence that myocardial ischemia resulting from 5-fluorouracil chemotherapy is due to protein kinase C-mediated vasoconstriction of vascular smooth muscle. Cancer Res. 1993;53:3028–33.PubMed
13.
Zurück zum Zitat Kelly C, Bhuva N, Harrison M, et al. Use of raltitrexed as an alternative to 5-fluorouracil and capecitabine in cancer patients with cardiac history. Eur J Cancer. 2013;49:2303–10.PubMedCrossRef Kelly C, Bhuva N, Harrison M, et al. Use of raltitrexed as an alternative to 5-fluorouracil and capecitabine in cancer patients with cardiac history. Eur J Cancer. 2013;49:2303–10.PubMedCrossRef
14.
Zurück zum Zitat Ransom D, Wilson K, Fournier M. Final results of Australasian gastrointestinal trials group ARCTIC study: an audit of raltitrexed for patients with cardiac toxicity induced by fluoropyrimidines. Ann Oncol. 2014;25:117–21.PubMedCrossRef Ransom D, Wilson K, Fournier M. Final results of Australasian gastrointestinal trials group ARCTIC study: an audit of raltitrexed for patients with cardiac toxicity induced by fluoropyrimidines. Ann Oncol. 2014;25:117–21.PubMedCrossRef
15.
Zurück zum Zitat Maughan TS, James RD, Kerr DJ, et al. Comparison of survival, palliation, and quality of life with three chemotherapy regimens in metastatic colorectal cancer: a multicentre randomised trial. Lancet. 2002;359:1555–63.PubMedCrossRef Maughan TS, James RD, Kerr DJ, et al. Comparison of survival, palliation, and quality of life with three chemotherapy regimens in metastatic colorectal cancer: a multicentre randomised trial. Lancet. 2002;359:1555–63.PubMedCrossRef
16.
Zurück zum Zitat Francois E, Hebbar M, Bennouna J, et al. A phase II trial of raltitrexed (Tomudex) in advanced pancreatic and biliary tract carcinoma. Oncology. 2005;68:299–305.PubMedCrossRef Francois E, Hebbar M, Bennouna J, et al. A phase II trial of raltitrexed (Tomudex) in advanced pancreatic and biliary tract carcinoma. Oncology. 2005;68:299–305.PubMedCrossRef
17.
Zurück zum Zitat Kralidis E, Aebi S, Friess H, et al. Activity of raltitrexed and gemcitabine in advanced pancreatic cancer. Ann Oncol. 2003;14:574–9.PubMedCrossRef Kralidis E, Aebi S, Friess H, et al. Activity of raltitrexed and gemcitabine in advanced pancreatic cancer. Ann Oncol. 2003;14:574–9.PubMedCrossRef
18.
Zurück zum Zitat Van Laethem JL, Van Maele P, Verslype C, et al. Raltirexed plus gemcitabine (TOMGEM) in advanced pancreatic cancer. Results of a Belgian multicentre phase II study. Oncology. 2004;67:338–43.PubMedCrossRef Van Laethem JL, Van Maele P, Verslype C, et al. Raltirexed plus gemcitabine (TOMGEM) in advanced pancreatic cancer. Results of a Belgian multicentre phase II study. Oncology. 2004;67:338–43.PubMedCrossRef
19.
Zurück zum Zitat Aschele C, Baido C, Sobrero AF, et al. Schedule-dependent synergism between raltitrexed and irinotecan in human colon cancer cells in vitro. Clin Cancer Res. 1998;4:1323–30.PubMed Aschele C, Baido C, Sobrero AF, et al. Schedule-dependent synergism between raltitrexed and irinotecan in human colon cancer cells in vitro. Clin Cancer Res. 1998;4:1323–30.PubMed
20.
Zurück zum Zitat Ford HE, Cunningham D, Ross PJ, et al. Phase I study of irinotecan and raltitrexed in patients with advanced gastrointestinal tract adenocarcinoma. Br J Cancer. 2000;83:146–52.PubMedCentralPubMedCrossRef Ford HE, Cunningham D, Ross PJ, et al. Phase I study of irinotecan and raltitrexed in patients with advanced gastrointestinal tract adenocarcinoma. Br J Cancer. 2000;83:146–52.PubMedCentralPubMedCrossRef
21.
Zurück zum Zitat Ulrich-Pur H, Raderer M, Verena Kornek G, et al. Irinotecan plus raltitrexed vs raltitrexed alone in patients with gemcitabine-pretreated advanced pancreatic adenocarcinoma. Br J Cancer. 2003;88:1180–4.PubMedCentralPubMedCrossRef Ulrich-Pur H, Raderer M, Verena Kornek G, et al. Irinotecan plus raltitrexed vs raltitrexed alone in patients with gemcitabine-pretreated advanced pancreatic adenocarcinoma. Br J Cancer. 2003;88:1180–4.PubMedCentralPubMedCrossRef
22.
Zurück zum Zitat Reni M, Pasetto L, Aprile G, et al. Raltitrexed-eloxatin salvage chemotherapy in gemcitabine-resistant metastatic pancreatic cancer. Br J Cancer. 2006;94:785–91.PubMedCentralPubMedCrossRef Reni M, Pasetto L, Aprile G, et al. Raltitrexed-eloxatin salvage chemotherapy in gemcitabine-resistant metastatic pancreatic cancer. Br J Cancer. 2006;94:785–91.PubMedCentralPubMedCrossRef
Metadaten
Titel
Sustained Disease Control with TOMOXIRI Regimen in a Patient with Metastatic Pancreatic Adenocarcinoma
verfasst von
Sara De Dosso
Patrizia Melchiorre
Chiara Della Badia
Giorgio Moschovitis
Piercarlo Saletti
Publikationsdatum
01.09.2015
Verlag
Springer US
Erschienen in
Journal of Gastrointestinal Cancer / Ausgabe 3/2015
Print ISSN: 1941-6628
Elektronische ISSN: 1941-6636
DOI
https://doi.org/10.1007/s12029-015-9705-4

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