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Fludarabinc: A new agent with major activity against chronic lymphocytic leukemia. Blood 74: 19. 1989 OBrien S. Kantarjian H. Beran M. Smith T. Koller C. Estcy E. Robertson LE. Lcrncr S. Keating M: Results of fludarabinc and prednisone therapy in 254 patients with chronic lymphocytic Icukcmia with multivariate analysis-derived prognostic model for rcsponsc to treatment. Blood 82: 1695. 1993 Chcson BD. Bennet JM. Rai KR. Grever M. Kay NE. Schiffcr CA. Okcn M M . Keating MJ. Boldt DH. Kcmpin SJ. Foon KA: Guidelines for clinical protocols for chronic lymphocytic leukemia. Recommendations of the National CancerInstitute sponsored working group. J Hcmatol 29: 152. I988 CONFLICT OF INTEREST STATEMENT guez-Roisin has lectured for R. Rodri Almirall Prodesfarma Barcelona, Spain ; , AltanaPharma New Jersey, NJ, USA ; , AstraZeneca Madrid, Spain ; , Boehringer Ingelheim Ingelheim, Germany ; , Pfizer New Jersey, NJ, USA ; and GlaxoSmithKline Hertford, UK ; and has had consultancy arrangements with Almirall Prodesfarma, AltanaPharma, Boehringer Ingelheim, Pfizer, Chiesi Wasserman Parma, Italy ; , GlaxoSmithKline, Laboratoris Dr Esteve SA Barcelona, Spain ; and Novartis Basel, Switzerland ; . He has also received research funding from Almirall Prodesfarma, AstraZeneca, Boehringer Ingelheim, Pfizer, GlaxoSmithKline, Laboratoris Dr Esteve SA and Merck SD Madrid, Spain and idarubicin.

Eventually dissolved and disappeared, leaving the animals tumor-free Fig. 5B; quantified below ; . Similar, although less dramatic, results were observed following the sequential treatment with C. novyi-NT and D10 without MMC ; , but never with D10 and MMC in the absence of C. novyi-NT and rarely with C. novyi-NT alone. The dramatic antineoplastic effects of this combination bacteriolytic therapy COBALT ; were associated with significant toxicity. Approximately 15% of animals with tumors of 350 mm3 in size died within 2472 h of receiving COBALT. This toxicity was clearly related to the size of the tumors, because 45% of animals with larger tumors 700 mm3 ; died. Deaths were not observed after administration of C. novyi-NT spores alone or with chemotherapy alone. Although the reason for the deaths of these animals was not clear, they may have been due to tumor lysis syndrome, a phenomenon previously observed in the clinic when large tumor burdens are rapidly destroyed by antineoplastic agents see Discussion ; . The antineoplastic effects of COBALT were quantified in the experiments shown in Fig. 6. Animals with relatively large s.c. HCT116 tumors starting tumor volume 700 mm3 ; were treated with drugs alone D10 plus MMC ; or C. novyi-NT spores plus the drugs. As can be seen in Fig. 6A, the drugs alone slowed the growth of the tumors, although the tumors continued to grow and the animals had to be killed at 1014 days, when tumor weights exceeded 10% of body weight. The addition of C. novyi-NT spores dramatically enhanced the effects of treatment, with tumors actually shrinking rather than simply slowing. In the experiment shown in Fig. 6A, seven of eight animals had dramatic tumor regressions after only one administration of COBALT, and four of the five animals that survived the therapy were completely cured, with no evidence of tumor regrowth after a further three months time. Significant tumor shrinkage was also seen when mice were given sequential treatment with C. novyi-NT spores plus D10 Fig. 6B ; . However, there was no long-term tumor-free survival and the treatment had to be repeated once every 2 weeks unless the full combination, including MMC, was included. This repetition was associated with additional toxicity, including deaths of 15% of animals with each dose. The full COBALT regimen was therefore preferred on the basis of increased efficacy and reduced overall toxicity. To determine whether COBALT would affect other tumor types, we treated C57BL 6 mice with large syngeneic B16 tumors. In this case, CTX was substituted for MMC, because B16 tumor cells were more sensitive to CTX than to MMC. The drugs alone had some antitumor effects, as expected, although the tumor continued to grow in size and the animals had to be killed within 1 week after beginning therapy Fig. 6C ; . C. novyi-NT spores considerably enhanced these effects: the tumors were observed to shrink rather than simply enlarge at a slower rate Fig. 6C ; . D10 plus C. novyi-NT spores without CTX ; had significant antineoplastic effects on B16 tumors, but the addition of the tumor cytotoxic agent CTX ; further enhanced the efficacy of COBALT Fig. 6C ; . In the B16 tumor model, maintenance COBALT once weekly ; was required to keep the tumors from regrowing, whereas with HCT116 cells a single treatment cured about half the mice. Discussion The results recorded above show that COBALT can result in rapid and dramatic regressions of experimental tumors in mice. Even relatively large tumors could be treated successfully with COBALT, although tumors of the size used in our experiments do not generally respond well to chemotherapeutic agents Figs. 5 and 6 ; . It also clear that many questions remain. For example, the basis for the potent tumor cell killing in the vicinity of the germinating bacteria is not understood. We found that many.

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49 In Aboriginal communities kinship care is much wider than the immediate extended family and can include `distant' relatives such as second or third cousins. People can be kin even though there is no blood relationship Bridge and Freeburn, 2001: 8-9 and ifex. L Gordan JCO 2005; 23: 1096-102 ; . Dosing of RITX in maintenance according to PK levels, targeting 25 ug ml. Treated 312 pts with an OR 59%, CR 27% FL OR 63% CR 36% ; . RITX was given 375 mg m2 wkly x 4 and the maintenance. Median time to first bolus iv single dose was 5 months, to the second next dose 3.5 months and to the third dose 3 months. Single dose maintenance was correct to achieve PK levels. Important data. S Horning et al JCO 2005; 23: 712-9 ; . I-131 Tositumomab BEXXAR ; in pts after progression to RITX. Standard dose 0.65-0.75 Gy TBD according to platelet count, and based on dosimetric calculations. FL OR 86% CR 59% 3y PFS 48%. Very good results. JW Friedberg et al Clin Ca Res 2004; 10: 7789-91 ; . Reviewed radioimmunotherapy: Zevalin Ibritumomab tiutexan Y-90 ; was approved by the FDA in Feb 2002. Zevalin was better than RITX in relapsed pts RITX OR 56% CR 16% and Zevalin OR 80% CR 30% ; . BEXXAR was approved by the FDA in June 2003, demonstrating to be better than Tositumomab alone Bexxar OR 55%, CR 33% and Tositumomab OR 17% CR 8% ; . Problems are related to: Long term toxicity, with appearance of MDS 1.45% yearly similar to ChX; optimal timing preferred for consolidation of first OR 2 y PFS 81%, better than CHOP-RITX Role in aggressive NHL; myeloablative radioimmunotherapy + ASCT AlloSCT; and Retreatment. * OW Press et al SWOG Blood 2003; 102: 1606-12 ; . CHOP and then consolidation with I-131 Tositumomab: OR 90%, CR 67%, 2y PFS 81%. Excellent. N Di Bella Cancer 2005; 103: 978-84 ; . N 24 pts, untreated stage III-IV, low grade, med age 62 yo. Pentostatin 4 mg m2 d 1 & 8 MTZ 10 mg m2 d 1 + RITX 375 mg m2 d 1 & 8 Results were 12 CR + PR. MDR 10 mo. Active and well tolerated. D O'Connor et al JCO 2005; 23: 676-84 ; . Bortezomib Phase II, at 1.5 mg m2 d 1, 4, 8, & 11. N 26 pts. FL: 10 pts, 2 CR + 4PR ; SCL &CLL No responses observed; Marginal zone 2 PR and Mantle cell: 1 CR + NC. Active in certain types, important for Mantle cell lymphoma.
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Cynnig NDM1519 ; : O blaid 57, Ymatal 0, Yn erbyn 0. Motion NDM1519 ; : For 57, Abstain 0, Against 0. I. Options a ; Nasal versus oral tracheal intubation Oral tracheal intubation is the usual method of intubation. Nasal intubation is performed when the surgery is in the oral cavity or on the mandible and when the oral route is difficult or impossible e.g. temporomandibular joint ankylosis, trismus. In situations where visualization of larynx by direct laryngoscopy is poor, blind or fibreoptic intubation through the nasal route can be used. The contraindications to nasal intubation are coagulopathy, severe intranasal pathology, basilar skull fracture and the presence of cerebrospinal fluid CSF ; leak. There are certain practical disadvantages of nasotracheal and iloprost.

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Study of dolastatin 10 NSC 376128 ; in patients with advanced solid tumors. Clin. Cancer Res. 6, 12931301 2000 ; . 34. Doronina, S.O., Toki, B.E., Torgov, M.Y. et al. Development of potent monoclonal antibody auristatin conjugates for cancer therapy. Nat. Biotechnol. 21, 778784 2003 ; . 35. Govindan, S.V., Griffiths, G.L., Hansen, H.J., Horak, I.D., and Goldenberg, D.M. Cancer therapy with radiolabeled and drug toxin-conjugated antibodies. Technol. Cancer. Res. Treat. 4, 375391 2005 ; . A comprehensive review on the current technologies for chemo- and radioimmunotherapy 36. Pagliaro, L.C., Liu, B., Munker, R., Andreeff, M., Freireich, E.J., Scheinberg, D.A., Rosenblum, M.G. Humanized M195 monoclonal antibody conjugated to recombinant gelonin: An anti-CD33 immunotoxin with antileukemic activity. Clin. Cancer Res. 4, 19711976 1998 ; . 37. Fink-Bennett, D.M. and Thomas, K. 90Y-ibritumomab tiuxetan in the treatment of relapsed or refractory B-cell non-Hodgkin's lymphoma. J. Nucl. Med. Technol. 31, 6168 2003 ; . 38. Krasner, C. and Joyce, R.M. Zevalin. 90Yttrium labeled anti-CD20 ibritumomab tiuxetan ; , a new treatment for non-Hodgkin's lymphoma. Curr. Pharm. Biotechnol. 4, 341349 2001 ; . 39. Tempero, M., Leichner, P., Baranowska-Kortylewicz, J., Harrison, K., Augustine, S., Schlom, J., Anderson, J., Wizecarver, J. and Colcher, D. High-dose therapy with 90yttrium-labeled monoclonal antibody CC49: A phase I trial. Clin. Cancer Res. 6, 30953102 2000 ; . 40. Wahl, R.L. Tositumomab and 131I therapy in non-Hodgkin's lymphoma. J. Nucl. Med. 46 Suppl 1, 128S40S 2005 ; . 41. Couturier, O., Supiot, S., Degraef-Mougin, M., Faivre-Chauvet, A., Carlier, T., Chatal, J.F., Davodeau, F., and Cherel, M. Cancer radioimmunotherapy with alpha-emitting nuclides. Eur. J. Nucl. Med. Mol. Imaging 32, 601614 2005 ; . 42. Wu, A, M. and Senter, P.D. Arming antibodies: prospects and challenges for immunoconjugates. Nat. Biotechnol. 23, 11371146 2005 ; . 43. Sharkey, R.M, Karacay, H., Cardillo, T.M., Chang, C.H., McBride, W.J., Rossi, E.A., Horak, I.D., and Goldenberg, D.M. Improving the delivery of radionuclides for imaging and therapy of cancer using pretargeting methods. Clin. Cancer Res. 11 19 Suppl ; , 7109s7121s 2005 ; . This article details strategies for improving payload uptake by tumors using a pretargeting antibody, which has applications in both diagnosis and treatment. 44. Karacay, H., McBride, W.J., Griffiths, G.L., Sharkey, R.M., Barbet, J., Hansen, H.J., and Goldenberg, D.M. Experimental pretargeting studies of cancer with a humanized anti-CEA x murine anti-[In-DTPA] bispecific antibody construct and a 99mTc- 188Re-labeled peptide. Bioconjug. Chem. 11, 842854 2000 ; . 45. Cremonesi, M., Ferrari, M., Chinol, M., Stabin, M.G., Grana, C., Prisco, G., Robertson, C., Tosi, G., and Paganelli, G. Three-step radioimmunotherapy with yttrium-90 biotin: Dosimetry and pharmacokinetics in cancer patients. Eur. J. Nucl. Med. 26, 110120 1999 ; . 46. Liu, G., Mang'era, K., Liu, N., Gupta, S., Rusckowski, M., and Hnatowich, D.J. Tumor pretargeting in mice using 99mTc-labeled morpholino, a DNA analog. J. Nucl. Med. 43, 384391 2002 ; . 47. Kenanova, V., Olafsen, T., Crow, D.M. et al. Tailoring the pharmacokinetics and positron emission tomography imaging properties of anti-carcinoembryonic antigen single-chain Fv-Fc antibody fragments. Cancer Res. 65, 622631 2005 ; . This paper describes generating mutations in the FcRn receptor binding region of therapeutic antibodies to control the clearance kinetics of systemic antibody. 48. Sundaresan, G., Yazaki, P.J., Shively, J.E. et al. 124I-labeled engineered anti-CEA minibodies and diabodies allow high-contrast, antigen-specific small-animal PET imaging of xenografts in athymic mice. J. Nucl. Med. 44, 19621969 2003 ; . 49. Adams, G.P., Schier, R., McCall, A.M., Simmons, H.H., Horak, E.M., Alpaugh, R.K, Marks, J.D., and Weiner, L.M. High affinity restricts the localization and tumor penetration of single-chain fv antibody molecules. Cancer Res. 61, 47504755 2001 ; . 50. Stein, R., Govindan, S.V., Hayes, M., Griffiths, G.L., Hansen, H.J., Horak.

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Intraperitoneal RAIT using a 90Y-labeled MUC1 antibody Antisoma plc, London, U.K. ; in patients with ovarian cancer stage IC-IV and no evidence of disease after debulking and platinum-based chemotherapy, produced significantly prolonged durations of disease-free survival: an 80% survival rate at 5 y, compared with 55% for nonrandomized chemotherapy controls without RAIT P 0.0, 035 ; , and a projected 10 y survival rate of 70% versus 32% for the same controls P 0.003 ; 127 ; . It was reported later that in the 21 patients who achieved complete remission following surgery, chemotherapy, and intraperitoneal RAIT, the median survival was not yet reached at a maximum follow-up of 12 y, with 78% surviving 10 y 128 ; . Earlier work by this group demonstrated that the therapy was more effective and indinavir.

VFT is not medically necessary and not covered as a screening test for the following ophthalmological conditions: Pretreatment for a previous diagnosis of retinal detachment. Previous diagnosis of cataracts unless visual changes have occurred. Diagnosis of cataracts, without glaucoma, prior to cataract extraction. Repeated testing for macular degeneration or central vision loss unless visual changes have occurred. The appropriate diagnosis codes to report for this service are as follows: Syphilis and other venereal diseases 094.81-094.89, 095.8 ; , Malignant neoplasm of other and unspecified sites 190.0-191.9, 192.0, 192.1, ; , Benign neoplasms 224.0-224.9, 225.0-225.3, 227.3, ; , Carcinoma in situ 234.0 ; , Neoplasms of uncertain behavior 237.0, 237.1, 237.6, ; , Neoplasms of unspecified nature 239.7, 239.8 ; , Endocrine, nutritional and metabolic diseases, and immunity disorders 242.00-242.11, 250.50-250.53, 253.0, ; , Neurotic disorders, personality disorders, and other nonpsychotic mental disorders 300.00, 300.11, 310.2 ; , Inflammatory diseases of the central nervous system 320.0-320.9, 321.0, 321.8, ; , Hereditary and degenerative diseases of the central nervous system 331.0, 333.81 ; , Other disorders of the central nervous system 340-342.12, 342.90-342.92, 343.1, ; , Disorders of the eye and adnexa 360.23, 360.29, 361.00-361.9, ; , Cerebrovascular disease 430-437.9 ; , Giant cell arteritis 446.5 ; , Rheumatoid arthritis 714.0 ; , Congenital anomalies 743.20-743.22, 743.51-743.59, 743.61 ; , Headache 784.0 ; , Injury to nerves and spinal cord 950.0951.0 ; , Encounter for long-term current ; use of other medications V58.69 ; , Follow-up examination following completed treatment with high-risk medications, not elsewhere classified V67.51 ; , Observation and evaluation for other specified suspected conditions V71.81-V71.89.

Figs. 5, 6. Absence of metabolic co-operation between BHK and BHK-TK cells. Cells were labelled with 2 tCi ml 3H-TdR for 12 h. Fig. 5 shows confluent cells, and Fig. 6 non-confluent, growing cells, x 800. Fig. 7. BHK-TK~ cells in pure culture, labelled with 3H-TdR for 12 h; post-labelling period, 1 h. x 800 and infliximab.

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Ischemic stroke S. Amaro, V. Obach, A. Cervera, M. Gomez-Choco, X. Urra, A.M. Planas, A. Chamorro, Department of Neurological Sciences, Hospital Clinic and IDIBAPS, Spain and ibritumomab.

Measurement and the benchmarking of performance." `Peer review' is the term most commonly used in this article, although it should be stressed that it represents the more comprehensive set of activities defined by `peer referencing' above. Peer review `nominees' are those individuals in each participant college who were appointed by principals to lead the project. The QIA is yet to evaluate these pilots when their final reports are completed in February 2007 and they are therefore not discussed further here, apart from to comment that each one has taken a very different approach to testing out mechanisms of peer referencing or peer review leading to self-regulation. It is probably fair to say at this stage, that the League for Learning Peer Referencing pilot project seems to have taken the most organic, developmental approach out of all the pilots. Project Aims and Objectives The aims of the L4L Pilot Project were NPRP, 2005 ; : To use the Common Inspection Framework to review and conduct peer verification of the college's selfassessment grades To test the host college's judgement through a mature, professional dialogue for development and quality improvement. Specifically the objectives were NPRP, 2005 ; : To host a two day peer review at each college of the host's college's SelfAssessment Report SAR ; To follow-up each peer review with support from the partners for two to three days of development activities in areas for improvement To share good practice. Evaluation Aims and Objectives The Research Centre, City College Norwich, was approached to conduct an independent review and critical evaluation of the L4L Peer Review framework trialled amongst the first group of colleges, namely Lewisham College, City College Norwich and West Nottinghamshire College. Being funded and intal. PE&RC PhD Education Certificate With the educational activities listed below the PhD candidate has complied with the educational requirements set by the C.T. de Wit Graduate School for Production Ecology and Resource Conservation PE&RC ; which comprises of a minimum total of 32 ECTS 22 weeks of activities ; . Review of Literature 5.6 credits ; - Eco-physiology of sweet cherry. - Alternatives for developing the fruit sector in South Patagonia Argentina ; , with emphasis on sweet cherry production. - Quantitative analysis of agricultural systems and linear programming optimization. Writing of Project Proposal 7 credits ; - Development of a participatory decision support system for the fruit sector in South Patagonia Argentina ; , with emphasis on sweet cherry production. Laboratory Training and Working Visits 6 credits ; - Sweet cherry production systems. Pruning and training systems; INIA, Badajoz, Spain 2003 ; . - Fruit production systems. Integrated pest management; INTA-EEA Alto Valle, General Roca, Argentina 2004 ; . - Writing of regional project INTA ; : Intensive and sustainable development of fruit production systems in South Patagonia; INTA-AER Los Antiguos, Los Antiguos, Argentina 2004 ; . - Writing of national project INTA ; : Influence of biotic and management factors on quality, yield and sustainability of organic and environmentally friendly fruit production systems; INTA Central, Buenos Aires, Argentina 2006 ; . - Writing of international project FP6 program of EU ; : EUropean-Latin American CoInnovation of Agro-ecosystemS EULACIAS INTA-EEA Chubut, Trelew, Argentina 2006 ; . Post-Graduate Courses 5.6 credits ; - Course: Eco-physiology of sweet cherry and orchard management; organizer, translator and participant; INTA-EEA Chubut, Argentina - Washington State University, USA 2006 ; . - International workshops of EULACIAS: a ; Definition of the approach for each module work package ; and common research methodologies along case studies; Universidad de Chapingo, Mexico 2006 ; . b ; Writing of PhD and Post-Doc preliminary proposals; Universidad de la Repblica, Uruguay 2007 ; . c ; Discussion of preliminary research results; Universidad de Chapingo, Mexico 2007 ; . Participant.

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Ask your health care provider any questions you may have about how to use ibritumomab tiuxetan with yttrium-90 and invirase. The OsloFrederikshavn route, which were completed at the start of the year. Investments in new, modern onboard environments on these two vessels amounted to around SEK 80 million. Investments will continue and are an important prerequisite for continued success. We will see investments in vessels and onboard environments, improved guest service and continued development of products and services. The objective is increased customer success, which is one of the most important building blocks for long-term profitability. We measure customer success six times a year for every passenger vessel. The average of the 2006 surveys showed that 42% of guests gave the highest rating for service, loyalty and value. The aim is to increase this figure by three percentage points annually over the next three years. Stena Line's employees are a key success factor and every year the working climate is measured in the survey Stena Voice. Stena Line's average value on the fivedegree scale was 3.95 in 2006, an increase from 3.65 in 2001. The target is to increase the number of departments scoring 4.0 or above. An important challenge for 2006 was, and remains, the high oil price, which partly means new prerequisites for the business. Fuel costs make up a major portion of total costs and a number of measures have been introduced to cut fuel consumption and lessen the effect of the high prices within the framework of the Energy Savings Programme ESP ; . Two examples are the changing of propellers on some vessels and adapting timetables to cut fuel consumption of bunker oil. The HSS ferry Stena Discovery was taken out of service on the Hoek van HollandHarwich route at the beginning of 2007. The reasons are the long crossing and the ferry's high oil consumption, combined with falling passenger volumes and idarubicin!
Sive clinical research and exploration of chemotherapeutic strategies have had little impact on overall survival. However, recent therapeutic developments have opened the door to a new era in the treatment of this disease. New treatment modalities include anti-lymphoma monoclonal antibodies e.g. rituximab ; and radioisotope carriers e.g. Iodine-131 I131 ; tositumomab and Yttrium-90 90Y ; ibritumomab tiuxetan ; and concepts such as myeloablative therapy followed by autologous stem cell transplantation ASCT ; . These have resulted in significantly improved treatment outcome in advanced FL in large multicentre trials. The combination of these novel strategies in multimodal approaches justifies optimism about the improving long-term outcome of patients suffering from FL, possibly challenging the standard view that the advanced disease is incurable and iressa.

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Robin McCune, RN CPN CPON Biotherapy is one of the most recent developments in cancer treatment and is now recognized as the fourth modality for treating cancer. Biotherapy is an innovative therapy that uses the body's immune system to target cancer cells. Biotherapy combats cancer by augmenting, modulating, or restoring the host's immune responses, directly interfering with tumor activity, or by affecting the tumor's ability to replicate. The term immunotherapy is often used interchangeably with biotherapy. Monoclonal antibodies and cytokines are examples of biotherapeutic agents. Cancer cells have very unique characteristics that allow them to successfully proliferate. These cells are self-sufficient; they do not need exogenous growth factors. Cancer cells are able to avoid apoptosis, or programmed cell death, by inactivating the telomerase chromosome. A third cell characteristic is the ability to form new blood vessels to sustain growth. Last, unlike normal cells, malignant cells have the ability to replicate continuously and are able to spread to other sites in the body. As researchers have discovered more intricate details of the human immune system and the characteristics of malignant cells, technologic advances have allowed the development of additional agents that mimic the body's immune defense mechanisms and target malignant cells. Many of these are biotherapy agents. Cancer cells have specific and unique antigens on the cell surface. Monoclonal antibodies MABs ; seek out these antigens and bind to the cancer cells; this is known as targeted therapy. Once attached to the cancer cells, MABs can alter the activity of the targeted antigen and signal to the immune cells to destroy the cancer cells. A benefit of targeted therapy is that normal cells are spared from the side effects commonly seen with traditional treatments for cancer. However, biotherapeutic agents are not without side effects of their own. Table 1 summarizes the side effects and nursing considerations when administering biotherapeutic agents. Researchers have found that combining an MAB with chemotherapy or radioactive substances increases the efficacy of the MAB. Recently, the Food and Drug Administration FDA ; has approved two radiopharmaceuticals for the treatment of cancer. Radiopharmaceuticals are MABs that have a radioactive source attached to them for cancer-killing effect Kaplow, 2005 ; . Ibritumomab tiuxetan Zevalin ; , a radiopharmaceutical, has been approved by the FDA to treat relapsed or refractory lowgrade follicular or transformed B-cell non-Hodgkin's lymphoma. Zevalin and rituximab Rituxan ; , both MABs, work in combination to target the CD20 protein on B-cells, and then a high dose of radiation is delivered to the tumor. Increased toxicities and severe infusion reactions have been reported with this regimen. Another radiopharmaceutical combination that was recently approved is the combination of tositumomab and iodine 131 tositumomab Bexxar ; . This combination was approved for treating patients with CD20 positive follicular non-Hodgkin's lymphoma that cannot be treated with rituximab and have relapsed after receiving chemotherapy. Tositumomab.

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