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. Author manuscript; available in PMC: 2016 Aug 1.
Published in final edited form as: Biol Blood Marrow Transplant. 2015 Apr 7;21(8):1479–1487. doi: 10.1016/j.bbmt.2015.04.004

Appendix 1.

Cox regression models for associations of HCT-CI scores with risks of non-relapse (NRM) and overall mortality among recipients of autologous HCT and within subgroups of lymphoma versus multiple myeloma.

NRM Overall mortality
HCT-CI scores n HR (95% CI) P n HR (95% CI) P
Lymphoma subgroup * overall 0.043 0.001
0 1243 1.00 1264 1.00
0, but other comorbidity reported 311 0.96 (0.57–1.61) 0.863 318 0.99 (0.77–1.28) 0.959
1–2 977 1.24 (0.88–1.73) 0.218 988 1.23 (1.05–1.46) 0.013
3+ 832 1.56 (1.12–2.17) 0.009 838 1.37 (1.15–1.62) <0.0001
Myeloma subgroup * overall 0.048 <0.0001
0 1657 1.00 1949 1.00
0, but other comorbidity reported 586 0.95 (0.59–1.55) 0.844 682 0.76 (0.59–0.98) 0.032
1–2 1382 1.32 (0.93–1.87) 0.119 1620 1.39 (1.18–1.64) <0.0001
3+ 1168 1.55 (1.09–2.20) 0.015 1386 1.43 (1.21–1.69) <0.0001
*

The Cox regression models were adjusted for diagnosis category, chemo-sensitivity for lymphoma, stem cell source, KPS percentage, conditioning regimen, recipient age, recipient race, and interval between diagnosis and HCT.