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. 2008 Jan 23;2008(1):CD004024. doi: 10.1002/14651858.CD004024.pub2

5. Patients in experimental arm who underwent HD and SCT (%).

Study % HD and SCT Reasons for not
De Souza 18/28 (64%) 3x refusal, 7x death
Martelli 2003 45/75 (60%) 7x refusal, 2x inadequate collection , 12x early progression, 1x death, 3x low performance status, 1x thrombosis/embolic event, 1x BM involvement, 1x ulcer perforation, 1x hyperglycaemic coma, 1x acute occlusion femoral artery
Gianni 48/48 (100%) all patients received HDT
Gisselbrecht 139/189 (74%) 24x progression, 3x refusal, 9x severe toxicity during induction, 8x death, 6x miscellaneous
Haioun 198/268 (74%) "most commonly refusal or early relapse"
Intragumtornchai 14/23 (61%) 5x death, 2x refusal, 2x "protocol violation"
Kaiser 103/158 (65%) 19x lack of response/progression, 14x refusal, 4x concomitant disease, 5x toxicity of induction, 2x collection failure, 7x others, 3x death
Kluin‐Nelemans 60/98 (61%) 12x relapse/progression, 6x toxicity, 15x refusal, 5x lost to FU/no data
Martelli 1996 22/29 (76%) 3x progression, 1x refusal, 2x medical decision, 1x protocol violation
Milpied 83/98 (85%) 13x: progression or no PR and CR
Rodriguez 2003 44/59 (75%) not reported
Santini 1998 45/63 (71%) 1x ineligible, 2x death, 5x refusal, 10x progression
Santini 2003 79/117 (68%) 10x refusal, 7x toxicity, 14x progressive disease or death, 5x ineligible, 1x lost to follow‐up, 1x protocol violation
Verdonck 26/34 (76%) 5x progression, 3x refusal
Vitolo 50/60 (83%)
Haioun (subgroup) 86/125 (69%)