TY - JOUR
T1 - Secondary malignancies following high dose therapy and autologous hematopoietic cell transplantation-systematic review and meta-analysis
AU - Vaxman, I.
AU - Ram, R.
AU - Gafter-Gvili, A.
AU - Vidal, L.
AU - Yeshurun, M.
AU - Lahav, M.
AU - Shpilberg, O.
N1 - Publisher Copyright:
© 2015 Macmillan Publishers Limited.
PY - 2015/5/8
Y1 - 2015/5/8
N2 - We performed a systematic review and meta-analysis of randomized controlled trials comparing autologous hematopoietic cell transplantation (HCT) with other treatment modalities to analyze the risk for various secondary malignancies (SMs). Relative risks (RR) with 95% confidence intervals were estimated and pooled. Our search yielded 36 trials. The median follow-up was 55 (range 12-144) months. Overall, the RR for developing SMs was 1.23 ((0.97-1.55), I 2 =4%, 9870 patients). Subgroup analysis of trials assessing TBI-containing preparative regimens and of patients with baseline lymphoproliferative diseases, showed there was a higher risk for SMs in patients given autografts (RR=1.61 (1.05-2.48), I 2 =14%, 2218 patients and RR=1.62 (1.12-2.33), I 2 =22%, 3343 patients, respectively). Among all patients, there was a higher rate of myelodysplastic syndrome MDS/AML in patients given HCT compared with other treatments (RR=1.71 (1.18-2.48), I 2 =0%, 8778 patients). The risk of secondary solid malignancies was comparable in the short term between patients given HCT and patients given other treatments (RR=0.95 (0.67-1.32), I 2 =0%, 5925 patients). We conclude that overall the risk of secondary MDS/AML is higher in patients given autologous HCT compared with other treatments. In the subgroup of patients given a TBI-based regimen and in those with a baseline lymphoproliferative disease, there was a higher risk of overall SMs.
AB - We performed a systematic review and meta-analysis of randomized controlled trials comparing autologous hematopoietic cell transplantation (HCT) with other treatment modalities to analyze the risk for various secondary malignancies (SMs). Relative risks (RR) with 95% confidence intervals were estimated and pooled. Our search yielded 36 trials. The median follow-up was 55 (range 12-144) months. Overall, the RR for developing SMs was 1.23 ((0.97-1.55), I 2 =4%, 9870 patients). Subgroup analysis of trials assessing TBI-containing preparative regimens and of patients with baseline lymphoproliferative diseases, showed there was a higher risk for SMs in patients given autografts (RR=1.61 (1.05-2.48), I 2 =14%, 2218 patients and RR=1.62 (1.12-2.33), I 2 =22%, 3343 patients, respectively). Among all patients, there was a higher rate of myelodysplastic syndrome MDS/AML in patients given HCT compared with other treatments (RR=1.71 (1.18-2.48), I 2 =0%, 8778 patients). The risk of secondary solid malignancies was comparable in the short term between patients given HCT and patients given other treatments (RR=0.95 (0.67-1.32), I 2 =0%, 5925 patients). We conclude that overall the risk of secondary MDS/AML is higher in patients given autologous HCT compared with other treatments. In the subgroup of patients given a TBI-based regimen and in those with a baseline lymphoproliferative disease, there was a higher risk of overall SMs.
UR - http://www.scopus.com/inward/record.url?scp=84928925047&partnerID=8YFLogxK
U2 - 10.1038/bmt.2014.325
DO - 10.1038/bmt.2014.325
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C2 - 25665042
AN - SCOPUS:84928925047
SN - 0268-3369
VL - 50
SP - 706
EP - 714
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 5
ER -