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In the majority of industrialised countries, fruits and vegetables provide an estimated 2-3 mg day of pro-vitamin A carotenoids, of which -carotene is the principal component Granado et al, 1996 ; . An approximate -carotene intake of 1.8 mg day in a randomly selected population of women in the USA has been reported Chug-Ahuja et al, 1993 ; , the main dietary sources being carrots, orange juice, oranges, tomatoes and dark green leafy vegetables. The average intake in the German National Food Consumption Survey was 1.81 mg day Pelz et al, 1998 ; , mainly from carrots. An average -carotene intake of 1.7-2.1 mg day has been reported in Finland Heinonen, 1991 ; , and of 3.0 mg day in The Netherlands Goldbohm et al, 1998 ; . Levels of fruit and vegetable consumption, however, vary greatly between individuals and -carotene intake may be much higher than average in people who regularly consume substantial amounts of foods such as carrots Gregory et al, 1990; Scott et al, 1996 ; . Some authors have reported that -carotene intake varies according to seasonal factors, perhaps due to the differing availability of specific fruits and vegetables, or because of factors such as light and heat that may affect the carotenoid content of foods Olmedilla et al, 1994; Rautalahti et al, 1993; Takagi et al, 1990 ; . The SCF has not recommended the consumption of -carotene and carotenoids in general, beyond what is needed to supply vitamin A SCF, 1993.
Patient home professional home newsletters feedback survey main menu home conference coverage professional education cme cancer news disease centers physician resources about us oncology stocks - 71 - 9% ; 0 0% ; 0 0% ; - 48% ; cancer news : article ellence and cmf superior to cmf alone for adjuvant therapy of early breast cancer british researchers associated with the national epirubicin adjuvant trial neat ; have reported that ellence epirubicin ; plus cmf cyclphosphamide, methotrexate and fluorouracil ; is superior to cmf alone for adjuvant therapy of women with early breast cancer.
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Schutt P, Ebeling P, Buttkereit U, et al. Eur J Haematol, 2005 January; 74 1 ; : 40-6. : highwire anford cgi medline pmid; 15613105 The authors evaluated the efficacy and side effects of thalidomide 400 mg d ; in combination with vincristine, epirubicin and oral dexamethasone VED ; . Thirty-one patients were enrolled, 12 patients were exclusively treated with thalidomide in combination with VED and 19 patients received high-dose melphalan, for consolidation. The results showed CR in 19%, PR in 61%, stable disease in 16%, and progressive disease in one patient 3.2.
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Tumor activity. Investigational New Drugs, 13, 181186. Lissoni, P., Barni, S., Ardizzoia, A., Tancini, G., Conti, A., & Maestroni, G. 1994a ; . A randomized study with the pineal hormone melatonin versus supportive care alone in patients with brain metastases due to solid neoplasms. Cancer, 73, 699701. Lissoni, P., Barni, S., Brivio, F., Rossini, F., Fumagalli, L., Ardizzoia, A., et al. 1995 ; . A biological study on the efficacy of low-dose subcutaneous interleukin-2 plus melatonin in the treatment of cancer-related thrombocytopenia. Oncology, 52, 360362. Lissoni, P., Barni, S., Cattaneo, G., Tancini, G., Esposti, G., Esposti, D., & Fraschini, F. 1991 ; . Clinical results with the pineal hormone melatonin in advanced cancer resistant to standard antitumor therapies. Oncology, 48, 448450. Lissoni, P., Barni, S., Cazzaniga, M., Ardizzoni, A., Rovelli, F., Brivio, F., et al. 1994b ; . Efficacy of the concomitant administration of the pineal hormone melatonin in cancer immunotherapy with low-dose IL-2 in patients with advanced solid tumors who had progressed on IL-2 alone. Oncology, 51, 344347. Lissoni, P., Barni, S., Tancini, G., Ardizzoia, A., Ricci, G., Aldeghi, R., et al. 1994c ; . A randomized study with subcutaneous low-dose interleukin 2 alone vs interleukin 2 plus the pineal neurohormone melatonin in advanced solid neoplasma other than renal cancer and melanoma. British Journal of Cancer, 69, 196199. Lissoni, P., Pittalis, S., Ardizzoia, A., Brivio, F., Barni, S., Tancini, G., et al. 1996a ; . Prevention of cytokine-induced hypotension in cancer patients by the pineal hormone melatonin. Supportve Care in Cancer, 4, 313316. Lissoni, P., Tancini, G., Barni, S., Paolorossi, F., Rossini, F., Maffe, P., et al. 1996b ; . The pineal hormone melatonin in hematology and its potential efficacy in the treatment of thrombocytopenia. Recenti Progressi in Medicina, 87, 582585. Lissoni, P., Tancini, G., Paolorossi, F., Mandala, M., Ardizzoia, A., Malugani, F., et al. 1999 ; . Chemoneuroendocrine therapy of metastatic breast cancer with persistent thrombocytopenia with weekly low-dose epirubicin plus melatonin: A phase II study. Journal of Pineal Research, 26, 16973. Maehara, Y., Inutsuka, S., Takeuchi, H., Baba, H., Kusumoto, H., & Sugimachi, K. 1993 ; . Postoperative PSK and OK-432 immunochemotherapy for patients with gastric cancer. Cancer Chemotherapy Pharmacology, 33, 171 175. Martindale, W. 1999 ; . Martindale the extra pharmacopoeia. London: Royal Pharmaceutical Society, Pharmaceutical Press. McDougal, A., Sethi Gupta, M., Ramamoorthy, K., Sun, G., & Safe, S.H. 2000 ; . Inhibition of carcinogen-induced rat mammary tumor growth and other estrogen-dependent responses by symmetrical dihalo-substituted analogs of diindolylmethane. Cancer Letter, 151, 168179. McKevoy, G.K. Ed. ; . 1998 ; . AHFS drug information. Bethesda, MD: American Society of Health-System Pharmacists. Mechelany, C., Schlumberger, M., Challeton, C., Comoy, E., & Parmentier, C. 1991 ; . TRIAC 3, 5, 3'-triiodothyroacetic acid ; has parallel effects at the pituritary and peripheral tissue levels in thyroid cancer patients treated with L-thyroxine. Clinical Endocrinology, 35, 123128. Meydani, S.N., & Dinarello, C.A. 1993 ; . Influence of dietary fatty acids on cytokine production and its clinical implications. Nutrition in Clinical Practice, 8, 6572. Micromedex Healthcare Series. 2003 ; . Micromedex Healthcare Series. Englewood, CO: Micromedex Inc. Miller, A.L. 1999 ; . Therapeutic considerations of L-glutamine: A review of the literature. Alternative Medicine Review, 4, 239248. Mizutani, Y., & Yoshida, O. 1991 ; . Activation by the protein-bound polysaccharide PSK krestin ; of cytotoxic lymphocytes that act on fresh autologous tumor cells and T24 human urinary bladder transitional carcinoma cell line in patients with urinary bladder cancer. Journal of Urology, 145, 10821087. Montbriand, M.J. 1993 ; . Freedom of choice: An issue concerning alternate therapies chosen by cancer patients. Oncology Nursing Forum, 20, 1195 1201. Montbriand, M.J. 1994a ; . Decision heuristics of patients with cancer: Alternate and biomedical choices. Unpublished doctoral dissertation, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada and epoprostenol.
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Study 1 ; and raises the issue of benefits compared with costs of physical activity. He has raised similar issues regarding our previous reports 2, 3 ; . Despite his intricate calculations, Dr. Kessler misses the point of our study. First, although it may take several years of activity to prevent a single cardiovascular event among the least active group as a whole, for each individual woman, only 30 minutes to 1 hour of moderate to vigorous exercise per day is needed. Second, Dr. Kessler considers only the lowest and highest risk groups and ignores women in the middle categories. As we showed, the inverse association between physical activity and risk for cardiovascular disease is approximately linear, and women in the middle categories 1 hour of exercise per week ; also benefit substantially from exercise. Third, exercise has numerous other benefits, such as reducing blood pressure, increasing levels of high-density lipoprotein cholesterol, maintaining healthy weight, preventing osteoporosis, reducing risk for some types of cancer, and improving quality of life 4 ; . Exercise is one of the most cost-effective ways to reduce morbidity and mortality. Unfortunately, most of the U.S. population is sedentary.
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Economics and culture, a contribution measured, for instance, by the unprecedented number of Jewish Nobel Prize laureates. The Jewish theatre must continue to be part of this tradition of continuously demanding progress. It must therefore be a laboratory for radical thinking. It must be a laboratory for subversive oppositionist ideas. It must cast doubt upon every establishment, every regime, and every idea. It must protest against every injustice and support all those whose rights are infringed. It must be both farseeing and deep-seeing. Without bias. Without shame. Out of an aspiration to decode human nature, out of an aspiration to bring about a true Tikun Olam. And indeed, not by chance this conference is entitled "Tikun Olam" A World Reform - and not "Tikun Ha'am Hayehudi" which means the reform of the Jewish People. This choice expresses a trend embedded in our collective subconscious as Jews, and reflects our desire to be part of a global stream that encompasses the whole world as our field of activity. As I have contended earlier, the global stream will only be of value side by side with the particularist stream. For two thousand years our particular culture was mainly religious, and only at the end of the 19th century, with the inception of Zionism, was it joined by clear nationalist elements. It was in the wake of the Holocaust and the establishment of the State of Israel that these nationalist elements became the main thrust of our particular culture. It is still unclear whether, as many predict, the globalization process will actually weaken nationalism in the world. If it does, then the centrality of the State of Israel in Jewish culture will become weakened, and Jewish culture will have to define a particular identity for itself that is not based on nationalism, and apparently not on religion either. On what, then, will our future particular identity focus? I hope that the focus will be on the same aspiration towards progress, depth, and universal justice on the same "Tikun Olam", whose importance was sensed by the organizers of this conference, and who chose it as the title of their vision and erbitux.
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Drug names that are capitalized are brand names. The drugs that are not capitalized are generic, with the exception of APAP propoxphene, which is a generic. The following are abbreviations used in the tables and the explanations of each: mg mg ac mcg meq IU IU ac sol inj tab tab cr tab er cap cap cr ophth sol milligram, which is 1 000th of a gram milligrams per actuation spray ; microgram, which is 1 1-millionth of a gram milliequivalent, an alternate form of measurement International Unit, a measurement of biological activity International Units per actuation spray ; solution injection tablet controlled release tablet extended release tablet capsule controlled release capsule ophthalmologic solution.
Et al. Assessing the quality of reports of randomized clinical trials: is blinding necessary? Control Clin Trials. 1996; 17: 1-12. [PMID: 8721797] 22. Sonneveld P, de Ridder M, van der Lelie H, Nieuwenhuis K, Schouten H, Mulder A, et al. Comparison of doxorubicin and mitoxantrone in the treatment of elderly patients with advanced diffuse non-Hodgkin's lymphoma using CHOP versus CNOP chemotherapy. J Clin Oncol. 1995; 13: 2530-9. [PMID: 7595704] 23. Tirelli U, Errante D, Van Glabbeke M, Teodorovic I, Kluin-Nelemans JC, Thomas J, et al. CHOP is the standard regimen in patients 70 years of age with intermediate-grade and high-grade non-Hodgkin's lymphoma: results of a randomized study of the European Organization for Research and Treatment of Cancer Lymphoma Cooperative Study Group. J Clin Oncol. 1998; 16: 27-34. [PMID: 9440719] 24. Cooper IA, Wolf MM, Robertson TI, Fox RM, Matthews JP, Stone JM, et al. Randomized comparison of MACOP-B with CHOP in patients with intermediate-grade non-Hodgkin's lymphoma. The Australian and New Zealand Lymphoma Group. J Clin Oncol. 1994; 12: 769-78. [PMID: 7512131] 25. Aviles A, Nambo MJ, Talavera A, Garcia EL, Huerta-Guzman J, Diaz Maqueo JC. Epirubicin CEOP-Bleo ; versus idaurubicin CIOP-Bleo ; in the treatment of elderly patients with aggressive non-Hodgkin's lymphoma: dose escalation studies. Anticancer Drugs. 1997; 8: 937-42. [PMID: 9436636] 26. Aoki S, Tsukada N, Nomoto N, Maruyama S, Takahashi M, Moriyama Y, et al. Effect of pirarubicin for elderly patients with malignant lymphoma. J Exp Clin Cancer Res. 1998; 17: 465-70. [PMID: 10089069] 27. De Lena M, Maiello E, Lorusso V, Brandi M, Calabrese P, Romito S, et al. Comparison of CHOP-B vs CEOP-B in `poor prognosis' non-Hodgkin's lymphomas. A randomized trial. Med Oncol Tumor Pharmacother. 1989; 6: 163-9. [PMID: 2473364] 28. Meyer RM, Browman GP, Samosh ML, Benger AM, Bryant-Lukosius D, Wilson WE, et al. Randomized phase II comparison of standard CHOP with weekly CHOP in elderly patients with non-Hodgkin's lymphoma. J Clin Oncol. 1995; 13: 2386-93. [PMID: 7666098] 29. Bastion Y, Blay JY, Divine M, Brice P, Bordessoule D, Sebban C, et al. Elderly patients with aggressive non-Hodgkin's lymphoma: disease presentation, response to treatment, and survival--a Groupe d'Etude des Lymphomes de l'Adulte study on 453 patients older than 69 years. J Clin Oncol. 1997; 15: 294553. [PMID: 9256139] 30. Gordon LI, Harrington D, Andersen J, Colgan J, Glick J, Neiman R, et al. Comparison of a second-generation combination chemotherapeutic regimen mBACOD ; with a standard regimen CHOP ; for advanced diffuse non-Hodgkin's lymphoma. N Engl J Med. 1992; 327: 1342-9. [PMID: 1383819] 31. Silingardi V, Federico M, Cavanna L, Avanzini P, Gobbi PG, Lombardo M, et al. ProMECE-CytaBOM vs MACOP-B in advanced aggressive nonHodgkin's lymphoma: long term results of a multicenter study of the Italian Lymphoma Study Group GISL ; . Leuk Lymphoma. 1995; 17: 313-20. [PMID: 8580801] 32. Jelic S, Milanovic N, Tomasevic Z, Matkovic S, Gavrilovic D. Comparison of two non-anthracycline-containing regimens for elderly patients with diffuse large-cell non Hodgkin's lymphomapossible pitfalls in results reporting and interpretation. Neoplasma. 1999; 46: 394-9. [PMID: 10732870] 33. Montserrat E, Garcia-Conde J, Vinolas N, Lopez-Guillermo A, Hernandez ~ Nieto L, Zubizarreta A, et al. CHOP vs. ProMACE-CytaBOM in the treatment of aggressive non-Hodgkin's lymphomas: long-term results of a multicenter randomized trial. PETHEMA: Spanish Cooperative Group for the Study of Hematological Malignancies Treatment, Spanish Society of Hematology ; . Eur J Haematol. 1996; 57: 377-83. [PMID: 9003479] 34. Haioun C, Lepage E, Gisselbrecht C, Bastion Y, Coiffier B, Brice P, et al. Benefit of autologous bone marrow transplantation over sequential chemotherapy in poor-risk aggressive non-Hodgkin's lymphoma: updated results of the prospective study LNH87-2. Groupe d'Etude des Lymphomes de l'Adulte. J Clin Oncol and ergotamine.
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Prior review takes place on only around 10, 000 of them World Bank, 2005a ; . For contracts not subject to prior review the Bank employs ex post reviews, a process similar to prior review but only undertaken for a small, random sample of project contracts World Bank, 2001, pp.176-202 ; . 14 The interviews were held on the assurance of confidentiality. The interviewees had all managed Bank procurement contracts for firms won under international competitive bidding, mostly in the health and education sectors, and mostly under International Development Association IDA ; credits in subSaharan Africa. Between them they have over 30 years experience on approximately 90 contracts, under 70 projects in over 20 countries. The combined value of those contracts is approximately US million, and the combined value of the projects is approximately US.04 billion. The author also had access to all files relating to those contracts, including the bidding documents, bids submitted, contracts and communications between all parties and epirubicin.
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ArQule, a US-based biotechnology company engaged in the research and development of next-generation, small molecule cancer drugs, has granted Japanese company Kyowa Hakko Kogyo an exclusive licence to develop and commercialise ARQ 197 in Japan and parts of Asia Deal no. 27099 ; . Under the terms of the agreement, ArQule will receive US3 M in upfront and potential development milestone payments, including a US M cash upfront licensing fee. In addition, the agreement includes undisclosed sales milestone payments and double-digit royalties on net sales of ARQ 197. Kyowa will be responsible for clinical development costs and commercialisation of the compound in Japan, China, Hong Kong, South Korea and Taiwan. ARQ 197 is the lead product from ArQule's Cancer Survival Protein modulation programme. This small molecule mediates its effects by inhibiting the activity of c-Met, a receptor tyrosine kinase that plays multiple key roles in human cancer, including cancer cell growth, survival, angiogenesis, invasion and metastasis. Preclinical findings have demonstrated that ARQ 197 inhibits c-Met in a wide range of human tumour cell lines, and possesses antitumour activity against several types of xenografted human tumours in mice. Phase I data demonstrated clinical tolerability, pharmacokinetics and signs of antitumour activity in cancer patients with a broad range of metastatic solid tumour types who had failed earlier treatment regimens. ArQule's portfolio consists of two other clinical stage compounds ARQ 501 and ARQ 171. These E2F1 pathway activators result from an alliance with F. Hoffmann-La Roche, entered into in April 2004 Deal no. 16176 ; . Under the terms of this agreement, Roche obtained an option to license drugs resulting from ArQule's E2F programme in the field of cancer therapy. ARQ 197 adds to Kyowa's strong portfolio of anticancer drugs, which include mitomycin, 5-fluorouracil 5-FU ; , Leunase Escherischia coli L-asparaginase ; , Adriacin doxorubicin ; , Hysron H-200 medroxyprogesterone acetate ; , dacarbazine, Farmorubicin epirubicin ; , Platosin cisplatin ; and Navelbine vinorelbine ; . This oncology franchise positions the company strongly in Asian markets, and will allow it to develop and commercialise ARQ 197 effectively.
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