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Post-imatinib surgery in advanced/metastatic GIST: is it worthwhile in all patients?
Mussi, C; Ronellenfitsch, U; Jakob, J; Tamborini, E; Reichardt, P; Casali, P G; Fiore, M; Hohenberger, P; Gronchi, A.
Affiliation
  • Mussi C; Melanoma and Sarcoma Unit, Department of Surgery, Istituto Nazionale Tumori, Milan, Italy.
  • Ronellenfitsch U; Division of Surgical Oncology and Thoracic Surgery, Department of Surgery, University Hospital Mannheim, University of Heidelberg, Germany.
  • Jakob J; Division of Surgical Oncology and Thoracic Surgery, Department of Surgery, University Hospital Mannheim, University of Heidelberg, Germany.
  • Tamborini E; Experimental Molecular Pathology, Department of Pathology, Istituto Nazionale Tumori, Milan, Italy.
  • Reichardt P; Department of Hematology, Oncology and Palliative Care, HELIOS Medical Center, Bad Saarow, Germany.
  • Casali PG; Department of Cancer Medicine, Istituto Nazionale Tumori, Milan, Italy.
  • Fiore M; Melanoma and Sarcoma Unit, Department of Surgery, Istituto Nazionale Tumori, Milan, Italy.
  • Hohenberger P; Division of Surgical Oncology and Thoracic Surgery, Department of Surgery, University Hospital Mannheim, University of Heidelberg, Germany.
  • Gronchi A; Melanoma and Sarcoma Unit, Department of Surgery, Istituto Nazionale Tumori, Milan, Italy. Electronic address: alessandro.gronchi@istitutotumori.mi.it.
Ann Oncol ; 21(2): 403-408, 2010 Feb.
Article in En | MEDLINE | ID: mdl-19628568
ABSTRACT

BACKGROUND:

Surgical indication for metastatic gastrointestinal stromal tumor (GIST) treated with imatinib is not yet established. MATERIALS AND

METHODS:

We analyzed 80 patients who underwent surgery for metastatic GIST after imatinib therapy from July 2002 to October 2007. Patients were divided into those with surgery at best clinical response (group A, n = 49) and those with surgery at focal progression (group B, n = 31). Primary end points were progression-free survival (PFS) and disease-specific survival (DSS).

RESULTS:

Two-year postoperative PFS was 64.4% in group A and 9.7% in group B (P < 0.01). In group A, median PFS was not reached; in group B, it was 8 months. Median DSS from the time of imatinib onset was not reached in either group. Five-year DSS was 82.9% in group A and 67.6% in group B (P < 0.01). Multivariate analysis confirmed a significantly shorter PFS and DSS in group B. Surgical morbidity occurred in 13 patients (16.3%).

CONCLUSIONS:

Surgery for focal progressive lesions could be considered as part of the second-line/third-line armamentarium in selected cases. Surgery of residual disease upon best clinical response seems associated with survival benefit compared with historical controls in similar patient collectives treated with imatinib alone. However, evidence from prospective randomized trials is needed to make definite recommendations.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piperazines / Pyrimidines / Gastrointestinal Stromal Tumors Type of study: Evaluation_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Ann Oncol Year: 2010 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piperazines / Pyrimidines / Gastrointestinal Stromal Tumors Type of study: Evaluation_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Ann Oncol Year: 2010 Document type: Article