About James Ewing, 1866 - 1943

James Ewing (gif)






About Ewing's sarcoma

James Ewing first described the tumour that was to be named after him in the 1920's [1,2]. Ewing's sarcoma is a type of bone cancer found in children and young adults which accounts for 10-15% of all primary malignant bone tumours [3]. The tumour is composed of small round cells, untreated the disease will spread to the lungs and other bones. Any bone can be affected, though the most common sites are the pelvis, thigh, lower leg, upper arm, and rib. Occasionally it can found entirely restricted to soft tissue (Extraosseous Ewing's Sarcoma). The tumour is rare with an estimated incidence of 0.6 per million, it is less common in black and Chinese populations [4]. Ewing distinguished the tumour from osteosarcoma on the grounds that it was responsive to radiotherapy. In the past only around 10% of patients were long term survivors when surgical amputation or radiotherapy were the only treatments, however, drastic improvements in outlook have been achieved with the advent of modern chemotherapy [5].

Ewing first described the tumour as an "endothelioma of bone" believing that it arose from the blood vessels of bone tissue. He later recognised that the histopathologic features were more complex and went on to describe it as a "endothelial myeloma". He described the histopathology as "broad sheets of small polyhedral cells with pale cytoplasm, small hyperchromatic nuclei, well-defined cell borders and complete absence of inter-cellular material". Reports of similar tumours were made in earlier literature (Lucke, 1866; Hildebrand, 1890), but it was the work of Ewing which established that the disease was separate from lymphoma or neuroblastoma [5]. Today it is known that Ewing's sarcoma covers a spectrum ranging from classical Ewing's to those tumours which are positive for neural markers (Peripheral Neuroectodermal Tumours). This range of tumours all share the same genetic features, namely a t(11;22) translocation [6]. Today the origin of Ewing's Tumour still remains unclear.

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James Ewing - Childhood, education, and early career

Born 25th December 1866 in Pittsburgh, Pennsylvania, James was the third of five children of Judge Thomas Ewing and Julia Ewing. At age 14 he suffered from osteomyelitis of the femur which confined him to bed for two years. During this time he was tutored by Henry Gibbons who encouraged his academic skills. Whilst bed bound he entered various competitions and won a microscope, the instrument that was to play a strong role in his future interests in cancer. Ewing attended Amherst College (Massachusetts) taking a B.A. in classics and philosophy, and excelled in his studies. Despite the injury to his leg Ewing was also a keen tennis player, and maintained this interest throughout his life. In 1888 he was accepted into the College of Physicians and Surgeons of New York, and graduated from the Collage three years later [7].

After briefly working at the Western Pennsylvania Hospital Ewing returned to New York and was given a prestigious internship at the Roosevelt Hospital and Sloane Maternity. He spent much of this time in the hospital laboratory and developed a keen interest in pathology. In 1898 Ewing volunteered as contract surgeon to the US army, treating soldiers evacuated from Cuba and Manila. He published several papers on malaria from which many of the soldiers suffered [7, 8].


James Ewing - Cancer Pathologist, 'The Chief'

In 1899 Ewing was appointed as the first Professor of Pathology at Cornell University, a position which he kept for 33 years. His first book Clinical Pathology of blood was published in 1901. In mid 1900 he married Catherine Halsted and his son James was born two years later, sadly his wife and unborn second child died in 1903.

Ewing had a growing interest in tumours, and was instrumental in establishing the P. Huntington Fund for Cancer Research in 1902. Linked with this he became a leading cancer pathologist and was a prolific in writing papers about cancer. Ewing was a co-founder of the American Association for Cancer Research in 1907. This brought him into contact with James Douglas who was a mining engineer but with a medical background. Douglas had an interest in the possible therapeutic potential of radium and went on to found the National Radium Institute in 1913. In the same year Ewing co-founded the American Society for the Control of Cancer (now the American Cancer Society). The friendship between Douglas and Ewing grew, and Ewing became one of the pioneers in using radiotherapy for cancer [7, 8].

After many years work Ewing's successful textbook Neoplastic Diseases was published in 1919. The following year at a meeting of the New York Pathological Society Ewing presented his paper on the malignant bone tumour that was later became known as Ewing's sarcoma. Ewing was one of the first to recognise the potential of radiation as cancer therapy, stating in 1922; 'From the most unexpected source, experimental physics, a new and powerful weapon has been brought into play'. He also had a role in the development of surgical oncology by encouraging surgeons to gain a better understanding of the natural course of cancer. Ewing laid the foundations of what is now known as the Memorial Sloan-Kettering Cancer Centre, building up a strong team of physicians who later distinguished themselves in the various specialities in oncology. His reputation was widespread, his peers referred to him as "The Chief" and "Mr Cancer" [7].


James Ewing on the Cover of Time Magazine 1931

James Ewing died from bladder cancer at the age of 76. He had a large influence in the development of oncology, over a thousand people attended his last rites in 1943.


References

  1. Ewing J. Diffuse endothelioma of bone. Proc N Y Pathol Soc 21, 17-24, 1921 back to text
  2. Ewing J. Further report of endthelial myeloma of bone. Proc N Y Pathol Soc 24, 93-100, 1924. back to text
  3. Souhami R. Incidence and aetiology of malignant primary bone tumours. Bailliere's Clinical Oncology 1, 1-20, 1987.back to text
  4. Jurgens H, Winkler K, Gobel U. Bone Tumours. In Plowman PN, Pinkerton CR (eds) Paediatric Oncology : Clinical practice and controversies. Chapman & Hall Medical. 325-350, 1992.back to text
  5. Craft AW. Chemotherapy of Ewing's sarcoma. Bailliere's Clinical Oncology 1, 205-221, 1987. Use your browsers BACK button to return to the text
  6. Aurias A, Rimbaut C, Buffe D, et al. Chromosomal Translocation in Ewing's sarcoma. M Engl J Med 309, 469-497, 1983.back to text
  7. Zantinga AR, Coppes MJ. James Ewing (1866-1943):'The Chief'. Med Ped Onc 21:505-510, 1993. Use your browsers BACK button to return to the text
  8. James Ewing: cancer man. Huvos AG. Ann Diagn Pathol 1998 Apr;2(2):146-8 Use your browsers BACK button to return to the text



This page by Simon Cotterill
North of England Children's Cancer Research Unit
Department of Child Health
University of Newcastle upon Tyne, UK

First created: 04/06/96
Last modified: 16/03/99