SEER Stat Fact Sheets: Bone and Joint Cancer
Statistics at a GlanceShow More
At a Glance
- Estimated New Cases in 2013 3,010
- Estimated Deaths in 2013 1,440
Lifetime Risk: Lifetime risk is the probability of developing or dying from a disease in the course of one's lifespan. Based on the most recent data, approximately 0.1 percent of men and women will be diagnosed with bone and joint cancer at some point during their lifetime.
Survival StatisticsShow More
How Many People Survive 5 Years Or More after Being Diagnosed with Bone and Joint Cancer?
Relative survival statistics compare the survival of patients diagnosed with cancer with the survival of people in the general population who are the same age, race, and sex and who have not been diagnosed with cancer. Because survival statistics are based on large groups of people, they cannot be used to predict exactly what will happen to an individual patient. No two patients are entirely alike, and treatment and responses to treatment can vary greatly.
Based on data from SEER 18 2003-2009. Gray figures represent those who have died from bone and joint cancer. Green figures represent those who have survived 5 years or more.
Number of New Cases and DeathsShow More
How Common Is This Cancer?
Compared to other cancers, bone and joint cancer is rare.
|Common Types of Cancer||Estimated New
|3.||Lung and Bronchus Cancer||228,190||159,480|
|4.||Colon and Rectum Cancer||142,820||50,830|
|5.||Melanoma of the Skin||76,690||9,480|
|8.||Kidney and Renal Pelvis Cancer||65,150||13,680|
|29.||Bone and Joint Cancer||3,010||1,440|
Bone and joint cancer represents 0.2% of all new cancer cases in the U.S.
In 2013, it is estimated that there will be 3,010 new cases of bone and joint cancer and an estimated 1,440 people will die of this disease.
Who Gets This Cancer?
Osteosarcoma is most common in teenagers. Ewing Sarcoma is most common in teenagers and young adults.
Bone and joint cancer rates are highest in people aged <20 years.
SEER 18 2006-2010, All Races, Both Sexes
- All Races
- Asian /
- Not Shown, <16 casesAmerican Indian /
Alaska NativeNot Shown, <16 cases
SEER 18 2006-2010, Age-Adjusted
Who Dies From This Cancer?
Bone and joint cancer deaths are highest in people aged 75-84 years.
U.S. 2006-2010, All Races, Both Sexes
- All Races
- Asian /
- American Indian /
Alaska NativeNot Shown, <16 cases
U.S. 2006-2010, Age-Adjusted
Trends in RatesShow More
Changes Over Time
Keeping track of the number of new cases, deaths, and survival over time (trends) can help scientists understand whether progress is being made and where additional research is needed to address challenges, such as improving screening or finding better treatments.
Using statistical models for analysis, rates for new bone and joint cancer cases have been rising on average 0.4% each year over the last 10 years. Death rates have been falling on average 0.3% each year over the same period. 5-year survival trends are shown below the figure.
|5-Year Relative Survival||52.2%||48.3%||56.4%||67.6%||74.2%||69.9%||70.9%||70.1%|
SEER 9 Incidence & U.S. Mortality 1975-2010, All Races, Both Sexes
More About This CancerShow More
Cancer and the Bone and Joint
Primary bone cancer is cancer that forms in cells of the bone. Some types of primary bone cancer are osteosarcoma, Ewing sarcoma, malignant fibrous histiocytoma, and chondrosarcoma. Secondary bone cancer is cancer that spreads to the bone from another part of the body (such as the prostate, breast, or lung). Primary bone cancer is far less common than cancer that spreads to the bones.
Bone cancer is a malignant tumor of the bone that destroys normal bone tissue. Not all bone tumors are malignant. In fact, benign (noncancerous) bone tumors are more common than malignant ones.
Common types of primary bone and joint cancer include the following:
Here are some resources for learning more about bone and joint cancer.
- About risk factors for osteosarcoma
- About symptoms and diagnosis of osteosarcoma
- About symptoms and diagnosis of Ewing Sarcoma
- About treatment options for osteosarcoma
- About treatment options for Ewing Sarcoma
- About clinical trials
All statistics in this report are based on statistics from SEER and the Centers for Disease Control's National Center for Health Statistics. Most can be found within:
Howlader N, Noone AM, Krapcho M, Garshell J, Neyman N, Altekruse SF, Kosary CL, Yu M, Ruhl J, Tatalovich Z, Cho H, Mariotto A, Lewis DR, Chen HS, Feuer EJ, Cronin KA (eds). SEER Cancer Statistics Review, 1975-2010, National Cancer Institute. Bethesda, MD, http://seer.cancer.gov/csr/1975_2010/, based on November 2012 SEER data submission, posted to the SEER web site, April 2013.
All material in this report is in the public domain and may be reproduced or copied without permission; citation as to source, however, is appreciated.
SEER Cancer Statistics Factsheets: Bone and Joint Cancer. National Cancer Institute. Bethesda, MD, http://seer.cancer.gov/statfacts/html/bones.html
This factsheet focuses on population statistics that are based on the US population. Because these statistics are based on large groups of people, they cannot be used to predict exactly what will happen to an individual patient. To see tailored statistics, browse the SEER Cancer Statistics Review. To see statistics for a specific state, go to the State Cancer Profiles.
The statistics presented in this factsheet are based on the most recent data available, most of which can be found in the SEER Cancer Statistics Review. In some cases, different year spans may be used. Estimates for the current year are based on past data.
Cancer is a complex topic. There is a wide range of information available. This factsheet does not address causes, symptoms, diagnosis, treatment, follow-up care, or decision making, although it provides links to information in many of these areas.