Evidence map›Paper›PMID 37043710›Full record

ArticleJCO global oncology2023

Cancer Survivors' Experiences With and Preferences for Medical Information Disclosure and Advance Care Planning: An Online Survey Among Indonesian Cancer Support Groups.

Diah Martina, Rebecca Noerjani Angka, Rudi Putranto, Hamzah Shatri, Aru Wisaksono Sudoyo, Agnes van der Heide, Carin C D van der Rijt, Judith A C Rietjens

Abstract read
In one paragraph

Article in JCO global oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Key issues in palliative and supportive care research, policy and practice.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Diah MartinaDepartment of Medical Oncology, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, the Netherlands.ORCID 0000-0002-0889-223X
Rebecca Noerjani AngkaIndonesian Cancer Foundation Jakarta Chapter, Jakarta, Indonesia.
Rudi PutrantoDivision of Psychosomatic and Palliative Medicine, Department of Internal Medicine, Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia.
Hamzah ShatriDivision of Psychosomatic and Palliative Medicine, Department of Internal Medicine, Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia.
Aru Wisaksono SudoyoCipto Mangunkusumo National General Hospital, Jakarta, Indonesia.ORCID 0000-0002-4827-9392
Agnes van der HeideDepartment of Public Health, Erasmus MC, University Medical Centre Rotterdam, the Netherlands.ORCID 0000-0001-5584-4305
Carin C D van der RijtDepartment of Medical Oncology, Erasmus MC Cancer Institute, University Medical Centre Rotterdam, the Netherlands.
Judith A C RietjensDepartment of Public Health, Erasmus MC, University Medical Centre Rotterdam, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo understand the experiences and preferences of Indonesian cancer survivors regarding medical information disclosure and advance care planning.

methodsOn the basis of systematic reviews of the scientific literature, qualitative studies, and expert-panel input, we developed an online survey that was distributed to nine cancer survivor support groups in Indonesia.

resultsA total of 1,030 valid responses were received. Most participants were younger than 60 years (92%), female (91%), married (78%), Muslim (75%), diagnosed with breast cancer (68%), highly educated (64%), and more than one year beyond diagnosis of their cancer. If diagnosed with a life-limiting illness, participants wished to be informed about their diagnosis (74%), disease severity (61%), estimated curability (81%), expected disease trajectory (66%), and estimated life expectancy (37%). Between 46%-69% of the participants wished to discuss four topics of advance care planning (end-of-life treatments, resuscitation, health care proxies, and what matters at the end of life); 21%-42% had done so. Of those who wished to discuss these topics, 36%-79% preferred to do so with their family members. The most important reasons for not being willing to engage in advance care planning were the desire to surrender to God's will and to focus on here and now.

conclusionIn a group of cancer survivors, most of them were highly educated, young, female, and diagnosed with breast cancer. Their preferences for medical information and advance care planning varied, with the majority wishing for information and involvement in advance care planning. Culturally sensitive advance care planning involves health care professionals eliciting individuals' preferences for medical information disclosure and discussing different topics in advance care planning conversations.

Indexed as

Advance Care PlanningBreast NeoplasmsCancer SurvivorsDisclosureFemaleHumansIndonesiaSystematic Reviews as Topic

Identifiers

PMID37043710
PMCPMC10281438

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.