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A pharmacometric analysis of patient-reported outcomes in breast cancer patients through item response theory

Schindler, Emilie (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Friberg, Lena (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Lum, Bertram L. (author)
Genentech Inc, South San Francisco, CA USA
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Wang, Bei (author)
Genentech Inc, South San Francisco, CA USA
Quartino, Angelica (author)
Genentech Inc, South San Francisco, CA USA
Li, Chunze (author)
Genentech Inc, South San Francisco, CA USA
Girish, Sandhya (author)
Genentech Inc, South San Francisco, CA USA
Jin, Jin Y. (author)
Genentech Inc, South San Francisco, CA USA
Karlsson, Mats O. (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
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 (creator_code:org_t)
2018-04-19
2018
English.
In: Pharmaceutical research. - : Springer Science and Business Media LLC. - 0724-8741 .- 1573-904X. ; 35:6
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • PurposeAn item response theory (IRT) pharmacometric framework is presented to characterize Functional Assessment of Cancer Therapy-Breast (FACT-B) data in locally-advanced or metastatic breast cancer patients treated with ado-trastuzumab emtansine (T-DM1) or capecitabine-plus-lapatinib.MethodsIn the IRT model, four latent well-being variables, based on FACT-B general subscales, were used to describe the physical, social/family, emotional and functional well-being. Each breast cancer subscale item was reassigned to one of the other subscales. Longitudinal changes in FACT-B responses and covariate effects were investigated.ResultsThe IRT model could describe both item-level and subscale-level FACT-B data. Non-Asian patients showed better baseline social/family and functional well-being than Asian patients. Moreover, patients with Eastern Cooperative Oncology Group performance status of 0 had better baseline physical and functional well-being. Well-being was described as initially increasing or decreasing before reaching a steady-state, which varied substantially between patients and subscales. T-DM1 exposure was not related to any of the latent variables. Physical well-being worsening was identified in capecitabine-plus-lapatinib-treated patients, whereas T-DM1-treated patients typically stayed stable.ConclusionThe developed framework provides a thorough description of FACT-B longitudinal data. It acknowledges the multi-dimensional nature of the questionnaire and allows covariate and exposure effects to be evaluated on responses.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Keyword

ado-trastuzumab emtansine
capecitabine
kadcyla
lapatinib
nonlinear mixed effects
NONMEM
T-DM1

Publication and Content Type

ref (subject category)
art (subject category)

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