Literature DB >> 16482448

Understanding cancer patients' experience and outcomes: development and pilot study of the Cancer Care Outcomes Research and Surveillance patient survey.

Jennifer L Malin1, Clifford Ko, John Z Ayanian, David Harrington, David R Nerenz, Katherine L Kahn, Julie Ganther-Urmie, Paul J Catalano, Alan M Zaslavsky, Robert B Wallace, Edward Guadagnoli, Neeraj K Arora, Maryse D Roudier, Patricia A Ganz.   

Abstract

GOALS OF WORK: The National Cancer Institute's Cancer Care Outcomes Research and Surveillance (CanCORS) Consortium is conducting a population-based study of newly diagnosed patients with lung and colorectal cancer to describe the experience of persons living with cancer and to understand which barriers present the most significant obstacles to their receipt of appropriate care. The keystone to this effort is the baseline patient survey administered approximately 4 months after diagnosis. PATIENTS AND METHODS: We developed a survey to obtain information from patients newly diagnosed with lung and colorectal cancer about their personal characteristics, decision making, experience of care, and outcomes. We conducted a pilot study to evaluate the feasibility of a lengthy and clinically detailed interview in a convenience sample of patients within 8 months of diagnosis (n=71). MAIN
RESULTS: The median length of the interviews was 75 min for patients with lung cancer (range 43-130) and 82 min for patients with colorectal cancer (range 46-119). Most patients had received some form of treatment for their cancer: 66.1% had undergone surgery, 28.2% had received radiation therapy, and 54.9% were treated with chemotherapy. In addition, 26.7% reported their overall health was less than 70 on a 0-100 scale, demonstrating that patients with substantial health impairment were able to complete the survey.
CONCLUSIONS: A clinically detailed survey of newly diagnosed lung and colorectal cancer patients is feasible. A modified version of this survey is being fielded by the CanCORS Consortium and should provide much needed population-based data regarding patients' experiences across the continuum of cancer care and their outcomes.

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Year:  2006        PMID: 16482448     DOI: 10.1007/s00520-005-0902-8

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  45 in total

1.  The construction and testing of the EORTC colorectal cancer-specific quality of life questionnaire module (QLQ-CR38). European Organization for Research and Treatment of Cancer Study Group on Quality of Life.

Authors:  M A Sprangers; A te Velde; N K Aaronson
Journal:  Eur J Cancer       Date:  1999-02       Impact factor: 9.162

2.  Racial differences in the treatment of early-stage lung cancer.

Authors:  P B Bach; L D Cramer; J L Warren; C B Begg
Journal:  N Engl J Med       Date:  1999-10-14       Impact factor: 91.245

3.  Psychometric properties of the CAHPS 1.0 survey measures. Consumer Assessment of Health Plans Study.

Authors:  R D Hays; J A Shaul; V S Williams; J S Lubalin; L D Harris-Kojetin; S F Sweeny; P D Cleary
Journal:  Med Care       Date:  1999-03       Impact factor: 2.983

Review 4.  Racial and ethnic disparities in the receipt of cancer treatment.

Authors:  Vickie L Shavers; Martin L Brown
Journal:  J Natl Cancer Inst       Date:  2002-03-06       Impact factor: 13.506

5.  Cancer survivorship--United States, 1971-2001.

Authors: 
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2004-06-25       Impact factor: 17.586

Review 6.  Quality of life: what is it? How should it be measured?

Authors:  N K Aaronson
Journal:  Oncology (Williston Park)       Date:  1988-05       Impact factor: 2.990

7.  Age and adjuvant chemotherapy use after surgery for stage III colon cancer.

Authors:  D Schrag; L D Cramer; P B Bach; C B Begg
Journal:  J Natl Cancer Inst       Date:  2001-06-06       Impact factor: 13.506

8.  Age, sex, and racial differences in the use of standard adjuvant therapy for colorectal cancer.

Authors:  Arnold L Potosky; Linda C Harlan; Richard S Kaplan; Karen A Johnson; Charles F Lynch
Journal:  J Clin Oncol       Date:  2002-03-01       Impact factor: 44.544

9.  Prevalence of overweight and obesity among US children, adolescents, and adults, 1999-2002.

Authors:  Allison A Hedley; Cynthia L Ogden; Clifford L Johnson; Margaret D Carroll; Lester R Curtin; Katherine M Flegal
Journal:  JAMA       Date:  2004-06-16       Impact factor: 56.272

10.  Decreasing variation in the use of hospice among older adults with breast, colorectal, lung, and prostate cancer.

Authors:  Nuha A Lackan; Glenn V Ostir; Jean L Freeman; Jonathan D Mahnken; James S Goodwin
Journal:  Med Care       Date:  2004-02       Impact factor: 2.983

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  81 in total

1.  Who provides psychosocial follow-up care for post-treatment cancer survivors? A survey of medical oncologists and primary care physicians.

Authors:  Laura P Forsythe; Catherine M Alfano; Corinne R Leach; Patricia A Ganz; Michael E Stefanek; Julia H Rowland
Journal:  J Clin Oncol       Date:  2012-07-09       Impact factor: 44.544

2.  A snapshot of smokers after lung and colorectal cancer diagnosis.

Authors:  Elyse R Park; Sandra J Japuntich; Nancy A Rigotti; Lara Traeger; Yulei He; Robert B Wallace; Jennifer L Malin; Jennifer P Zallen; Nancy L Keating
Journal:  Cancer       Date:  2012-01-23       Impact factor: 6.860

3.  Do depressed newly diagnosed cancer patients differentially benefit from nurse navigation?

Authors:  Evette J Ludman; Ruth McCorkle; Erin Aiello Bowles; Carolyn M Rutter; Jessica Chubak; Leah Tuzzio; Salene Jones; Robert J Reid; Robert Penfold; Edward H Wagner
Journal:  Gen Hosp Psychiatry       Date:  2015-02-28       Impact factor: 3.238

4.  End-of-life care discussions among patients with advanced cancer: a cohort study.

Authors:  Jennifer W Mack; Angel Cronin; Nathan Taback; Haiden A Huskamp; Nancy L Keating; Jennifer L Malin; Craig C Earle; Jane C Weeks
Journal:  Ann Intern Med       Date:  2012-02-07       Impact factor: 25.391

5.  Use of survivorship care plans in the United States: associations with survivorship care.

Authors:  Laura P Forsythe; Carla Parry; Catherine M Alfano; Erin E Kent; Corinne R Leach; David A Haggstrom; Patricia A Ganz; Noreen Aziz; Julia H Rowland
Journal:  J Natl Cancer Inst       Date:  2013-10-04       Impact factor: 13.506

6.  Did changes in drug reimbursement after the medicare modernization act affect chemotherapy prescribing?

Authors:  Mark C Hornbrook; Jennifer Malin; Jane C Weeks; Solomon B Makgoeng; Nancy L Keating; Arnold L Potosky
Journal:  J Clin Oncol       Date:  2014-09-29       Impact factor: 44.544

Review 7.  Palliative care and advance care planning for pancreas and other cancers.

Authors:  Rajiv Agarwal; Andrew S Epstein
Journal:  Chin Clin Oncol       Date:  2017-06

8.  The role of medical/nursing skills training in caregiver confidence and burden: A CanCORS study.

Authors:  Michelle A Mollica; Kristin Litzelman; Julia H Rowland; Erin E Kent
Journal:  Cancer       Date:  2017-07-20       Impact factor: 6.860

9.  Patients' expectations about effects of chemotherapy for advanced cancer.

Authors:  Jane C Weeks; Paul J Catalano; Angel Cronin; Matthew D Finkelman; Jennifer W Mack; Nancy L Keating; Deborah Schrag
Journal:  N Engl J Med       Date:  2012-10-25       Impact factor: 91.245

10.  How Does Caregiver Well-Being Relate to Perceived Quality of Care in Patients With Cancer? Exploring Associations and Pathways.

Authors:  Kristin Litzelman; Erin E Kent; Michelle Mollica; Julia H Rowland
Journal:  J Clin Oncol       Date:  2016-10-10       Impact factor: 44.544

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