Summary of studies examining QOL after HCT
. | QOL index . | Patients . | Data collected . | Time points . | Outcomes . | Comparator . | Special considerations . |
---|---|---|---|---|---|---|---|
Syrjala et al 199329 | SIP | HCT, N = 67 | Prospective | Baseline, d 90, and 1 y after HCT |
| Baseline levels compared with population norms |
|
Kopp et al 199898 | FACT BMT and EORTC QLQ C30 | HCT, N = 56 | Prospective | 1y, 2y | Reduced QOL at 1y, improved by 2y | None | |
McQuellon et al 199823 | FACT-BMT | HCT, N = 86 | Prospective | Baseline, hospital discharge, d 100, 1y | Overall QOL trend parabolic; worsened by discharge, then improved by d100 and 1y | None |
|
Hjermstad et al 199961 | EORTC QLQ-C30 | HCT, N = 177 | Prospective | 1 y after HCT | Significantly worse social, role function, appetite loss, financial difficulty, cognition, physical role | Reference data from general population sample | |
Uses a subset of the Hjermstad et al 199916 | EORTC QLQ-C30 | HCT and chemo SCT, n = 41; ASCT, n = 51; CT, n = 85 | Prospective | Baseline, 1 y after HCT |
| HCT group compared with chemo group as control | |
Bush et al 200026 | EORTC QLQ C30 | HCT, N = 415 | Prospective | Annual, 1 y through 4 y |
| None | |
Lee et al 200122 | Questionnaires developed for the study | HCT, N = 320 | Prospective | Baseline, 6, 12, 24 mo |
| Auto and allo HCT | More complete recovery in Auto HCT group at 6 mo, but equalized by 12 mo |
Díez-Campelo et al 200457 | FACT-BMT | RIC Allo HCT, N = 47 | Prospective | D 7, 14, 21, 90, 180, 270, 360 | RIC Allo HCT scores significantly better compared with auto HCT early in course | Comparison group of auto HCT | |
Hjermstad et al 200417 | EORTC-QLQ-C30 | HCT, and chemo SCT, n = 61; ASCT, n = 69; CT, n = 118 | Prospective | 3-5 y after HCT | Allo group reported improvement in overall QOL from 1 y to 3-5 y, worse role functioning and fatigue than population norms | Reference data from general population sample | Hjermstad et al 199916 |
Syrjala et al 20042 | SIP | HCT, N = 319 | Prospective | Pre-HCT, d 90; 1, 3, 5 y |
| Auto and allo HCT | |
Bevans et al 200624 | SF-36, and FACT-BMT | Allo HCT (ablative vs RIC), n = 41 (RIC), n = 35 (ablative) | Prospective | Baseline, d 0, 30, 100, 1 y, 2 y |
| Ablative vs RIC allo HCT | |
Lee et al 20068 | FACT-BMT | Allo HCT, N = 96 | Prospective | Baseline, 6 mo, 12 mo |
| None | |
Wettergren et al 200865 | QLQ-C30 | HCT, N = 22 | Prospective | Baseline, 1y after HCT |
| Swedish norm values (for QLQ-C30) | Included positive aspects, eg, a changed view of life and oneself |
Baker et al 199199 | SLDS | HCT, N = 135 | Cross-sectional | Single measure, > 6 mo after HCT | Role retention significantly correlated w/ quality of life | None | |
Wingard et al 199183 | Health perception scale | HCT, N = 135 | Cross-sectional | Single measure, mean 47 mo after HCT |
| None | |
Schmidt et al 199384 | COH-QOL | HCT, N = 212 | Cross-sectional | Single measure | Majority self-report 8 or greater on scale of 1–10 | None | Nonsignificantly better QOL scores in <18-year-old group vs >18-year-old group |
Baker et al 199448 | SLDS | HCT, N = 135 | Cross-sectional | Single measure, 6-149 mo after HCT |
| General population comparator | Identified several predictors of QOL: self-esteem, physical functioning, social support, graft vs host disease |
Litwins et al 199439 | SIP | HCT, N = 32 | Cross-sectional | Single measure, > 1y after treatment | No significant differences between HCT and chemotherapy | HCT (n = 32) vs chemotherapy (n = 22) | |
Andrykowski et al 199558 | SIP, ROF, PHQ, PQOL, SER | HCT, N = 200 | Cross-sectional | Single measure, mean 43 mo | QOL worse in Allo-HCT compared with Auto-HCT | Allo vs auto HCT | Predictors of reduced QOL: greater age at BMT, lower education, advanced disease at BMT |
Bush et al 199552 | EORTC QLQ C-30 | HCT, N = 125 | Cross-sectional | 6-18 y after HCT (mean 10 y) |
| Cancer and population norms | 88% state benefit of HCT outweigh the risks |
Molassiotis et al 199538 | RSCL | Allo HCT, N =50 | Cross-sectional | Mean 42.4 mo after HCT |
| Allo HCT vs Auto HCT | Physical symptoms, adjustment to vocational environment, and depression were predictors for QOL |
Molassiotis et al 199637 | RSCL, PSFQ | HCT, N = 91 | Cross-sectional | Mean 39.8 mo after HCT | 79.6% report ″good to excellent″ QOL; no significant difference between HCT and chemotherapy group | HCT (n = 91) vs chemotherapy (n = 73) | |
Prieto et al 199640 | NHP, GHQ | HCT, N = 117 | Cross-sectional | Single assessment, median 55 mo |
|
| Multivariate analyses: higher systemic symptom score, lower educational level, older age, shorter time after BMT, female sex, and impotence significant predictors of impaired overall QOL |
Wellisch et al 199642 | CARES | Allo-HCT for AML, N = 30 | Cross-sectional | Single measure 5-6.5 y after therapy | No significant differences in QOL comparing HCT and chemotherapy | Consolidation chemotherapy | |
Sutherland et al 199749 | SF-36, SLDS-BMT | Allo HCT, N = 231 | Cross-sectional | Single assessment, median 40 mo |
| Age adjusted population norms | |
Zittoun et al 199735 | EORTC QLQ C30 | Allo vs auto vs chemo in AML in CR1, N = 98 | Cross-sectional | Single measure, median time 53 mo after CR | Significantly lower QOL scores (allogeneic < autologous < chemotherapy) | Examined allo HCT vs auto vs after remission chemotherapy | |
Edman et al 200151 | SIP | Allo HCT, N = 25 | Cross-sectional | Single measure, 2-4 y after HCT |
| Swedish population norms | Despite impairments, 80% report general health good or excellent |
Heinonen et al 2001100 | FACT-BMT | Allo HCT, N = 109 | Cross-sectional | Single measure, minimum follow up 4 mo | No significant differences between males and females in overall physical, functional, and social well-being by the FACT-BMT | Compared men with women in study sample |
|
Kiss et al 200247 | MOS-SF36, SLDS-BMT | Allo HCT in CML, N = 89 | Cross-sectional | 10 y after HCT | Significant reductions in physical functioning and general health | US normative population | cGVHD significant predictor of QOL |
Worel et al 200255 | EORTC QLQ-C30 | Allo or syngeneic HCT, N = 106 | Cross-sectional | Single measure, >2y after HCT | Demonstrated significant worsening in QLQ-C30 scores for those with cGVHD (compared with those without) | None | |
Wong et al 200356 | FACT-BMT | RIC Allo HCT, N = 9 | Cross-sectional | Single measure, median of 495 to 910 d after HCT | Reported good QOL, median FACT-BMT score 147.19 | None | |
Hayden et al 200450 | EORTC QLQ-C30 | Allo HCT in CML, N = 46 | Cross-sectional | Single measure, median 98 mo | No difference in the Physical, Emotional and Social domains or overall Global Health Status/QOL-scores significantly lower for role, cognitive function | Age adjusted general population |
|
Andrykowski et al 200520 | SF-36 | HCT, N = 662 | Cross-sectional | Single measure mean 7y after HCT | HCT group: significantly worse physical health, physical functioning, social functioning, psychologic adjustment, and dyadic adjustment | Healthy age, sex matched controls, n = 158 | HCT group had more psychologic and interpersonal growth |
Kopp et al 200544 | EORTC-QLQ C30 | HCT, N = 34 | Cross-sectional | Single measure (>5y after HCT) | Significantly lower QOL on the dimensions of physical and social functioning and on the financial impact symptom scale | 68 age, sex, race matched healthy controls | |
Syrjala et al 200545 | SF-36 | Allo HCT, N = 137(supp) | Cross-sectional | Single measure at 10y after HCT |
| 137 age-, sex-, race-matched controls | |
Fraser et al 200654 | BMT-SS | Allo HCT, N = 584 | Cross-sectional | Single measure (>2y after HCT) |
| Resolved chronic GVHD or no history of chronic GVHD | |
Messerer et al 200841 | EORTC QLQ-C30 | HCT vs CT in AML, N = 419 | Cross-sectional | Single measure, median 8y | All QLQ-C30 functions, except physical functioning and pain, were poorer in allo HCT compared with CT | Compared HCT with chemotherapy in AML |
. | QOL index . | Patients . | Data collected . | Time points . | Outcomes . | Comparator . | Special considerations . |
---|---|---|---|---|---|---|---|
Syrjala et al 199329 | SIP | HCT, N = 67 | Prospective | Baseline, d 90, and 1 y after HCT |
| Baseline levels compared with population norms |
|
Kopp et al 199898 | FACT BMT and EORTC QLQ C30 | HCT, N = 56 | Prospective | 1y, 2y | Reduced QOL at 1y, improved by 2y | None | |
McQuellon et al 199823 | FACT-BMT | HCT, N = 86 | Prospective | Baseline, hospital discharge, d 100, 1y | Overall QOL trend parabolic; worsened by discharge, then improved by d100 and 1y | None |
|
Hjermstad et al 199961 | EORTC QLQ-C30 | HCT, N = 177 | Prospective | 1 y after HCT | Significantly worse social, role function, appetite loss, financial difficulty, cognition, physical role | Reference data from general population sample | |
Uses a subset of the Hjermstad et al 199916 | EORTC QLQ-C30 | HCT and chemo SCT, n = 41; ASCT, n = 51; CT, n = 85 | Prospective | Baseline, 1 y after HCT |
| HCT group compared with chemo group as control | |
Bush et al 200026 | EORTC QLQ C30 | HCT, N = 415 | Prospective | Annual, 1 y through 4 y |
| None | |
Lee et al 200122 | Questionnaires developed for the study | HCT, N = 320 | Prospective | Baseline, 6, 12, 24 mo |
| Auto and allo HCT | More complete recovery in Auto HCT group at 6 mo, but equalized by 12 mo |
Díez-Campelo et al 200457 | FACT-BMT | RIC Allo HCT, N = 47 | Prospective | D 7, 14, 21, 90, 180, 270, 360 | RIC Allo HCT scores significantly better compared with auto HCT early in course | Comparison group of auto HCT | |
Hjermstad et al 200417 | EORTC-QLQ-C30 | HCT, and chemo SCT, n = 61; ASCT, n = 69; CT, n = 118 | Prospective | 3-5 y after HCT | Allo group reported improvement in overall QOL from 1 y to 3-5 y, worse role functioning and fatigue than population norms | Reference data from general population sample | Hjermstad et al 199916 |
Syrjala et al 20042 | SIP | HCT, N = 319 | Prospective | Pre-HCT, d 90; 1, 3, 5 y |
| Auto and allo HCT | |
Bevans et al 200624 | SF-36, and FACT-BMT | Allo HCT (ablative vs RIC), n = 41 (RIC), n = 35 (ablative) | Prospective | Baseline, d 0, 30, 100, 1 y, 2 y |
| Ablative vs RIC allo HCT | |
Lee et al 20068 | FACT-BMT | Allo HCT, N = 96 | Prospective | Baseline, 6 mo, 12 mo |
| None | |
Wettergren et al 200865 | QLQ-C30 | HCT, N = 22 | Prospective | Baseline, 1y after HCT |
| Swedish norm values (for QLQ-C30) | Included positive aspects, eg, a changed view of life and oneself |
Baker et al 199199 | SLDS | HCT, N = 135 | Cross-sectional | Single measure, > 6 mo after HCT | Role retention significantly correlated w/ quality of life | None | |
Wingard et al 199183 | Health perception scale | HCT, N = 135 | Cross-sectional | Single measure, mean 47 mo after HCT |
| None | |
Schmidt et al 199384 | COH-QOL | HCT, N = 212 | Cross-sectional | Single measure | Majority self-report 8 or greater on scale of 1–10 | None | Nonsignificantly better QOL scores in <18-year-old group vs >18-year-old group |
Baker et al 199448 | SLDS | HCT, N = 135 | Cross-sectional | Single measure, 6-149 mo after HCT |
| General population comparator | Identified several predictors of QOL: self-esteem, physical functioning, social support, graft vs host disease |
Litwins et al 199439 | SIP | HCT, N = 32 | Cross-sectional | Single measure, > 1y after treatment | No significant differences between HCT and chemotherapy | HCT (n = 32) vs chemotherapy (n = 22) | |
Andrykowski et al 199558 | SIP, ROF, PHQ, PQOL, SER | HCT, N = 200 | Cross-sectional | Single measure, mean 43 mo | QOL worse in Allo-HCT compared with Auto-HCT | Allo vs auto HCT | Predictors of reduced QOL: greater age at BMT, lower education, advanced disease at BMT |
Bush et al 199552 | EORTC QLQ C-30 | HCT, N = 125 | Cross-sectional | 6-18 y after HCT (mean 10 y) |
| Cancer and population norms | 88% state benefit of HCT outweigh the risks |
Molassiotis et al 199538 | RSCL | Allo HCT, N =50 | Cross-sectional | Mean 42.4 mo after HCT |
| Allo HCT vs Auto HCT | Physical symptoms, adjustment to vocational environment, and depression were predictors for QOL |
Molassiotis et al 199637 | RSCL, PSFQ | HCT, N = 91 | Cross-sectional | Mean 39.8 mo after HCT | 79.6% report ″good to excellent″ QOL; no significant difference between HCT and chemotherapy group | HCT (n = 91) vs chemotherapy (n = 73) | |
Prieto et al 199640 | NHP, GHQ | HCT, N = 117 | Cross-sectional | Single assessment, median 55 mo |
|
| Multivariate analyses: higher systemic symptom score, lower educational level, older age, shorter time after BMT, female sex, and impotence significant predictors of impaired overall QOL |
Wellisch et al 199642 | CARES | Allo-HCT for AML, N = 30 | Cross-sectional | Single measure 5-6.5 y after therapy | No significant differences in QOL comparing HCT and chemotherapy | Consolidation chemotherapy | |
Sutherland et al 199749 | SF-36, SLDS-BMT | Allo HCT, N = 231 | Cross-sectional | Single assessment, median 40 mo |
| Age adjusted population norms | |
Zittoun et al 199735 | EORTC QLQ C30 | Allo vs auto vs chemo in AML in CR1, N = 98 | Cross-sectional | Single measure, median time 53 mo after CR | Significantly lower QOL scores (allogeneic < autologous < chemotherapy) | Examined allo HCT vs auto vs after remission chemotherapy | |
Edman et al 200151 | SIP | Allo HCT, N = 25 | Cross-sectional | Single measure, 2-4 y after HCT |
| Swedish population norms | Despite impairments, 80% report general health good or excellent |
Heinonen et al 2001100 | FACT-BMT | Allo HCT, N = 109 | Cross-sectional | Single measure, minimum follow up 4 mo | No significant differences between males and females in overall physical, functional, and social well-being by the FACT-BMT | Compared men with women in study sample |
|
Kiss et al 200247 | MOS-SF36, SLDS-BMT | Allo HCT in CML, N = 89 | Cross-sectional | 10 y after HCT | Significant reductions in physical functioning and general health | US normative population | cGVHD significant predictor of QOL |
Worel et al 200255 | EORTC QLQ-C30 | Allo or syngeneic HCT, N = 106 | Cross-sectional | Single measure, >2y after HCT | Demonstrated significant worsening in QLQ-C30 scores for those with cGVHD (compared with those without) | None | |
Wong et al 200356 | FACT-BMT | RIC Allo HCT, N = 9 | Cross-sectional | Single measure, median of 495 to 910 d after HCT | Reported good QOL, median FACT-BMT score 147.19 | None | |
Hayden et al 200450 | EORTC QLQ-C30 | Allo HCT in CML, N = 46 | Cross-sectional | Single measure, median 98 mo | No difference in the Physical, Emotional and Social domains or overall Global Health Status/QOL-scores significantly lower for role, cognitive function | Age adjusted general population |
|
Andrykowski et al 200520 | SF-36 | HCT, N = 662 | Cross-sectional | Single measure mean 7y after HCT | HCT group: significantly worse physical health, physical functioning, social functioning, psychologic adjustment, and dyadic adjustment | Healthy age, sex matched controls, n = 158 | HCT group had more psychologic and interpersonal growth |
Kopp et al 200544 | EORTC-QLQ C30 | HCT, N = 34 | Cross-sectional | Single measure (>5y after HCT) | Significantly lower QOL on the dimensions of physical and social functioning and on the financial impact symptom scale | 68 age, sex, race matched healthy controls | |
Syrjala et al 200545 | SF-36 | Allo HCT, N = 137(supp) | Cross-sectional | Single measure at 10y after HCT |
| 137 age-, sex-, race-matched controls | |
Fraser et al 200654 | BMT-SS | Allo HCT, N = 584 | Cross-sectional | Single measure (>2y after HCT) |
| Resolved chronic GVHD or no history of chronic GVHD | |
Messerer et al 200841 | EORTC QLQ-C30 | HCT vs CT in AML, N = 419 | Cross-sectional | Single measure, median 8y | All QLQ-C30 functions, except physical functioning and pain, were poorer in allo HCT compared with CT | Compared HCT with chemotherapy in AML |
HCT indicates hematopoietic cell transplantation (composite of allogeneic and autologous transplantation); auto HCT, autologous hematopoietic cell transplantation; allo HCT, allogeneic hematopoietic cell transplantation; RIC, reduced intensity conditioning regimen; CT, chemotherapy; and AML, acute myeloid leukemia.