Two hundred gastrointestinal stromal tumors: recurrence patterns and prognostic factors for survival.

OBJECTIVE To analyze the outcome of 200 patients with gastrointestinal stromal tumor (GIST) who were treated at a single institution and followed up prospectively. SUMMARY BACKGROUND DATA A GIST is a visceral sarcoma that arises from the gastrointestinal tract. Surgical resection is the mainstay of treatment because adjuvant therapy is unproven. METHODS Two hundred patients with malignant GIST were admitted and treated at Memorial Hospital during the past 16 years. Patient, tumor, and treatment variables were analyzed to identify patterns of tumor recurrence and factors that predict survival. RESULTS Of the 200 patients, 46% had primary disease without metastasis, 47% had metastasis, and 7% had isolated local recurrence. In patients with primary disease who underwent complete resection of gross disease (n = 80), the 5-year actuarial survival rate was 54%, and survival was predicted by tumor size but not microscopic margins of resection. Recurrence of disease after resection was predominantly intraabdominal and involved the original tumor site, peritoneum, and liver. CONCLUSIONS GISTs are uncommon sarcomas. Tumor size predicts disease-specific survival in patients with primary disease who undergo complete gross resection. Tumor recurrence tends to be intraabdominal. Investigational protocols are indicated to reduce the rate of recurrence after resection and to improve the outcome for patients with GIST.

[1]  J M Woodruff,et al.  Retroperitoneal soft-tissue sarcoma: analysis of 500 patients treated and followed at a single institution. , 1998, Annals of surgery.

[2]  L. Kindblom,et al.  Gastrointestinal pacemaker cell tumor (GIPACT): gastrointestinal stromal tumors show phenotypic characteristics of the interstitial cells of Cajal. , 1998, The American journal of pathology.

[3]  S. Hirota,et al.  Gain-of-function mutations of c-kit in human gastrointestinal stromal tumors. , 1998, Science.

[4]  L. Traverso,et al.  Gut stromal tumors and their clinical behavior. , 1997, American journal of surgery.

[5]  M. Silverman,et al.  Gastric Smooth Muscle Tumors: Diagnostic Dilemmas and Factors Affecting Outcome , 1996, World Journal of Surgery.

[6]  J M Woodruff,et al.  Subclassification of gastrointestinal stromal tumors based on evaluation by electron microscopy and immunohistochemistry. , 1996, Ultrastructural pathology.

[7]  M. Miettinen,et al.  Gastrointestinal stromal tumors--value of CD34 antigen in their identification and separation from true leiomyomas and schwannomas. , 1995, The American journal of surgical pathology.

[8]  E. Casper,et al.  Gastrointestinal autonomic nerve tumors. A clinicopathological, immunohistochemical, and ultrastructural study of 12 cases. , 1993, The American journal of surgical pathology.

[9]  D. Coit,et al.  Lymph Node Metastasis From Soft Tissue Sarcoma in Adults Analysis of Data From a Prospective Database of 1772 Sarcoma Patients , 1993, Annals of surgery.

[10]  R. Pollock,et al.  Prognostic implications of patterns of failure for gastrointestinal leiomyosarcomas , 1992, Cancer.

[11]  E. Atkinson,et al.  Prognostic factors influencing survival in gastrointestinal leiomyosarcomas. Implications for surgical management and staging. , 1992, Annals of surgery.

[12]  C. Compton,et al.  Sarcomas of the gastrointestinal tract. Separation into favorable and unfavorable prognostic groups by mitotic count. , 1991, Annals of surgery.

[13]  G. Weiss,et al.  Phase III comparison of doxorubicin and dacarbazine given by bolus versus infusion in patients with soft-tissue sarcomas: a Southwest Oncology Group study. , 1991, Journal of the National Cancer Institute.

[14]  A. Elias,et al.  Response to mesna, doxorubicin, ifosfamide, and dacarbazine in 108 patients with metastatic or unresectable sarcoma and no prior chemotherapy. , 1989, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[15]  L. Cerezo,et al.  Gastrointestinal autonomic nerve tumors. 'Plexosarcomas'. , 1989, Archives of pathology & laboratory medicine.

[16]  J. D. Licht,et al.  Gastrointestinal sarcomas. , 1988, Seminars in oncology.

[17]  G. Parker,et al.  Gastrointestinal sarcomas. Analysis of prognostic factors. , 1987, Annals of surgery.

[18]  H. Evans Smooth muscle tumors of the gastrointestinal tract. A study of 56 cases followed for a minimum of 10 years , 1985, Cancer.

[19]  G. Farr,et al.  Myosarcomas of the small and large intestine: A clinicopathologic study , 1983, Journal of surgical oncology.

[20]  Y. Lee,et al.  Leiomyosarcoma of the gastro-intestinal tract: general pattern of metastasis and recurrence. , 1983, Cancer treatment reviews.

[21]  J. Papo,et al.  Smooth muscle tumors of the alimentary tract , 1983, Journal of surgical oncology.

[22]  Fazio Vw,et al.  Prognostic factors of 28 leiomyosarcomas of the small intestine. , 1982 .

[23]  G. Farr,et al.  Myosarcomas of the stomach: Natural history, prognostic factors and management , 1982, Cancer.

[24]  V. Fazio,et al.  Prognostic factors of 28 leiomyosarcomas of the small intestine. , 1982, Surgery, gynecology & obstetrics.

[25]  J. Raaf,et al.  Gastric leiomyosarcoma: Clinical and pathological review of fifty patients , 1981, Journal of surgical oncology.

[26]  O. Beahrs,et al.  Leiomyosarcoma of the small and large bowel , 1978, Cancer.

[27]  C. Illingworth Progress in Clinical Cancer , 1965 .

[28]  Gray Sw,et al.  SMOOTH MUSCLE TUMORS OF THE ALIMENTARY TRACT. , 1965 .

[29]  R. Buxton Smooth muscle tumors of the gastrointestinal tract. , 1960, The American surgeon.

[30]  M. Dockerty,et al.  Leiomyomas and leiomyosarcomas of the small intestine , 1955, Cancer.