Ten Years Experience with Ewing's Sarcoma

Author:

Gasparini Marco1,Barni Sandro1,Lattuada Angelo1,Musumeci Renato1,Bonadonna Gianni1,Fossati-Bellani Franca1

Affiliation:

1. Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan

Abstract

The series comprises 57 consecutive patients with Ewing's sarcoma admitted to the National Cancer Institute of Milan from 1965 to 1976. In 75 % the disease was confined to one bone, while in 25 % multiple bone and/or visceral lesions were present. Patients with clinically localized tumor treated before 1971 with local therapy, showed a median disease-free survival of 5 months. After 1971, radiotherapy and/or surgery to local tumor was combined with multiple drug chemotherapy (ADM, VCR, CTX) and the projected median disease-free survival increased to 24+ months. In previously untreated patients with advanced tumor adriamycin, used as single drug, achieved an overall response rate of 73 %. This is comparable to that achieved by a new combination including ADM, VCR, CTX, CCNU (75%). This multiple drug regimen is, however, expected to prolong the duration of response.

Publisher

SAGE Publications

Subject

Cancer Research,Oncology,General Medicine

Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Bone and joints;Rosai and Ackerman's Surgical Pathology;2011

2. Joint and Bone Pathology;Modern Surgical Pathology;2009

3. Ewing's Sarcoma Family of Tumors: Current Management;The Oncologist;2006-05-01

4. Ewing Tumour;Paediatric Drugs;2001

5. Sarcoma de Ewing en la infancia: resultados terapéuticos a largo plazo;Revista de Oncología;2000-07

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