Table 1.
Baseline characteristics of 21 clinical trials included in the meta-analysis (Part 2)
Author | Clinical register | Year | Subgroup | Clinical status | Treatment | Patient states | Age (years), median (range) | Size |
---|---|---|---|---|---|---|---|---|
Alvarado Y12 | NA | 2014 | Multiple types | NA | Monotherapy | Prior treatments | 54 (18–87) | 69 |
Cooper TM13 | NCT01411267 | 2016 | Quizartinib | Phase I | Chemotherapy, quizartinib | Relapsed AML | ≤21 | 14 |
Cortes JE30 | NA | 2012 | Quizartinib | Phase II | Monotherapy | Relapsed/refractory AML | ≥60 | 133 |
Cortes JE14 | NCT00462761 | 2013 | Quizartinib | Phase I | Monotherapy | Relapsed/refractory AML | 60 (23–86) | 54 |
Crump M15 | NA | 2010 | Sorafenib | Phase I | Monotherapy | Relapsed/refractory AML or MDS | 71 (37–82) | 27 |
Fiedler W17 | NA | 2005 | Sunitinib | Phase I | Monotherapy | Relapsed/refractory AML | 72 (54–80) | 12 |
Fiedler W16 | NCT00783653 | 2015 | Sunitinib | Phase I/II | Chemotherapy, sunitinib | Untreated newly diagnosed AML | ≥60 | 22 |
Fischer T18,a | NCT00045942 | 2010 | Midostaurin | Phase IIB | Monotherapy | Relapsed/refractory AML or MDS | ≥18 | 92 |
Inaba H19 | NA | 2011 | Sorafenib | Phase I | Sorafenib, clofarabine, and cytarabine | Relapsed/refractory AML | ≤21 | 11 |
Knapper S20 | NA | 2006 | Lestaurtinib | Phase II | Monotherapy | Untreated AML | 73 (67–82) | 27 |
Levis MJ29 | NA | 2012 | Quizartinib | Phase II | Monotherapy | Relapsed/refractory AML | FLT3–ITD (+): 50 (19–77) FLT3–ITD (−): 55 (30–73) |
137 |
Macdonald DA21 | IND.186 | 2013 | Sorafenib | Phase I/II | Sorafenib and low-dose cytarabine | No prior chemotherapy | ≥60 | 21 |
Pratz KW11 | NA | 2010 | Sorafenib | N | Monotherapy | Relapsed/refractory AML | Median 63 | 12 |
Ramsingh G22 | NCT01161550 | 2014 | Midostaurin | Phase I | Chemotherapy and midostaurin | Relapsed/refractory AML | 52 (32–71) | 9 |
Ravandi F24,b | NA | 2010 | Sorafenib | Phase I/II | Sorafenib, idarubicin, and cytarabine | Untreated AML | ≤65 | 51 |
Ravandi F23 | NA | 2014 | Sorafenib | Phase II | Sorafenib, cytarabine, and idarubicin | Untreated AML | 53 (18–66) | 62 |
Stone RM26,c | NA | 2012 | Midostaurin | Phase IB | Midostaurin, chemotherapy | Untreated AML | Median 48.5 | 40 |
Walker AR28,d | NCT01174888 | 2016 | Midostaurin | Phase I | Midostaurin, bortezomib, and MEC | Relapsed/refractory AML | 19–70 | 23 |
Röllig C25 | NA | 2012 | Sorafenib | NA | Mixed | Mixed | 64.5 (19–82) | 28 |
Iyer SP31 | NA | 2016 | Crenolanib | NA | Crenolanib, salvage chemotherapy, and HAM | Prior treatments | 70.5 (22–90) | 6 |
Zhang W27 | CTEP25XS06801 | 2008 | Sorafenib | NA | Monotherapy | Prior treatments | 61.5 (48–81) | 16 |
Notes:
ORR=CR+PR+HI+BR defined in this article.
Only patients in Phase II included.
Only patients in dose schedule III included.
Only patients in dose levels 3, 3*, 3A, and 4 included.
Abbreviations: NA, not available; AML, acute myeloid leukemia; MDS, myelodysplastic syndrome; MEC, mitoxantrone, etoposide, cytarabine; HAM, high-dose Ara-C/mitoxantrone.