Literature DB >> 9676550

Measuring health-related quality of life in clinical trials that evaluate the role of chemotherapy in cancer treatment.

M Michael1, I F Tannock.   

Abstract

Quality of life is a subjective multidimentional concept that can be assessed by means of validated questionnaires completed by patients. The psychological effects of a diagnosis of cancer and the physical effects of the disease and its treating have a major impact on a patient's health-related quality of life. Much cancer treatment, especially chemotherapy for metastatic disease, is given for palliation. Palliation implies improvement in either the duration or quality of life remaining. However, treatment patients with common metastatic tumours to prolong life is generally unsuccessful, so improving quality of life is a more realistic goal. Most trials involve evaluating shrinkage of a tumour (i.e., tumour response), which does not imply a benefit to the patient. Few trials have assessed quality of life directly, although several validated instruments, described here, are available to quantify quality of life in cancer patients. These instruments represent a wide scope, from evaluating general health to assessing the quality of life of patients with specific types and stages of cancer. They respond to changes in clinical state and are strongly predictive of survival. Measures of quality of life should be incorporated in all clinical trials where treatment is palliative, and a simple, relevant measure of quality of life should be used as a (or the) primary outcome measure. Other measures of quality of life are important to ensure that gains in one area do not occur at the expense of others. A few large trials incorporating these principles have shown that chemotherapy can provide palliation for patients with advanced cancer.

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Mesh:

Year:  1998        PMID: 9676550      PMCID: PMC1229445     

Source DB:  PubMed          Journal:  CMAJ        ISSN: 0820-3946            Impact factor:   8.262


  54 in total

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  14 in total

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Journal:  J Med Ethics       Date:  2002-12       Impact factor: 2.903

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Journal:  CMAJ       Date:  1998-10-06       Impact factor: 8.262

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Review 4.  Quality of life in children with adverse drug reactions: a narrative and systematic review.

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Journal:  Heart       Date:  2005-09       Impact factor: 5.994

Review 6.  Reporting and interpretation of SF-36 outcomes in randomised trials: systematic review.

Authors:  Despina G Contopoulos-Ioannidis; Anastasia Karvouni; Ioanna Kouri; John P A Ioannidis
Journal:  BMJ       Date:  2009-01-12

7.  Linguistic adaptation and validation of the Spanish version of the Memorial Pain Assessment Card (MPAC).

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Journal:  Clin Transl Oncol       Date:  2009-06       Impact factor: 3.405

Review 8.  Novel strategies in immune checkpoint inhibitor drug development: How far are we from the paradigm shift?

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9.  The Australia-modified Karnofsky Performance Status (AKPS) scale: a revised scale for contemporary palliative care clinical practice [ISRCTN81117481].

Authors:  Amy P Abernethy; Tania Shelby-James; Belinda S Fazekas; David Woods; David C Currow
Journal:  BMC Palliat Care       Date:  2005-11-12       Impact factor: 3.234

10.  Electronic monitoring of symptoms and syndromes associated with cancer: methods of a randomized controlled trial SAKK 95/06 E-MOSAIC.

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