Skip to main content
Top
Published in: BMC Palliative Care 1/2021

Open Access 01-12-2021 | Research article

Communication of Pharmacogenomic test results and treatment plans in pediatric oncology: deliberative stakeholder consultations with parents

Authors: Cristina Longo, Vasiliki Rahimzadeh, Gillian Bartlett

Published in: BMC Palliative Care | Issue 1/2021

Login to get access

Abstract

Background

Effective communication in support of clinical decision-making is central to the pediatric cancer care experience for families. A new laboratory derived pharmacogenetic test (LDT) that can diagnose difficult-to-treat brain cancers has been developed to stratify children based on their ability to respond to available treatment; however, the potential implementation of the LDT may make effective communication challenging since it can potentially remove the option for curative treatment in those children identified as non-responders, i.e. those with a catastrophic diagnosis.

Objective

We solicited the perspectives of parents of children with difficult-to-treat brain cancer on communication preferences surrounding the potential implementation of the LDT in standard care using deliberative stakeholder consultations.

Methods

Eight bereaved parents of children who succumbed to difficult-to-treat brain cancer, and four parents of children currently undergoing treatment for similar cancers attended separate small-group deliberative consultations – a stakeholder engagement method that enables the co-creation of recommendations following the consideration of competing arguments and diverse opinions of parents with different experiences. In the small-group consultations (Phase I), parents discussed four questions about potential communication issues that may arise with the LDT in practice. In Phase II, a total of five parents from both stakeholder groups (4 bereaved and 1 in current treatment) attended a consultation, known as the ‘mixed’ consultation, with the purpose of co-developing concrete recommendations for implementation of the LDT.

Results

Explaining the risks, benefits, and accuracy of the LDT were considered essential to parents. Once an LDT-based diagnosis/prognosis can be made, parents valued honesty, empathy, and clarity in communication. Parents also requested that all results and treatment options be presented to them in measured doses, and in an unbiased manner over the course of several meetings. This communication strategy allowed sufficient time to understand and accept the diagnosis/prognosis, particularly if it was catastrophic. Continuous access to the appropriate psychological and social support or counselling at and post-diagnosis was also strongly recommended.

Conclusions

Deliberants co-created family-centered recommendations surrounding communication issues of the LDT, providing guidance to pediatric oncologists that could implement the test in practice.
Appendix
Available only for authorised users
Literature
1.
go back to reference Dobrozsi S, Trowbridge A, Mack JW, Rosenberg AR. Effective communication for newly diagnosed pediatric patients with Cancer: considerations for the patients, family members, providers, and multidisciplinary team. Am Soc Clin Oncol Educ Book. 2019;39:573–81.CrossRef Dobrozsi S, Trowbridge A, Mack JW, Rosenberg AR. Effective communication for newly diagnosed pediatric patients with Cancer: considerations for the patients, family members, providers, and multidisciplinary team. Am Soc Clin Oncol Educ Book. 2019;39:573–81.CrossRef
2.
go back to reference Odeniyi F, Nathanson PG, Schall TE, Walter JK. Communication challenges of oncologists and Intensivists caring for pediatric oncology patients: a qualitative study. J Pain Symptom Manag. 2017;54(6):909–15.CrossRef Odeniyi F, Nathanson PG, Schall TE, Walter JK. Communication challenges of oncologists and Intensivists caring for pediatric oncology patients: a qualitative study. J Pain Symptom Manag. 2017;54(6):909–15.CrossRef
3.
go back to reference Mack JW, Wolfe J, Grier HE, Cleary PD, Weeks JC. Communication about prognosis between parents and physicians of children with cancer: parent preferences and the impact of prognostic information. J Clin Oncol. 2006;24(33):5265–70.CrossRef Mack JW, Wolfe J, Grier HE, Cleary PD, Weeks JC. Communication about prognosis between parents and physicians of children with cancer: parent preferences and the impact of prognostic information. J Clin Oncol. 2006;24(33):5265–70.CrossRef
4.
go back to reference Marron JM, Cronin AM, Kang TI, Mack JW. Intended and unintended consequences: ethics, communication, and prognostic disclosure in pediatric oncology. Cancer. 2018;124(6):1232–41.CrossRef Marron JM, Cronin AM, Kang TI, Mack JW. Intended and unintended consequences: ethics, communication, and prognostic disclosure in pediatric oncology. Cancer. 2018;124(6):1232–41.CrossRef
5.
go back to reference Karremann M, Gielen GH, Hoffmann M, Wiese M, Colditz N, Warmuth-Metz M, Bison B, Claviez A, van Vuurden DG, von Bueren AO, et al. Diffuse high-grade gliomas with H3 K27M mutations carry a dismal prognosis independent of tumor location. Neuro-Oncology. 2018;20(1):123–31.CrossRef Karremann M, Gielen GH, Hoffmann M, Wiese M, Colditz N, Warmuth-Metz M, Bison B, Claviez A, van Vuurden DG, von Bueren AO, et al. Diffuse high-grade gliomas with H3 K27M mutations carry a dismal prognosis independent of tumor location. Neuro-Oncology. 2018;20(1):123–31.CrossRef
6.
go back to reference Khuong-Quang DA, Buczkowicz P, Rakopoulos P, Liu XY, Fontebasso AM, Bouffet E, Bartels U, Albrecht S, Schwartzentruber J, Letourneau L, et al. K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas. Acta Neuropathol. 2012;124(3):439–47.CrossRef Khuong-Quang DA, Buczkowicz P, Rakopoulos P, Liu XY, Fontebasso AM, Bouffet E, Bartels U, Albrecht S, Schwartzentruber J, Letourneau L, et al. K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas. Acta Neuropathol. 2012;124(3):439–47.CrossRef
7.
go back to reference Davies B, Sehring SA, Partridge JC, Cooper BA, Hughes A, Philp JC, Amidi-Nouri A, Kramer RF. Barriers to palliative care for children: perceptions of pediatric health care providers. Pediatrics. 2008;121(2):282–8.CrossRef Davies B, Sehring SA, Partridge JC, Cooper BA, Hughes A, Philp JC, Amidi-Nouri A, Kramer RF. Barriers to palliative care for children: perceptions of pediatric health care providers. Pediatrics. 2008;121(2):282–8.CrossRef
8.
go back to reference Wolfe J, Klar N, Grier HE, Duncan J, Salem-Schatz S, Emanuel EJ, Weeks JC. Understanding of prognosis among parents of children who died of cancer - impact on treatment goals and integration of palliative care. JAMA. 2000;284(19):2469–75.CrossRef Wolfe J, Klar N, Grier HE, Duncan J, Salem-Schatz S, Emanuel EJ, Weeks JC. Understanding of prognosis among parents of children who died of cancer - impact on treatment goals and integration of palliative care. JAMA. 2000;284(19):2469–75.CrossRef
9.
go back to reference Bartlett G, Longo C, Puzhko S, Gagnon J, Rahimzadeh V. Deliberative stakeholder consultations: creating insights into effective practice-change in family medicine. Fam Pract. 2018;35(6):749–52.CrossRef Bartlett G, Longo C, Puzhko S, Gagnon J, Rahimzadeh V. Deliberative stakeholder consultations: creating insights into effective practice-change in family medicine. Fam Pract. 2018;35(6):749–52.CrossRef
10.
go back to reference Longo C, Rahimzadeh V, O'Doherty K, Bartlett G. Addressing ethical challenges at the intersection of pharmacogenomics and primary care using deliberative consultations. Pharmacogenomics. 2016;17(16):1795–805.CrossRef Longo C, Rahimzadeh V, O'Doherty K, Bartlett G. Addressing ethical challenges at the intersection of pharmacogenomics and primary care using deliberative consultations. Pharmacogenomics. 2016;17(16):1795–805.CrossRef
11.
go back to reference Doria N, Condran B, Boulos L. Sharpening the focus: differentiating between focus groups for patient engagement versus qualitative research. Int J Qual Methods. 2018;17(1):7–7. Doria N, Condran B, Boulos L. Sharpening the focus: differentiating between focus groups for patient engagement versus qualitative research. Int J Qual Methods. 2018;17(1):7–7.
13.
go back to reference De Vries R, Stanczyk AE, Ryan KA, Kim SYH. A framework for assessing the quality of democratic deliberation: enhancing deliberation as a tool for bioethics. J Empir Res Hum Res. 2011;6(3):3–17.CrossRef De Vries R, Stanczyk AE, Ryan KA, Kim SYH. A framework for assessing the quality of democratic deliberation: enhancing deliberation as a tool for bioethics. J Empir Res Hum Res. 2011;6(3):3–17.CrossRef
14.
go back to reference Sisk BA, Mack JW, Ashworth R, et al. Communication in pediatric oncology: State of the field and research agenda. Pediatr Blood Cancer. 2018;65:e26727. Sisk BA, Mack JW, Ashworth R, et al. Communication in pediatric oncology: State of the field and research agenda. Pediatr Blood Cancer. 2018;65:e26727.
15.
go back to reference Zwaanswijk M, Tates K, van Dulmen S, Hoogerbrugge PM, Kamps WA, Bensing JM. Young patients', parents', and survivors' communication preferences in paediatric oncology: results of online focus groups. BMC Pediatr. 2007;7:35.CrossRef Zwaanswijk M, Tates K, van Dulmen S, Hoogerbrugge PM, Kamps WA, Bensing JM. Young patients', parents', and survivors' communication preferences in paediatric oncology: results of online focus groups. BMC Pediatr. 2007;7:35.CrossRef
16.
go back to reference Snaman JM, Torres C, Duffy B, Levine DR, Gibson DV, Baker JN. Parental perspectives of communication at the end of life at a pediatric oncology institution. J Palliat Med. 2016;19(3):326–32.CrossRef Snaman JM, Torres C, Duffy B, Levine DR, Gibson DV, Baker JN. Parental perspectives of communication at the end of life at a pediatric oncology institution. J Palliat Med. 2016;19(3):326–32.CrossRef
17.
go back to reference Johnson LM, Leek AC, Drotar D, Noll RB, Rheingold SR, Kodish ED, Baker JN. Practical communication guidance to improve phase 1 informed consent conversations and decision-making in pediatric oncology. Cancer. 2015;121(14):2439–48.CrossRef Johnson LM, Leek AC, Drotar D, Noll RB, Rheingold SR, Kodish ED, Baker JN. Practical communication guidance to improve phase 1 informed consent conversations and decision-making in pediatric oncology. Cancer. 2015;121(14):2439–48.CrossRef
18.
go back to reference von Essen L, Enskar K, Skolin I. Important aspects of care and assistance for parents of children, 0-18 years of age, on or off treatment for cancer. Parent and nurse perceptions. Eur J Oncol Nurs. 2001;5(4):254–64.CrossRef von Essen L, Enskar K, Skolin I. Important aspects of care and assistance for parents of children, 0-18 years of age, on or off treatment for cancer. Parent and nurse perceptions. Eur J Oncol Nurs. 2001;5(4):254–64.CrossRef
19.
go back to reference Clarke JN, Fletcher P. Communication issues faced by parents who have a child diagnosed with Cancer. J Pediatr Oncol Nurs. 2003;20(4):175–91.CrossRef Clarke JN, Fletcher P. Communication issues faced by parents who have a child diagnosed with Cancer. J Pediatr Oncol Nurs. 2003;20(4):175–91.CrossRef
20.
go back to reference Baker JN, Leek AC, Salas HS, Drotar D, Noll R, Rheingold SR, Kodish ED. Suggestions from adolescents, young adults, and parents for improving informed consent in phase 1 pediatric oncology trials. Cancer. 2013;119(23):4154–61.CrossRef Baker JN, Leek AC, Salas HS, Drotar D, Noll R, Rheingold SR, Kodish ED. Suggestions from adolescents, young adults, and parents for improving informed consent in phase 1 pediatric oncology trials. Cancer. 2013;119(23):4154–61.CrossRef
21.
go back to reference Hinds PS, Drew D, Oakes LL, Fouladi M, Spunt SL, Church C, Furman WL. End-of-life care preferences of pediatric patients with cancer. J Clin Oncol. 2005;23(36):9146–54.CrossRef Hinds PS, Drew D, Oakes LL, Fouladi M, Spunt SL, Church C, Furman WL. End-of-life care preferences of pediatric patients with cancer. J Clin Oncol. 2005;23(36):9146–54.CrossRef
22.
go back to reference Jackson AC, Stewart H, O'Toole M, Tokatlian N, Enderby K, Miller J, Ashley D. Pediatric brain tumor patients: their parents' perceptions of the hospital experience. J Pediatr Oncol Nurs. 2007;24(2):95–105.CrossRef Jackson AC, Stewart H, O'Toole M, Tokatlian N, Enderby K, Miller J, Ashley D. Pediatric brain tumor patients: their parents' perceptions of the hospital experience. J Pediatr Oncol Nurs. 2007;24(2):95–105.CrossRef
23.
go back to reference Kastel A, Enskar K, Bjork O. Parents' views on information in childhood cancer care. Eur J Oncol Nurs. 2011;15(4):290–5.CrossRef Kastel A, Enskar K, Bjork O. Parents' views on information in childhood cancer care. Eur J Oncol Nurs. 2011;15(4):290–5.CrossRef
24.
go back to reference Kessel RM, Roth M, Moody K, Levy A. Day one talk: parent preferences when learning that their child has cancer. Support Care Cancer. 2013;21(11):2977–82.CrossRef Kessel RM, Roth M, Moody K, Levy A. Day one talk: parent preferences when learning that their child has cancer. Support Care Cancer. 2013;21(11):2977–82.CrossRef
25.
go back to reference Kilicarslan-Toruner E, Akgun-Citak E. Information-seeking behaviours and decision-making process of parents of children with cancer. Eur J Oncol Nurs. 2013;17(2):176–83.CrossRef Kilicarslan-Toruner E, Akgun-Citak E. Information-seeking behaviours and decision-making process of parents of children with cancer. Eur J Oncol Nurs. 2013;17(2):176–83.CrossRef
26.
go back to reference Parker TA, Johnston DL. Parental perceptions of being told their child has cancer. Pediatr Blood Cancer. 2008;51(4):531–4.CrossRef Parker TA, Johnston DL. Parental perceptions of being told their child has cancer. Pediatr Blood Cancer. 2008;51(4):531–4.CrossRef
27.
go back to reference Young B, Dixon-Woods M, Windridge KC, Heney D. Managing communication with young people who have a potentially life threatening chronic illness: qualitative study of patients and parents. Brit Med J. 2003;326(7384):305–308b.CrossRef Young B, Dixon-Woods M, Windridge KC, Heney D. Managing communication with young people who have a potentially life threatening chronic illness: qualitative study of patients and parents. Brit Med J. 2003;326(7384):305–308b.CrossRef
28.
go back to reference Zwaanswijk M, Tates K, van Dulmen S, Hoogerbrugge PM, Kamps WA, Beishuizen A, Bensing JM. Communicating with child patients in pediatric oncology consultations: a vignette study on child patients', parents', and survivors' communication preferences. Psychooncology. 2011;20(3):269–77.CrossRef Zwaanswijk M, Tates K, van Dulmen S, Hoogerbrugge PM, Kamps WA, Beishuizen A, Bensing JM. Communicating with child patients in pediatric oncology consultations: a vignette study on child patients', parents', and survivors' communication preferences. Psychooncology. 2011;20(3):269–77.CrossRef
29.
go back to reference Young B, Ward J, Salmon P, Gravenhorst K, Hill J, Eden T. Parents' experiences of their Children's presence in discussions with physicians about leukemia. Pediatrics. 2011;127(5):E1230–8.CrossRef Young B, Ward J, Salmon P, Gravenhorst K, Hill J, Eden T. Parents' experiences of their Children's presence in discussions with physicians about leukemia. Pediatrics. 2011;127(5):E1230–8.CrossRef
30.
go back to reference Orioles A, Miller VA, Kersun LS, Ingram M, Morrison WE. "To be a phenomenal doctor you have to be the whole package": Physicians' interpersonal behaviors during difficult conversations in pediatrics. J Palliat Med. 2013;16(8):929–33.CrossRef Orioles A, Miller VA, Kersun LS, Ingram M, Morrison WE. "To be a phenomenal doctor you have to be the whole package": Physicians' interpersonal behaviors during difficult conversations in pediatrics. J Palliat Med. 2013;16(8):929–33.CrossRef
31.
go back to reference Johnston DL, Nagel K, Friedman DL, Meza JL, Hurwitz CA, Friebert S. Availability and use of palliative care and end-of-life services for pediatric oncology patients. J Clin Oncol. 2008;26(28):4646–50.CrossRef Johnston DL, Nagel K, Friedman DL, Meza JL, Hurwitz CA, Friebert S. Availability and use of palliative care and end-of-life services for pediatric oncology patients. J Clin Oncol. 2008;26(28):4646–50.CrossRef
32.
go back to reference Hazen RA, Zyzanski S, Baker JN, Drotar D, Kodish E. Communication about the risks and benefits of phase I pediatric oncology trials. Contemp Clin Trials. 2015;41:139–45.CrossRef Hazen RA, Zyzanski S, Baker JN, Drotar D, Kodish E. Communication about the risks and benefits of phase I pediatric oncology trials. Contemp Clin Trials. 2015;41:139–45.CrossRef
Metadata
Title
Communication of Pharmacogenomic test results and treatment plans in pediatric oncology: deliberative stakeholder consultations with parents
Authors
Cristina Longo
Vasiliki Rahimzadeh
Gillian Bartlett
Publication date
01-12-2021
Publisher
BioMed Central
Published in
BMC Palliative Care / Issue 1/2021
Electronic ISSN: 1472-684X
DOI
https://doi.org/10.1186/s12904-021-00709-2

Other articles of this Issue 1/2021

BMC Palliative Care 1/2021 Go to the issue