Abstract
Abstract 1322
Pre-transplant work-up prior to an allogeneic stem cell transplant (allo-SCT) generally includes pulmonary functions tests (PFT) with assessment of FEV1 and DLco. It has been previously published that patients with a DLco or FEV1 less than 60% of predicted have higher non-relapse mortality (NRM) when undergoing a myeloablative allo-SCT. However, the PFT criteria for selecting candidates for a reduced intensity (RI) allogeneic transplant allo-SCT remains poorly investigated. We performed a retrospective analysis to assess the impact of low FEV1 or DLco on NRM and overall survival (OS) in patients undergoing a RI allo-SCT.
All patients who underwent a RI allo-SCT for hematological malignancies at MD Anderson Cancer Center from Jan 2000 to April 2009 were included. Using Cox's proportional hazards regression, we compared the rate of NRM and OS between patients who had a pre-transplant FEV1 or DLco > 50% (control group) prior to a RI allo-SCT and those with FEV1 and DLco < 50% (study group). The cumulative incidence of NRM was estimated considering disease progression as a competing risk. Actuarial OS was estimated by the Kaplan-Meier method.
Patient characteristics are presented in Table 1. There were no statistically significant differences between the study and control groups except for age and sex. A significantly higher proportion of patients were > 50 years in the control group (65%) compared with the low PFT group (45%, P=0.02) and there were more males in the control group (P=.001). The median FEV1 and DLco in the study group was 55% (28-111) and 47% (33-98) of predicted, respectively. On univariate analysis abnormal PFTs did not impact OS at 30 months (HR 1.1, 95% CI 0.7–1.8, P=0.7) or NRM at 1 year (HR 1.3, (95% CI 0.6–2.7, P=0.4). Active disease at SCT, and a diagnosis of CLL, NHL or HL were associated with significantly worse OS and NRM, whereas age >50 years was only associated with worse OS. Low PFT had no significant impact on OS and NRM when evaluated separately in patients older or younger than 50 years old.
Our experience suggests that a low (<50% of predicted) FEV1 or a DLco on pre-transplant evaluation does not adversely impact NRM and OS after RI allo-SCT. These findings need to be validated in a multivariate analysis.
. | Low PFT (N, %) . | Control (N, %) . | p–value . |
---|---|---|---|
Number of patients | 33 | 774 | |
Follow–up (Median, range) months | 33 (5–95) | 28 (1–116) | |
Age, Median, years (range) | 48 (21–77) | 55 (20–77) | 0.06 |
Sex, male | 12 (36%) | 497 (64%) | 0.001 |
Active disease at RI allo-SCT | 24 (73%) | 555 (72%) | 0.9 |
Donor: | |||
MRD | 19 (58%) | 332 (43%) | 0.09 |
MUD | 13 (39%) | 373 (48%) | |
Other | 1 (3%) | 69 (9%) | |
Cell Source: | |||
Peripheral blood | 25 (76%) | 505(65%) | 0.2 |
Bone marrow | 8 (24%) | 269 (35%) | |
Diagnosis: | |||
AML/MDS/ALL/CML | 15 (48%) | 337 (43%) | 0.7 |
CLL/NHL/HL | 12 (36%) | 337 (43%) | |
MM/AA/Other | 5 (15%) | 100 (13%) |
. | Low PFT (N, %) . | Control (N, %) . | p–value . |
---|---|---|---|
Number of patients | 33 | 774 | |
Follow–up (Median, range) months | 33 (5–95) | 28 (1–116) | |
Age, Median, years (range) | 48 (21–77) | 55 (20–77) | 0.06 |
Sex, male | 12 (36%) | 497 (64%) | 0.001 |
Active disease at RI allo-SCT | 24 (73%) | 555 (72%) | 0.9 |
Donor: | |||
MRD | 19 (58%) | 332 (43%) | 0.09 |
MUD | 13 (39%) | 373 (48%) | |
Other | 1 (3%) | 69 (9%) | |
Cell Source: | |||
Peripheral blood | 25 (76%) | 505(65%) | 0.2 |
Bone marrow | 8 (24%) | 269 (35%) | |
Diagnosis: | |||
AML/MDS/ALL/CML | 15 (48%) | 337 (43%) | 0.7 |
CLL/NHL/HL | 12 (36%) | 337 (43%) | |
MM/AA/Other | 5 (15%) | 100 (13%) |
. | Low PFTs (N=33) . | Control (N=774) . | p–value . |
---|---|---|---|
% NRM | |||
3 months | 12 (95% CI 5–30) | 10 (95% CI 8–13) | 0.8 |
12 months | 25 (95% CI 13–45) | 21 (95% CI 18–25) | 0.4 |
% OS: | |||
3 months | 88 (95% CI 71–95) | 88 (95% CI 85–90) | 0.9 |
12 months | 53 (95% CI 34–68) | 62 (95% CI 58–65) | 0.3 |
. | Low PFTs (N=33) . | Control (N=774) . | p–value . |
---|---|---|---|
% NRM | |||
3 months | 12 (95% CI 5–30) | 10 (95% CI 8–13) | 0.8 |
12 months | 25 (95% CI 13–45) | 21 (95% CI 18–25) | 0.4 |
% OS: | |||
3 months | 88 (95% CI 71–95) | 88 (95% CI 85–90) | 0.9 |
12 months | 53 (95% CI 34–68) | 62 (95% CI 58–65) | 0.3 |
No relevant conflicts of interest to declare.
Author notes
Asterisk with author names denotes non-ASH members.