Journal of Clinical Oncology, Vol 22, No 9 (May 1), 2004: pp. 1721-1730
© 2004 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2004.04.095
Cancer Patient Preferences for Communication of Prognosis in the Metastatic Setting
Rebecca G. Hagerty,
Phyllis N. Butow,
Peter A. Ellis,
Elizabeth A. Lobb,
Susan Pendlebury,
Natasha Leighl,
David Goldstein,
Sing Kai Lo,
Martin H.N. Tattersall
From the Medical Psychology Research Unit and the Department of Cancer Medicine, University of Sydney, Sydney; and Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Address reprint requests to Phyllis Butow, PhD, Medical Psychology Research Unit, Blackburn Building, D06, University of Sydney, Sydney, NSW 2006, Australia; e-mail: phyllisb{at}med.usyd.edu.au
PURPOSE: To identify preferences for and predictors of prognostic information among patients with incurable metastatic cancer.
PATIENTS AND METHODS: One hundred twenty-six metastatic cancer patients seeing 30 oncologists at 12 outpatient clinics in New South Wales, Australia, participated in the study. Patients were diagnosed with incurable metastatic disease within 6 weeks to 6 months of recruitment. Patients completed a survey eliciting their preferences for prognostic information, including type, quantity, mode, and timing of presentation; anxiety and depression levels; and information and involvement preferences.
RESULTS: More than 95% of patients wanted information about side effects, symptoms, and treatment options. The majority wanted to know longest survival time with treatment (85%), 5-year survival rates (80%), and average survival (81%). Words and numbers were preferred over pie charts or graphs. Fifty-nine percent (59%) wanted to discuss expected survival when first diagnosed with metastatic disease. Thirty-eight percent and 44% wanted to negotiate when expected survival and dying, respectively, were discussed. Patients with higher depression scores were more likely to want to know shortest time to live without treatment (P = .047) and average survival (P = .049). Lower depression levels were significantly associated with never wanting to discuss expected survival (P = .03). Patients with an expected survival of years were more likely to want to discuss life expectancy when first diagnosed with metastases (P = .02).
CONCLUSION: Most metastatic cancer patients want detailed prognostic information but prefer to negotiate the extent, format, and timing of the information they receive from their oncologists.
Supported by the New South Wales Cancer Council.
Presented at the 29th Annual Scientific Meeting of the Clinical Oncological Society of Australia, Sydney, 2002.
Authors' disclosures of potential conflicts of interest are found at the end of this article.
This article has been cited by other articles:

|
 |

|
 |
 
A B Astrow, J R Sood, M T Nolan, P B Terry, L Clawson, J Kub, M Hughes, and D P Sulmasy
Decision-making in patients with advanced cancer compared with amyotrophic lateral sclerosis
J. Med. Ethics,
September 1, 2008;
34(9):
664 - 668.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F. Twomey, N. O'Leary, and T. O'Brien
Prediction of Patient Survival by Healthcare Professionals in a Specialist Palliative Care Inpatient Unit: A Prospective Study
American Journal of Hospice and Palliative Medicine,
May 1, 2008;
25(2):
139 - 145.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Gabrijel, L. Grize, E. Helfenstein, M. Brutsche, P. Grossman, M. Tamm, and A. Kiss
Receiving the Diagnosis of Lung Cancer: Patient Recall of Information and Satisfaction With Physician Communication
J. Clin. Oncol.,
January 10, 2008;
26(2):
297 - 302.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. L. Back, R. M. Arnold, and J. A. Tulsky
Discussing Prognosis
ASCO Educational Book,
January 1, 2008;
2008(1):
135 - 138.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F. Efficace, A. Novik, M. Vignetti, F. Mandelli, and C. S. Cleeland
Health-related quality of life and symptom assessment in clinical research of patients with hematologic malignancies: where are we now and where do we go from here?
Haematologica,
December 1, 2007;
92(12):
1596 - 1598.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M Sanjo, M Miyashita, T Morita, K Hirai, M Kawa, T Akechi, and Y Uchitomi
Preferences regarding end-of-life cancer care and associations with good-death concepts: a population-based survey in Japan
Ann. Onc.,
September 1, 2007;
18(9):
1539 - 1547.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Buckman and W. Baile
Truth Telling: Yes, but How?
J. Clin. Oncol.,
July 20, 2007;
25(21):
3181 - 3181.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. W. Mack, E. F. Cook, J. Wolfe, H. E. Grier, P. D. Cleary, and J. C. Weeks
Understanding of Prognosis Among Parents of Children With Cancer: Parental Optimism and the Parent-Physician Interaction
J. Clin. Oncol.,
April 10, 2007;
25(11):
1357 - 1362.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F Efficace, D Osoba, C Gotay, M Sprangers, C Coens, and A Bottomley
Has the quality of health-related quality of life reporting in cancer clinical trials improved over time? Towards bridging the gap with clinical decision making
Ann. Onc.,
April 1, 2007;
18(4):
775 - 781.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G Oskay-Ozcelik, W Lehmacher, D Konsgen, H Christ, M Kaufmann, W Lichtenegger, M Bamberg, D Wallwiener, F Overkamp, K Diedrich, et al.
Breast cancer patients' expectations in respect of the physician-patient relationship and treatment management results of a survey of 617 patients
Ann. Onc.,
March 1, 2007;
18(3):
479 - 484.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. W. Mack, J. Wolfe, H. E. Grier, P. D. Cleary, and J. C. Weeks
Communication About Prognosis Between Parents and Physicians of Children With Cancer: Parent Preferences and the Impact of Prognostic Information
J. Clin. Oncol.,
November 20, 2006;
24(33):
5265 - 5270.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. Schofield, M. Carey, A. Love, C. Nehill, and S. Wein
'Would you like to talk about your future treatment options?' discussing the transition from curative cancer treatment to palliative care
Palliative Medicine,
June 1, 2006;
20(4):
397 - 406.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Iconomou, A. Viha, A. Koutras, I. Koukourikou, V. Mega, T. Makatsoris, A. Onyenadum, K. Assimakopoulos, A. G. Vagenakis, and H. P. Kalofonos
Impact of providing booklets about chemotherapy to newly presenting patients with cancer: a randomized controlled trial
Ann. Onc.,
March 1, 2006;
17(3):
515 - 520.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. T. Keating, K. Nayeem, J.J. Gilmartin, and S. T. O'Keeffe
Advance Directives for Truth Disclosure
Chest,
August 1, 2005;
128(2):
1037 - 1039.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. R. Helft
Necessary Collusion: Prognostic Communication With Advanced Cancer Patients
J. Clin. Oncol.,
May 1, 2005;
23(13):
3146 - 3150.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. G. Hagerty, P. N. Butow, P. M. Ellis, E. A. Lobb, S. C. Pendlebury, N. Leighl, C. Mac Leod, and M. H.N. Tattersall
Communicating With Realism and Hope: Incurable Cancer Patients' Views on the Disclosure of Prognosis
J. Clin. Oncol.,
February 20, 2005;
23(6):
1278 - 1288.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|