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Survivorship and the chronic cancer patient: Patterns in treatment-related effects, follow-up care, and use of survivorship care plans.
Frick, Melissa A; Vachani, Carolyn C; Bach, Christina; Hampshire, Margaret K; Arnold-Korzeniowski, Karen; Metz, James M; Hill-Kayser, Christine E.
Affiliation
  • Frick MA; Department of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Vachani CC; Department of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Bach C; Department of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Hampshire MK; Department of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Arnold-Korzeniowski K; Department of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Metz JM; Department of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Hill-Kayser CE; Department of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.
Cancer ; 123(21): 4268-4276, 2017 Nov 01.
Article in En | MEDLINE | ID: mdl-28654153
ABSTRACT

BACKGROUND:

The survivorship needs of patients living with chronic cancer (CC) and their use of survivorship care plans (SCPs) have been overlooked and underappreciated.

METHODS:

A convenience sample of 39,088 SCPs completed for cancer survivors with an Internet-based SCP tool was examined; it included 5847 CC survivors (15%; CC was defined as chronic leukemia and/or recurrent/metastatic cancer of another nature). Patient-reported treatment effects and follow-up care patterns were compared between CC survivors and survivors treated with curative intent (CI). Responses from a follow-up survey regarding SCP satisfaction and use were reviewed.

RESULTS:

CC survivors had greater odds of experiencing multiple treatment-related effects than survivors treated with CI; these effects included fatigue, cognitive changes, dyspnea, peripheral neuropathy, lymphedema, and erectile dysfunction. Nearly half of CC survivors were managed by an oncologist alone, and they were less likely than CI patients to be comanaged by a primary care provider and an oncologist. Fewer SCPs were generated by health care providers (HCPs) for CC survivors versus CI survivors. A smaller proportion of CC users versus CI users rated their experience and satisfaction with the SCP tool as very good or excellent, and CC users were less likely to share the HCP summary with their health care team.

CONCLUSIONS:

A substantial number of CC survivors, often considered incurable but treatable, seek survivorship support. Tools to facilitate participation, communication, and coordination of care are valuable for these patients, and future iterations of SCPs should be designed to address the particular circumstances of living with CC. Cancer 2017;1234268-4276. © 2017 American Cancer Society.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Survivors / Continuity of Patient Care / Needs Assessment / Neoplasm Recurrence, Local / Neoplasms Aspects: Patient_preference Limits: Female / Humans / Male / Middle aged Language: En Journal: Cancer Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Survivors / Continuity of Patient Care / Needs Assessment / Neoplasm Recurrence, Local / Neoplasms Aspects: Patient_preference Limits: Female / Humans / Male / Middle aged Language: En Journal: Cancer Year: 2017 Document type: Article