Quality assessment of autografting by probability evaluation: model estimation by clinical end-points in newly diagnosed multiple myeloma patients
(2006) In Cytotherapy 8(1). p.79-88- Abstract
- Background Pre-transplant clinical evaluation of autografting is an important step in predicting post-transplant support, complications and safety. Today, unfavorable outcomes such as early death or graft failure are rare, making them unsuitable for quality assessment of supportive autografting. However, end-points constructed from frequently occurring clinical events may estimate clinically relevant prognostic models. Methods The present retrospective analysis was based on two consecutive clinical trials in the Nordic area, including up to 640 newly diagnosed multiple myeloma patients. Results In the model, the efficacy (time on antibiotics and use of transfusions) was influenced by pre-transplant variables, including sex, nationality,... (More)
- Background Pre-transplant clinical evaluation of autografting is an important step in predicting post-transplant support, complications and safety. Today, unfavorable outcomes such as early death or graft failure are rare, making them unsuitable for quality assessment of supportive autografting. However, end-points constructed from frequently occurring clinical events may estimate clinically relevant prognostic models. Methods The present retrospective analysis was based on two consecutive clinical trials in the Nordic area, including up to 640 newly diagnosed multiple myeloma patients. Results In the model, the efficacy (time on antibiotics and use of transfusions) was influenced by pre-transplant variables, including sex, nationality, serum creatinine, hemoglobin, disease stage at diagnosis, response following induction therapy, length of priming and average graft CD34(+) cell number per day of harvest. The toxicity end-point (time to blood cell recovery) was influenced by nationality, marrow plasma cell percentage, serum creatinine, M-component isotype, response to induction therapy, length of priming and graft CD34(+) cell number. The safety (early disease recurrence or death) was influenced by serum creatinine, hemoglobin, treatment response and CD34(+) cell number. Discussion In conclusion, the model illustrates that intervention strategies in quality assessment of autografting may benefit from probability estimates of graded clinical end-points. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/417535
- author
- Roer, O ; Hammerstrom, J ; Lenhoff, Stig LU ; Mylin, AK ; Knudsen, LM ; Rasmussen, T and Johnsen, HE
- organization
- publishing date
- 2006
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- translational, research, quality assessment, autografting, multiple myeloma
- in
- Cytotherapy
- volume
- 8
- issue
- 1
- pages
- 79 - 88
- publisher
- Taylor & Francis
- external identifiers
-
- pmid:16637135
- wos:000235427100010
- scopus:33344460815
- ISSN
- 1477-2566
- DOI
- 10.1080/14653240500499549
- language
- English
- LU publication?
- yes
- id
- ec394a86-acfe-460a-a15f-bc06a1050f4b (old id 417535)
- date added to LUP
- 2016-04-01 12:19:00
- date last changed
- 2022-01-27 01:56:13
@article{ec394a86-acfe-460a-a15f-bc06a1050f4b, abstract = {{Background Pre-transplant clinical evaluation of autografting is an important step in predicting post-transplant support, complications and safety. Today, unfavorable outcomes such as early death or graft failure are rare, making them unsuitable for quality assessment of supportive autografting. However, end-points constructed from frequently occurring clinical events may estimate clinically relevant prognostic models. Methods The present retrospective analysis was based on two consecutive clinical trials in the Nordic area, including up to 640 newly diagnosed multiple myeloma patients. Results In the model, the efficacy (time on antibiotics and use of transfusions) was influenced by pre-transplant variables, including sex, nationality, serum creatinine, hemoglobin, disease stage at diagnosis, response following induction therapy, length of priming and average graft CD34(+) cell number per day of harvest. The toxicity end-point (time to blood cell recovery) was influenced by nationality, marrow plasma cell percentage, serum creatinine, M-component isotype, response to induction therapy, length of priming and graft CD34(+) cell number. The safety (early disease recurrence or death) was influenced by serum creatinine, hemoglobin, treatment response and CD34(+) cell number. Discussion In conclusion, the model illustrates that intervention strategies in quality assessment of autografting may benefit from probability estimates of graded clinical end-points.}}, author = {{Roer, O and Hammerstrom, J and Lenhoff, Stig and Mylin, AK and Knudsen, LM and Rasmussen, T and Johnsen, HE}}, issn = {{1477-2566}}, keywords = {{translational; research; quality assessment; autografting; multiple myeloma}}, language = {{eng}}, number = {{1}}, pages = {{79--88}}, publisher = {{Taylor & Francis}}, series = {{Cytotherapy}}, title = {{Quality assessment of autografting by probability evaluation: model estimation by clinical end-points in newly diagnosed multiple myeloma patients}}, url = {{http://dx.doi.org/10.1080/14653240500499549}}, doi = {{10.1080/14653240500499549}}, volume = {{8}}, year = {{2006}}, }