Skip to main content
Top
Published in: Cancer Chemotherapy and Pharmacology 1/2007

01-01-2007 | Original Article

Thalidomide and celecoxib as potential modulators of irinotecan’s activity in cancer patients

Authors: Miguel Villalona-Calero, Larry Schaaf, Gary Phillips, Gregory Otterson, Kevin Panico, Wenrui Duan, Barbara Kleiber, Manisha Shah, Donn Young, Wan-Hong Wu, John Kuhn

Published in: Cancer Chemotherapy and Pharmacology | Issue 1/2007

Login to get access

Abstract

Purpose: Nuclear factor-κB (NF-κB) activation induces resistance to irinotecan. Preclinically, thalidomide and COX-2 inhibitors reduce NF-κB activation. We tested the feasibility of combining irinotecan with thalidomide and thalidomide/celecoxib in patients with refractory malignancies. Patients/methods: The study was conducted in two parts. First, the optimal dose of thalidomide (400 or 200 mg daily) in combination with irinotecan 125 mg/m2 days 1 and 8 every 3 weeks was determined. In the second part, celecoxib 400 mg twice-daily was added to irinotecan/thalidomide. Pharmacokinetics of irinotecan and thalidomide alone or concurrently were evaluated. Tumor necrosis factor alpha, beta-fibroblast growth factor, and NF-κB activation were measured in blood mononuclear cells (PBMC). No CYP450 enzyme inducers/inhibitors were allowed. Results: Thirty-six patients were enrolled: Eleven received thalidomide 400 mg, 13 thalidomide 200 mg and 12 thalidomide 400 mg and celecoxib, with irinotecan. For the two-drug combination, there was a higher rate of moderate/severe diarrhea/myelosuppression with thalidomide 200 mg. Thus thalidomide 400 mg was combined with celecoxib. The triple combination resulted in similar toxicity as the doublet with the lower thalidomide dose. Concurrent administration of irinotecan/thalidomide did not influence pharmacokinetics. Anti-tumor responses occurred in two patients and prolonged stabilization in eight others. NF-κB activation increased over time. Patients experiencing tumor response or prolonged stabilization had lower NF-κB activation, albeit not statistically significant (P = 0.124). Conclusions: The combination of thalidomide/irinotecan is safe and devoid of PK interactions. Thalidomide 400 mg appeared more suitable for combination, whereas the addition of celecoxib did not improve tolerability. Tumor-specific studies in patients with lesser prior treatment will be necessary to establish the therapeutic impact of the combinations.
Literature
1.
go back to reference Hsiang YH, Liu LF (1988) Identification of mammalian DNA topoisomerase I as an intracellular target of the anticancer drug camptothecin. Cancer Res 48:1722–1726PubMed Hsiang YH, Liu LF (1988) Identification of mammalian DNA topoisomerase I as an intracellular target of the anticancer drug camptothecin. Cancer Res 48:1722–1726PubMed
2.
go back to reference Douillard JY, Cunningham D, Roth AD et al (2000) Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicentre randomised trial. Lancet 355:1041–1047PubMedCrossRef Douillard JY, Cunningham D, Roth AD et al (2000) Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicentre randomised trial. Lancet 355:1041–1047PubMedCrossRef
3.
go back to reference Ilson DH, Saltz L, Enzinger P et al (1999) Phase II trial of weekly irinotecan plus cisplatin in advanced esophageal cancer. J Clin Oncol 17:3270–3275PubMed Ilson DH, Saltz L, Enzinger P et al (1999) Phase II trial of weekly irinotecan plus cisplatin in advanced esophageal cancer. J Clin Oncol 17:3270–3275PubMed
4.
go back to reference Noda K, Nishiwaki Y, Kawahara M et al (2002) Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small-cell lung cancer. N Engl J Med 346:85–91PubMedCrossRef Noda K, Nishiwaki Y, Kawahara M et al (2002) Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small-cell lung cancer. N Engl J Med 346:85–91PubMedCrossRef
5.
go back to reference Xu Y, Villalona-Calero MA (2002) Irinotecan: mechanisms of tumor resistance and novel strategies for modulating its activity. Ann Oncol 13:1841–1851PubMedCrossRef Xu Y, Villalona-Calero MA (2002) Irinotecan: mechanisms of tumor resistance and novel strategies for modulating its activity. Ann Oncol 13:1841–1851PubMedCrossRef
6.
go back to reference Baldwin AS (2001) Control of oncogenesis and cancer therapy resistance by the transcription factor NF-kappaB. J Clin Invest 107:241–246PubMedCrossRef Baldwin AS (2001) Control of oncogenesis and cancer therapy resistance by the transcription factor NF-kappaB. J Clin Invest 107:241–246PubMedCrossRef
7.
go back to reference Bargou R, Emmerich F, Krappmann D et al (1997) Constitutive activation of NF-kappaB -RelA is required for proliferation and survival of Hodgkin’s disease tumor cells. J Clin Invest 100:2961–2969PubMed Bargou R, Emmerich F, Krappmann D et al (1997) Constitutive activation of NF-kappaB -RelA is required for proliferation and survival of Hodgkin’s disease tumor cells. J Clin Invest 100:2961–2969PubMed
8.
go back to reference Karin M, Cao Y, Greten FR, Li Z (2002) NF-kappaB in cancer: from innocent bystander to major culprit. Nat Rev 2:301–310CrossRef Karin M, Cao Y, Greten FR, Li Z (2002) NF-kappaB in cancer: from innocent bystander to major culprit. Nat Rev 2:301–310CrossRef
9.
go back to reference Mayo MW, Wang C, Cogswell PC et al (1997) Requirement of NF-kappaB activation to suppress p53-independent apoptosis induced by oncogenic Ras. Science 278:1812PubMedCrossRef Mayo MW, Wang C, Cogswell PC et al (1997) Requirement of NF-kappaB activation to suppress p53-independent apoptosis induced by oncogenic Ras. Science 278:1812PubMedCrossRef
10.
go back to reference Beg AA, Baltimore D (1996) An essential role for NF-kappaB in preventing TNF-alpha induced cell death. Science 274:782PubMedCrossRef Beg AA, Baltimore D (1996) An essential role for NF-kappaB in preventing TNF-alpha induced cell death. Science 274:782PubMedCrossRef
11.
go back to reference Wang CY, Mayo MW, Korneluk RG, Goeddel DV, Baldwin AS Jr (1998) NF-kappaB antiapoptosis: induction of TRAF1 and TRAF2 and c-IAP1 and c-IAP2 to suppress caspase-8 activation. Science 281:1680–1683PubMedCrossRef Wang CY, Mayo MW, Korneluk RG, Goeddel DV, Baldwin AS Jr (1998) NF-kappaB antiapoptosis: induction of TRAF1 and TRAF2 and c-IAP1 and c-IAP2 to suppress caspase-8 activation. Science 281:1680–1683PubMedCrossRef
12.
go back to reference Chen C, Edelstein LC, Gelinas C (2000) The Rel/NF-kappaB family directly activates expression of the apoptosis inhibitor Bcl-x(L). Mol Cell Biol 20(8):2687–2695PubMedCrossRef Chen C, Edelstein LC, Gelinas C (2000) The Rel/NF-kappaB family directly activates expression of the apoptosis inhibitor Bcl-x(L). Mol Cell Biol 20(8):2687–2695PubMedCrossRef
13.
go back to reference Cusack JC, Liu R, Baldwin AS (2000) Inducible chemoresistance to 7-Ethyl-10-[4-(1-piperidino)-1-piperidino]-carbonyloxycamptothecin (CPT-11) in colorectal cancer cells and a xenograft model is overcome by inhibition of nuclear factor-kappaB activation. Cancer Res 60:2323–2330PubMed Cusack JC, Liu R, Baldwin AS (2000) Inducible chemoresistance to 7-Ethyl-10-[4-(1-piperidino)-1-piperidino]-carbonyloxycamptothecin (CPT-11) in colorectal cancer cells and a xenograft model is overcome by inhibition of nuclear factor-kappaB activation. Cancer Res 60:2323–2330PubMed
14.
go back to reference Wang C, Cusack JC, Liu R, Baldwin AS (1999) Control of inducible chemoresistance: enhanced anti-tumor therapy through increased apoptosis by inhibition of NF-kappaB. Nat Med 5:412PubMedCrossRef Wang C, Cusack JC, Liu R, Baldwin AS (1999) Control of inducible chemoresistance: enhanced anti-tumor therapy through increased apoptosis by inhibition of NF-kappaB. Nat Med 5:412PubMedCrossRef
15.
go back to reference Moreira AL, Sampaio EP, Zmuidzinas A et al (1993) Thalidomide exerts its inhibitory action on tumor necrosis factor alpha by enhancing mRNA degradation. J Exp Med 177:1675–1680PubMedCrossRef Moreira AL, Sampaio EP, Zmuidzinas A et al (1993) Thalidomide exerts its inhibitory action on tumor necrosis factor alpha by enhancing mRNA degradation. J Exp Med 177:1675–1680PubMedCrossRef
16.
go back to reference D’Amato R, Loughnan MS, Flynn E, Folkman J (1994) Thalidomide is an inhibitor of angiogenesis. Proc Natl Acad Sci USA 91:4082–4085PubMedCrossRef D’Amato R, Loughnan MS, Flynn E, Folkman J (1994) Thalidomide is an inhibitor of angiogenesis. Proc Natl Acad Sci USA 91:4082–4085PubMedCrossRef
17.
go back to reference Kenyon BM, Browne F, D’Amato RJ (1997) Effects of thalidomide and related metabolites in a mouse corneal model of neovascularization. Exp Eye Res 64:971–978PubMedCrossRef Kenyon BM, Browne F, D’Amato RJ (1997) Effects of thalidomide and related metabolites in a mouse corneal model of neovascularization. Exp Eye Res 64:971–978PubMedCrossRef
18.
go back to reference Govindarajan R, Heaton KM, Broadwater R, Zeitlin A, Lang NP, Hauer-Jensen M (2000) Effect of thalidomide on gastrointestinal toxic effects of irinotecan. Lancet 356(9229):566–567PubMedCrossRef Govindarajan R, Heaton KM, Broadwater R, Zeitlin A, Lang NP, Hauer-Jensen M (2000) Effect of thalidomide on gastrointestinal toxic effects of irinotecan. Lancet 356(9229):566–567PubMedCrossRef
19.
go back to reference Keifer JA, Guttridge DC, Ashburner BP, Baldwin AS Jr (2001) Inhibition of NF-kappaB activity by thalidomide through suppression of IκB kinase activity. J Biol Chem 276:22382–22387PubMedCrossRef Keifer JA, Guttridge DC, Ashburner BP, Baldwin AS Jr (2001) Inhibition of NF-kappaB activity by thalidomide through suppression of IκB kinase activity. J Biol Chem 276:22382–22387PubMedCrossRef
20.
go back to reference Yamamoto Y, Yin MJ, Lin KM, Gaynor RB (1999) Sulindac inhibits activation of the NF-kappaB pathway. J Biol Chem 274:27307–27314PubMedCrossRef Yamamoto Y, Yin MJ, Lin KM, Gaynor RB (1999) Sulindac inhibits activation of the NF-kappaB pathway. J Biol Chem 274:27307–27314PubMedCrossRef
21.
go back to reference Yin M, Yamamoto T, Gaynor RB (1998) The anti-inflammatory agents aspirin and salicylate inhibit the activity of IkappaB kinase-beta. Nature 396:77–80PubMedCrossRef Yin M, Yamamoto T, Gaynor RB (1998) The anti-inflammatory agents aspirin and salicylate inhibit the activity of IkappaB kinase-beta. Nature 396:77–80PubMedCrossRef
22.
go back to reference National Cancer Institute Common Toxicity Criteria, version 2.0. 1999 National Cancer Institute Common Toxicity Criteria, version 2.0. 1999
23.
go back to reference Drengler RL, Kuhn J, Schaaf L et al (1999) A phase I and pharmacokinetic trial of oral irinotecan (CPT-11) administered daily for 5 every 3 weeks. J Clin Oncol 17:685–696PubMed Drengler RL, Kuhn J, Schaaf L et al (1999) A phase I and pharmacokinetic trial of oral irinotecan (CPT-11) administered daily for 5 every 3 weeks. J Clin Oncol 17:685–696PubMed
24.
go back to reference Lyon A, Duran G, Raisys VA (1995) Determination of thalidomide by high performance liquid chromatography: methodological strategy for clinical trials. Clin Biochem 28:467–470PubMedCrossRef Lyon A, Duran G, Raisys VA (1995) Determination of thalidomide by high performance liquid chromatography: methodological strategy for clinical trials. Clin Biochem 28:467–470PubMedCrossRef
25.
go back to reference Figg WD, Raje S, Bauer KS et al (1999) Pharmacokinetics of thalidomide in an elderly prostate cancer population. J Pharm Sci 88:121–125PubMedCrossRef Figg WD, Raje S, Bauer KS et al (1999) Pharmacokinetics of thalidomide in an elderly prostate cancer population. J Pharm Sci 88:121–125PubMedCrossRef
26.
go back to reference Liang KY, Zeger SL (1986) Longitudinal data analysis using generalized linear models. Biometrika 73:13–22CrossRef Liang KY, Zeger SL (1986) Longitudinal data analysis using generalized linear models. Biometrika 73:13–22CrossRef
27.
go back to reference Mathijssen RH, van Alphen RJ, Verweij J, Loos WJ, Nooter K, Stoter G, Sparreboom A (2001) Clinical pharmacokinetics and metabolism of irinotecan (CPT-11). Clin Cancer Res 8:2182–2194 Mathijssen RH, van Alphen RJ, Verweij J, Loos WJ, Nooter K, Stoter G, Sparreboom A (2001) Clinical pharmacokinetics and metabolism of irinotecan (CPT-11). Clin Cancer Res 8:2182–2194
28.
go back to reference Teo SK, Colburn WA, Tracewell WG, Kook KA, Stirling DI, Jaworsky MS, Scheffler MA, Thomas SD, Laskin OL (2004) Clinical pharmacokinetics of thalidomide. Clin Pharmacokinet 43(5):311–327PubMedCrossRef Teo SK, Colburn WA, Tracewell WG, Kook KA, Stirling DI, Jaworsky MS, Scheffler MA, Thomas SD, Laskin OL (2004) Clinical pharmacokinetics of thalidomide. Clin Pharmacokinet 43(5):311–327PubMedCrossRef
29.
go back to reference Trifan OC, Durham WF, Salazar VS et al (2002) Cyclooxygenase-2 inhibition with celecoxib enhances antitumor efficacy and reduces diarrhea side effect of CPT-11. Cancer Res 62(20):5778–5784PubMed Trifan OC, Durham WF, Salazar VS et al (2002) Cyclooxygenase-2 inhibition with celecoxib enhances antitumor efficacy and reduces diarrhea side effect of CPT-11. Cancer Res 62(20):5778–5784PubMed
30.
go back to reference Singhal S, Mehta J, Desikan R et al (1999) Antitumor activity of thalidomide in refractory multiple myeloma. N Engl J Med 341(21):1565–1571PubMedCrossRef Singhal S, Mehta J, Desikan R et al (1999) Antitumor activity of thalidomide in refractory multiple myeloma. N Engl J Med 341(21):1565–1571PubMedCrossRef
31.
go back to reference Santos A, Zannetta S, Cresteil T et al (2000) Metabolism of irinotecan (CPT-11) by CYP3A4 and CYP3A5 in humans. Clin Cancer Res 6:2012–2020PubMed Santos A, Zannetta S, Cresteil T et al (2000) Metabolism of irinotecan (CPT-11) by CYP3A4 and CYP3A5 in humans. Clin Cancer Res 6:2012–2020PubMed
32.
go back to reference Gupta E, Wang X, Ramirez J, Ratain MJ (1997) Modulation of glucuronidation of SN-38, the active metabolite of irinotecan, by valproic acid and phenobarbital. Cancer Chemother Pharmacol 39:440–444PubMedCrossRef Gupta E, Wang X, Ramirez J, Ratain MJ (1997) Modulation of glucuronidation of SN-38, the active metabolite of irinotecan, by valproic acid and phenobarbital. Cancer Chemother Pharmacol 39:440–444PubMedCrossRef
33.
go back to reference Allegrini G, Di Paolo A, Falcone S et al (2003) Irinotecan and thalidomide in patients with advanced cancer; evaluation of tolerability and pharmacokinetic interactions. Proc Am Soc Clin Oncol 22:140 (abstr.559) Allegrini G, Di Paolo A, Falcone S et al (2003) Irinotecan and thalidomide in patients with advanced cancer; evaluation of tolerability and pharmacokinetic interactions. Proc Am Soc Clin Oncol 22:140 (abstr.559)
34.
go back to reference Fuchs CS, Moore MR, Harker G, Villa L, Rinaldi D, Hecht JR (2003) Phase III comparison of two irinotecan dosing regimens in second-line therapy of metastatic colorectal cancer. J Clin Oncol 21(5):807–814PubMedCrossRef Fuchs CS, Moore MR, Harker G, Villa L, Rinaldi D, Hecht JR (2003) Phase III comparison of two irinotecan dosing regimens in second-line therapy of metastatic colorectal cancer. J Clin Oncol 21(5):807–814PubMedCrossRef
35.
go back to reference Fujita J, Mestre JR, Zeldis JB, Subbaramaiah K, Dannenberg AJ (2001) Thalidomide and its analogues inhibit lipopolysaccharide-mediated induction of cyclooxygenase-2. Clin Cancer Res 7:3349–3355PubMed Fujita J, Mestre JR, Zeldis JB, Subbaramaiah K, Dannenberg AJ (2001) Thalidomide and its analogues inhibit lipopolysaccharide-mediated induction of cyclooxygenase-2. Clin Cancer Res 7:3349–3355PubMed
36.
go back to reference Argiles JM et al (1992) The role of cytokines in muscle wasting: its relation with cancer cachexia. Med Res Rev 12(6):637–652PubMedCrossRef Argiles JM et al (1992) The role of cytokines in muscle wasting: its relation with cancer cachexia. Med Res Rev 12(6):637–652PubMedCrossRef
Metadata
Title
Thalidomide and celecoxib as potential modulators of irinotecan’s activity in cancer patients
Authors
Miguel Villalona-Calero
Larry Schaaf
Gary Phillips
Gregory Otterson
Kevin Panico
Wenrui Duan
Barbara Kleiber
Manisha Shah
Donn Young
Wan-Hong Wu
John Kuhn
Publication date
01-01-2007
Publisher
Springer-Verlag
Published in
Cancer Chemotherapy and Pharmacology / Issue 1/2007
Print ISSN: 0344-5704
Electronic ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-006-0249-y

Other articles of this Issue 1/2007

Cancer Chemotherapy and Pharmacology 1/2007 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine