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Table 3. Details of Included Studies
Study No. |
First Author, Year |
Phase |
Report Type |
Quality |
Comments |
Imatinib Efficacy Studies |
1 |
van Oosterom, 20016 |
I/II |
Full report |
3/5 |
Main results |
1 |
van Oosterom, 200245 |
III |
Full report |
3/5 |
Followup efficacy data for van Oosterom, et al. 2001 |
2 |
Demetri, 200246 |
II |
Full report |
5/5 |
Main results |
2 |
Dagher 200243 |
II |
Full report |
5/5 |
FDA approval summary with review of Demetri, et al. 2002 data |
2 |
Heinrich, 200347 |
II |
Full report |
6/6 |
followup efficacy data for Demetri, et al. 2002 |
3 |
Verweij, 200348 |
II |
Full report |
6/6 |
Main results |
4 |
Verweij, 200449 |
III |
Full report |
6/6 |
Main results |
4 |
Zalcberg, 200450 |
II |
Abstract |
Unk |
Followup efficacy data for Verweij, et al. 2004 |
5 |
Casali, 200451 |
II |
Abstract |
Unk |
Early results of phase II trial |
6 |
Blay, 200452 |
III |
Abstract |
Unk |
Early results of phase III trial |
7 |
Rankin, 200453 |
III |
Abstract |
Unk |
Early results of phase III trial |
7 |
Patel, 200354 |
III |
Abstract (published 2003 abstract plus commentary) |
Unk |
Early results of Rankin, et al. 2004 Phase
III trial |
Imatinib Plus Surgery Efficacy Studies |
8 |
Bumming, 200355 |
II |
Full report |
4/6 |
Main results |
9 |
Rutkowski, 200356 |
Retro |
Full report |
1/6 |
Main results |
10 |
Scaife, 200357 |
Retro |
Full report |
2/5 |
Main results |
11 |
Wu, 200358 |
Retro |
Full report |
1/6 |
Main results |
Adverse Events/harm |
1 |
van Oosterom, 20016 |
I/II |
Full report |
3/5 |
Adverse event data reported within main
results full report |
1 |
van Oosterom, 200245 |
III |
Full report |
3/5 |
followup adverse event data for van Oosterom, et al. 2001 |
2 |
Demetri, 200246 |
II |
Full report |
5/5 |
Adverse event data reported within main
results full report |
2 |
Dagher 200243 |
II |
Full report |
5/5 |
FDA approval summary with review of Demetri, et al. 2002 data |
3 |
Verweij, 200348 |
II |
Full report |
6/6 |
Adverse event data reported within main
results full report |
4 |
Verweij, 200449 |
III |
Full report |
6/6 |
Adverse event data reported within main
results full report |
Predictors—tumor characteristics |
1 |
Debiec-Rychter, 200459 |
I/II |
Full report |
6/6 |
Molecular predictors, sub-study of van
Oosterom, et al. 2001 |
2 |
Frolov, 200360 |
II |
Full report |
1/6 |
Molecular predictors, sub-study of Demetri, et al. 2002 |
2 |
Heinrich, 200347 |
II |
Full report |
6/6 |
Molecular predictors, sub-study of Demetri, et al. 2002 |
3 |
Verweij, 200348 |
II |
Full report |
6/6 |
Other predictors reported within main
results full report |
Predictors—radiological findings |
1 |
Stroobants, 200361 |
I/II |
Full report |
4/6 |
Radiological predictors, sub-study of
van Oosterom, et al. 2001 |
12 |
Antoch, 200462 |
Pros |
Full report |
5/5 |
Radiological predictors study |
13 |
Gayed, 200463 |
Pros |
Full report |
1/5 |
Radiological predictors study |
14 |
Di Giorgi, 200464 |
Pros |
Abstract |
Unk |
Radiological predictors study |
15 |
Laussau, 200465 |
Pros |
Abstract |
Unk |
Radiological predictors study |
Predictors—other clinical factors |
2 |
Heinrich, 200347 |
II |
Full report |
6/6 |
Other predictors, sub-study of Demetri, et al. 2002 |
4 |
Verweij, 200449 |
III |
Full report |
6/6 |
Other predictors reported within main
results full report |
Abbreviations: Retro = retrospective; Unk = unknown; Pros = prospective
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