JAMA· 2012Q1
Operabl Gastrointestinal Stromal Tümörü İçin Bir Yıllık ve Üç Yıllık Adjuvan İmatinib Karşılaştırması
One vs Three Years of Adjuvant Imatinib for Operable Gastrointestinal Stromal Tumor
- 972atıf
- Q1SCImago
- 2012yıl
Kısa özet
Adjuvan imatinibin üç yıl boyunca uygulanması, bir yıla kıyasla yüksek riskli gastrointestinal stromal tümör (GIST) hastalarında nüks-serbest sağkalımı (RFS) ve genel sağkalımı anlamlı derecede iyileştirmiştir.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Ana noktalar
- 36 aylık adjuvan imatinib, yüksek riskli GIST hastalarında 12 aya kıyasla nüks-serbest sağkalımı (RFS) %54 oranında iyileştirmiştir (HR, 0.46; P < .001).
- 36 ay imatinib ile 5 yıllık RFS %65.6 iken, 12 ay ile %47.9'dur.
- Genel sağkalım da 36 ay imatinib ile anlamlı derecede iyileşmiştir (HR, 0.45; P = .02).
- 36 aylık imatinib grubundaki hastaların %25.8'i, 12 aylık grubundaki %12.6'ya kıyasla nüks dışı nedenlerle tedaviyi bırakmıştır.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
CONTEXT: Adjuvant imatinib administered for 12 months after surgery has improved recurrence-free survival (RFS) of patients with operable gastrointestinal stromal tumor (GIST) compared with placebo. OBJECTIVE: To investigate the role of imatinib administration duration as adjuvant treatment of patients who have a high estimated risk for GIST recurrence after surgery. DESIGN, SETTING, AND PATIENTS: Patients with KIT-positive GIST removed at surgery were entered between February 2004 and September 2008 to this randomized, open-label phase 3 study conducted in 24 hospitals in Finland, Germany, Norway, and Sweden. The risk of GIST recurrence was estimated using the modified National Institutes of Health Consensus Criteria. INTERVENTION: Imatinib, 400 mg per day, orally for either 12 months or 36 months, started within 12 weeks of surgery. MAIN OUTCOME MEASURES: The primary end point was RFS; the secondary end points included overall survival and treatment safety. RESULTS: Two hundred patients were allocated to each group. The median follow-up time after randomization was 54 months in December 2010. Diagnosis of GIST was confirmed in 382 of 397 patients (96%) in the intention-to-treat population at a central pathology review. KIT or PDGFRA mutation was detected in 333 of 366 tumors (91%) available for testing. Patients assigned for 36 months of imatinib had longer RFS compared with those assigned for 12 months (hazard ratio [HR], 0.46; 95% CI, 0.32-0.65; P < .001; 5-year RFS, 65.6% vs 47.9%, respectively) and longer overall survival (HR, 0.45; 95% CI, 0.22-0.89; P = .02; 5-year survival, 92.0% vs 81.7%). Imatinib was generally well tolerated, but 12.6% and 25.8% of patients assigned to the 12- and 36-month groups, respectively, discontinued imatinib for a reason other than GIST recurrence. CONCLUSION: Compared with 12 months of adjuvant imatinib, 36 months of imatinib improved RFS and overall survival of GIST patients with a high risk of GIST recurrence. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT00116935.
Yazarların özeti; kaynağından alınmıştır. JAMA, 2012 · DOI ↗
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Alan: Gastroenteroloji
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