Posts tagged "mantle cell lymphoma"

Lymphatic Cancer Survival Rate

There are two types of lymphatic cancer viz., Hodgkin lymphatic cancer and Non-Hodgkin lymphatic cancer. The Hodgkin lymphatic cancer is caused due to the abnormal cells called Reed-Sternberg. The non-Hodgkin lymphatic cancer is a cancer caused without the abnormal cell called Reed-Sternberg. The Hodgkin lymphatic cancer has been found to affect mostly young adults . The incidence rate of males getting the Hodgkin lymphoma is higher than that of the females. According to the research, the Hodgkin lymphoma is common among young people of the age less than 20. In the year 2006, there were 1.1 per 100,000 children, who were affected by the Hodgkin lymphoma. The Hodgkin lymphoma is most common in children, as compared to the non-Hodgkin lymphoma.

Lymphatic Cancer Survival and cure rates

More aggressive forms of non-Hodgkin may be fatal, but have a higher likelihood of being cured with chemotherapy. The lower-grade lymphatic cancers have a longer lymphatic survival rate, often 10 or more years, but are often not curable.

Lymphatic Cancer Survival rates by type

Cutaneous anaplastic large cell has the best prognosis, with a 78 percent, five-year survival rate, while peripheral T-cell, anaplastic large T/null cell and angioimmunoblastic lymphoma have a five-year survival rate together of 38 percent to 43 percent. Extranodal NK/T-cell lymphatic cancer and enteropathy-type lymphatic cancer are in the lowest five-year survival rate category, with a prognosis of 22 percent to 24 percent.

Survival rates for non-Hodgkin lymphoma

These factors are important because they allow doctors to plan better than they could if were based only on the type of lymphoma (the pathology report) and staging information.

Each poor prognostic factor is assigned 1 point. People without any poor prognostic factors would have a score of 0, while those with all of the poor prognostic factors would have a score of 5. The index divides people with lymphomas into 4 risk groups:

  • Low (0 or 1 poor prognostic factors)
  • Low intermediate (2 poor prognostic factors)
  • High intermediate (3 poor prognostic factors)
  • High (4 or 5 poor prognostic factors)

In the studies used to develop the index, about 75% of people in the lowest risk group lived longer than 5 years, but only about 30% of people in the highest group lived at least 5 years. These numbers show the difference the index scores can make. But newer treatments mean that survival rates are likely to be higher now.

The IPI allows doctors to plan treatment better than they could just based on the type and stage of the lymphoma. This has become more important as new, better treatments have been found that sometimes have more side effects. The index helps doctors figure out whether these treatments are needed. It also gives patients information about the outlook for their future.

Hodgkins disease survival rate

These are the 5-year survival rates.

Stage I: 90% to 95%

Stage II: 90% to 95%

Stage III: 85% to 90%

Stage IV: Around 80%

Since 1960 the Hodgkins disease survival rate has doubled from 40% to over 86% caused by the improvement of the types of treatments.

The cause of Hodgkins disease is unknown. Many studies are trying to change that.
Decadron Diary: A Family’s Journey Through Hodgkin’s Disease
by: Karen Kondor
publisher: Xlibris, Corp., published: 2011-04-20
ASIN: 1462857450
EAN: 9781462857456
sales rank: 3477244
price: $14.10 (new), $45.80 (used)

Based on a collection of emails, Decadron Diary is a combination memoir and self-help book that details one family’s journey through cancer treatment.  At once serious and humorous, Decadron Diary epitomizes the rollercoaster ride that is the daily experience of  anyone facing cancer, whether that person is the patient, the family member, the physician, the nurse, the psychologist or anyone else who crosses paths with cancer.

Hodgkin Lymphoma
publisher: Lippincott Williams & Wilkins, published: 2007-05-18
ASIN: 078176422X
EAN: 9780781764223
sales rank: 1105253
price: $29.47 (new), $29.46 (used)

The definitive text on Hodgkin lymphoma is now in its thoroughly revised, updated Second Edition. More than 100 recognized authorities from all parts of the world provide comprehensive, current information on every aspect of Hodgkin lymphoma, including etiology, epidemiology, biology, pathology, evaluation, staging, treatment, and follow-up.

This edition describes the increased use of PET scanning in staging and follow-up. Chapters discuss current treatment options—including combination chemotherapy, radiation therapy, novel treatment techniques, and hematopoietic stem cell transplantation—and offer guidelines for treatment selection. Full consideration is given to late effects of therapy and clinical trials for assessing quality of life in patients.

This edition includes complete access to the fully searchable online text of the entire book with all the images.

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Posted by admin - 26/12/2011 at 5:19 am

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What is Mantle Cell Lymphoma?

Mantle cell lymphoma is a subtype of B-cell or B-Lymphocyte lymphoma categorized under Non-Hodgkin’s lymphoma. This type of lymphoma is due to a malignant transformation of the B-cells. These B-cells are part of the immune system and responsible for destroying microorganisms that invade the body. The disease got its name for the malignant B-cells are often found in the mantle zone of the . Under morphological studies, this would present as a non-aggressive type of lymphoma. However, mantle cell lymphoma is an aggressive type of B-cell lymphoma and the malignancy can spread quickly in the body.


Mantle cell lymphoma is a rare-type of Non-Hodgkin’s lymphoma. Comprising about 7% of the patients belonging in this category, it is commonly found in age groups above 60 years old. This type of lymphoma is manifested by swollen, non-tender located in the throat, and can involve other nodes such as the ones located near the collar bone, the armpits, chests, and groin. The malignant cells can also metastasize in the spleen and liver, giving the sensation of a full, distended abdomen. Fatigue in this condition is due to anemia because of spleen and bone marrow involvement may also be observed, as well as unexplained fever and weight loss. Gastric symptoms such as nausea and vomiting can also be observed.


Treatment for mantle cell lymphoma is given depending on the current stage of malignancy and metastasis. Rituximab is used to help the for the malignant cells and destroy them, with the help of Interferon given as an immune system booster. R-CHOP in combination with Rituximab and a steroid is commonly given as a form of chemotherapy that aims in destroying the cancer cells. In Stage I and Stage II phase it is treated with a local radiation therapy with or without the aid of chemotherapeutic agents. To help the body recover, stem cell therapy such as is done as an aggressive form of treatment when the disease is at the later stage.


Research is still being conducted on ways to treat mantle cell lymphoma without suffering from too much side effects. The MCL Consortium is a group of physicians dedicated to battling this disease. Their website has mantle cell lymphoma resources for researchers and patients designed to help people understand this malignancy as well as group together patients and survivors to form a support group.


Need to learn more about Lymphoma? Be sure to check out Lymphoma Symptoms which contains in-depth information on Mantle Cell Lymphoma symptoms, causes, treatment and much more.

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Posted by admin - 24/12/2011 at 4:27 pm

Categories: Lymphatic Cancer   Tags: , , , , , , , , ,

The Prognosis Of Burkitts Lymphoma

Burkitts lymphoma is an exceedingly rare type of cancer. Less than a thousand cases are diagnosed yearly in the United States of America.

However, in some other parts of the world where it is endemic, such as certain parts of central Africa, Burkitt’s lymphoma is very common among children.

Burkitt’s lymphoma is a Non-Hodgkin’s Lymphoma (NHL) cancer that affects B lymphocyte cells. There are 3 distinct varieties of this disease:

-Immunodeficiency-related: This form of the condition occurs most often in HIV patients and similarly immunocompromised individuals such as recent transplant recipients. The condition may signal the onset of AIDS.

-Sporadic: This variant of the disease is found outside of the African continent. It is akin to endemic Burkitt’s lymphoma and is associated with immune system compromise.

-Endemic: This form of the disease is the so-called “African” form and is responsible for the majority of malignant cases in central African children. This form of the disease may affect several areas but most often impacts the jaw, ovaries, breasts, kidneys, facial bone. The Epstein-Barr virus, which is the virus responsible for mononucleosis is closely associated with Burkitt’s.

The symptoms of may include painless, swollen lymph nodes (this is characteristic of lymphomas in general), hardening and/or rapid growth of the lymph nodes. Pain in the abdomen is another possible sign.

This disease can be diagnosed by a variety of modes such as:

-X-ray of the chest
-Blood Count
-Spinal fluid analysis
- and/or bone marrow biopsy
-CT and/or PET scan

Treatment of this disease usually involves intense chemotherapy. The earlier that chemotherapy is started, the better the outlook as this is a particularly aggressive form of cancer. However, some cancers which grow rapidly such as Burkitt’s, respond more quickly to treatment. This can actually harm the patient through a process called tumor lysis syndrome, in which the body is subjected to the byproducts of the breakdown of cancer cells which may cause any of a host of serious complications such as severe electrolyte disruption and renal failure.

Combination chemotherapy may be supplemented with radiotherapy, dietary interventions, nootropics, supplements, exposure to natural sunlight (for vitamin D). Surgery is often indicated for the removal of tumors and a bone marrow transplant may be necessary in the case that the bone marrow is affected.


Burkitt Cancer Fiber
by: Ethel R. Nelson
publisher: TEACH Services, Inc., published: 1998-01-01
ASIN: 1572580933
EAN: 9781572580930
sales rank: 1576028
price: $9.90 (new), $0.33 (used)

The story of Dr. Denis Burkitt, who was renowned in medical circles for discovering a grotesque cancer in children (Burkitt’s lymphoma). His discovery led to the isolating of the first human cancer-causing virus, the Epstein-Barr virus. For more than 20 years Dr. Burkitt tirelessly traversed the world, skillfully lecturing on the potential for preventing disease through improved nutrition, including the dangerous role of a high-fat diet.

21st Century Adult Cancer Sourcebook: Non-Hodgkin Lymphoma (NHL) including Burkitt Lymphoma and Others – Clinical Data for Patients, Families, and Physicians
by: National Cancer Institute
publisher: Progressive Management, published: 2011-10-13
ASIN: B005VQUXZA

Authoritative information and practical advice from the nation’s cancer experts about non-Hodgkin lymphoma (NHL) includes official medical data on signs, symptoms, early detection, diagnostic testing, risk factors and prevention, treatment options, surgery, radiation, drugs, chemotherapy, staging, biology, prognosis, and survival, with a complete glossary of technical medical terms and current references. Burkitt lymphoma is included in this collection.

Starting with the basics, and advancing to detailed patient-oriented and physician-quality information, this comprehensive in-depth compilation gives empowered patients, families, caregivers, nurses, and physicians the knowledge they need to understand the diagnosis and treatment of NHL.

Comprehensive data on clinical trials is included – with information on intervention, sponsor, gender, age group, trial phase, number of enrolled patients, funding source, study type, study design, NCT identification number and other IDs, first received date, start date, completion date, primary completion date, last updated date, last verified date, associated acronym, and outcome measures.

There are many different types of non-Hodgkin lymphoma. These types can be divided into aggressive (fast-growing) and indolent (slow-growing) types, and they can be formed from either B-cells or T-cells. B-cell non-Hodgkin lymphomas include Burkitt lymphoma, chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), diffuse large B-cell lymphoma, follicular lymphoma, immunoblastic large cell lymphoma, precursor B-lymphoblastic lymphoma, and mantle cell lymphoma. T-cell non-Hodgkin lymphomas include mycosis fungoides, anaplastic large cell lymphoma, and precursor T-lymphoblastic lymphoma. Lymphomas that occur after bone marrow or stem cell transplantation are usually B-cell non-Hodgkin lymphomas. Prognosis and treatment depend on the stage and type of disease.

Extensive supplements, with chapters gathered from our Cancer Toolkit series and other reports, cover a broad range of cancer topics useful to cancer patients. This edition includes our exclusive Guide to Leading Medical Websites with updated links to 81 of the best sites for medical information, which let you quickly check for updates from the government and the best commercial portals, news sites, reference/textbook/non-commercial portals, and health organizations. Supplemental coverage includes:

Levels of Evidence for Cancer Treatment Studies
Glossary of Clinical Trial Terms
Clinical Trials Background Information and In-Depth Program
Clinical Trials at NIH
How To Find A Cancer Treatment Trial: A Ten-Step Guide
Taking Part in Cancer Treatment Research Studies
Access to Investigational Drugs
Clinical Trials Conducted by the National Cancer Institute’s Center for Cancer Research at the National Institutes of Health Clinical Center
Taking Time: Support for People with Cancer
Facing Forward – Life After Cancer Treatment
Chemotherapy and You

Burkitt’s lymphoma depends upon the risk-factor of the patient. Caught early (low-risk or low/intermediate risk), combination chemotherapy which has produced survival rates in the 90% range. These figures decline significantly for higher risk cases; ~70% for high/intermediate risk and ~30% for high risk. The total 5 year survival rate for adults with Burkitts lymphoma is about 50 percent.

Jonathyn David writes about Burkitts Lymphoma on his blog, The Symptoms of Lymphoma In Women.

 

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Posted by admin - 24/11/2011 at 5:19 am

Categories: Lymphatic Cancer   Tags: , , , , , , , , ,

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