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Essay: Leukemia

Leukemia research paper kettering.. critical analysis creative writing

❶Results from a large phase III clinical trial suggest that a highly intensive preparatory regimen should be used for younger patients with acute myeloid leukemia or myelodysplastic syndromes preparing to undergo an allogeneic stem cell transplant.

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Leukemia Research

Man-made versions, called monoclonal antibodies , can be designed to attack a specific target, such as a protein on the surface of leukemia cells. An example is blinatumomab Blincyto , a special kind of monoclonal antibody that can attach to 2 different proteins at the same time. One part of blinatumomab attaches to a protein found on B cells the cells that become leukemia cells in most cases of ALL.

Another part of the antibody attaches to a protein on immune cells called T cells. By binding to both of these proteins, this drug brings the leukemia cells and immune cells together, which is thought to cause the immune system to attack the cancer cells. Early results with this drug against B-cell ALL have been promising, although so far it has been studied more in adults than in children.

The American Cancer Society medical and editorial content team Our team is made up of doctors and master's-prepared nurses with deep knowledge of cancer care as well as journalists, editors, and translators with extensive experience in medical writing.

See all references for Leukemia in Children. April 17, Last Revised: For reprint requests, please see our Content Usage Policy. Leukemia in Children About Childhood Leukemia. The work is devoted to the burning and important topic of childhood with leukemia. It tells about the disease, its symptoms, and causes, current methods of treatment. It also observes the side effects and long-term prospects for children after the treatment.

The work researches the physical and mental condition of children while treatment. It gives the information about the statistics of positive treatment. The work explains the spiritual experiences and the stages of emotional development that children with leukemia pass while treatment.

Life expectancy during years after diagnosis was able to get very rare. The discovery of new drugs from the class of cytostatics and a clear focus on chemotherapy, as the leading method of treatment gave the opportunity to cure nearly half of all patients. In the past two decades due to intensification of therapy — the introduction of high doses of chemotherapeutic agents, transplantation of stem cells in bone marrow and peripheral blood, to 70 percent of sick children are cured in the developed world.

The findings could help guide the development of treatments tailored specifically for childhood AML. On December 22, FDA approved an update to the label of nilotinib Tasignia that states that some patients with CML who are taking nilotinib and whose cancer has been in remission for an extended period can safely stop taking it.

Interim results from an ongoing clinical trial show that patients with relapsed or refractory chronic lymphocytic leukemia treated with rituximab plus venetoclax have longer progression-free survival compared with patients treated with chemotherapy.

In a unique clinical trial, a group of oncologists with experience treating acute promyelocytic leukemia are making themselves available around the clock to help clinicians at hospitals across the country treat their APL patients. The approval covers patients with B-cell ALL whose disease has relapsed or is refractory to standard chemotherapy.

FDA changed its accelerated approval of blinatumomab Blincyto for some patients with acute lymphoblastic leukemia to a full approval and expanded the approved indications for its use.

The FDA has approved a new formulation of rituximab, Rituxan Hycela, that reduces treatment administration time for patients with several types of blood cancer. The approval also covers several rare conditions. Results from a large phase III clinical trial suggest that a highly intensive preparatory regimen should be used for younger patients with acute myeloid leukemia or myelodysplastic syndromes preparing to undergo an allogeneic stem cell transplant.

Patients with previously treated acute lymphoblastic leukemia who received blinatumomab, which encourages the immune system to kill cancer cells, lived longer and experienced fewer side effects than patients given standard chemotherapy.

Researchers have created a long-sought-after mouse model for an aggressive form of acute lymphoblastic leukemia that occurs commonly in infants and that the researchers believe can accelerate the development of new therapies for the disease. Researchers have developed an immunotherapy approach that uses immune cells whose natural cancer killing abilities have been enhanced in the lab.

In a small clinical trial, the treatment led to remissions in about half of patients with acute myeloid leukemia. Research from TARGET, an NCI-funded program supporting genomic analyses of childhood cancers, has led to the launch of several clinical trials of targeted therapies to treat children with acute lymphoblastic leukemia. The FDA has approved venetoclax for patients with chronic lymphocytic leukemia whose tumors have a specific genetic alteration.

Reports from early-stage trials of two new oral drugs provide hope for patients with high-risk chronic lymphocytic leukemia. The persistence of genetic mutations in some patients with acute myeloid leukemia may allow physicians to better classify their risk of recurrence. Children and young adults age 1 to age 30 with chemotherapy-resistant B-cell acute lymphoblastic leukemia ALL experienced high remission rates following treatment with an experimental immunotherapy.

Results demonstrated that the immunotherapy treatment had anti-leukemia effects in patients and that the treatment was feasible and safe. Patients who received ibrutinib also lived longer and were more likely to show a clinical response to treatment than those who received ofatumumab. Overall survival was also improved in patients who received idelalisib plus rituximab. Patients who received idelalisib and rituximab were also more likely to live 12 months after beginning treatment and to have their cancer regress compared with patients who received a placebo plus rituximab.

Investigators for The Cancer Genome Atlas TCGA Research Network have detailed and broadly classified the genomic alterations that frequently underlie the development of acute myeloid leukemia AML , a deadly cancer of the blood and bone marrow.

Their work paints a picture of a cancer marked by relatively few mutations compared to other types of cancer occurring in adults.


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Research Paper on Leukemia - Over one million Americans in the United States are living with or have been diagnosed with leukemia. That’s a big amount of people.

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Leukemia Research an international journal which brings comprehensive and current information to all health care professionals involved in basic and applied clinical research in hematological malignancies. The editors encourage the submission of articles relevant to hematological malignancies. In conclusion, Leukemia can be fatal, but with early diagnosis, proper treatments, and a lot of luck, it can be put into remission. With treatment options improving constantly, there may one day be a sure cure.

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Type of paper: Research Papers Subject: Medicine Words: Leukaemia in medical terms is a cancer of blood marrow, caused by the abnormal increase in blood cells in a particular organism. In fact, leukaemia has various forms and is a group of diseases that are comprised in the group of haematological neoplasm. This can lead to serious problems such as anemia, bleeding, and infections. Leukemia cells can also spread to the lymph nodes or other organs and cause swelling or pain. This paper examines how leukemia is diagnosed, the main types of treatment of leukemia and possible causes of leukemia (Bhojwani, ).