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Poster Display session 1

5568 - Assessing QUality of life and Experiences of diagnostic Trajectories of Sarcoma patients: The QUEST study protocol


28 Sep 2019


Poster Display session 1


Vicky Soomers


Annals of Oncology (2019) 30 (suppl_5): v683-v709. 10.1093/annonc/mdz283


V. Soomers1, O. Husson2, I.M.E. Desar1, D. Strauss3, R.L. Haas4, K. Verhoef5, M.A.J. van de Sande6, L. Been7, M.C. Parry8, L.V. van de Poll-Franse9, W.T. van der Graaf10

Author affiliations

  • 1 Medical Oncology, Radboud University Medical Center, 6525 GA - Nijmegen/NL
  • 2 Psychosocial Research And Epidemiology, Netherlands Cancer Institute/Antoni van Leeuwenhoek hospital (NKI-AVL), 1066 CX - Amsterdam/NL
  • 3 Sarcoma Unit, Royal Marsden Hospital NHS Foundation Trust, SW3 6JJ - London/GB
  • 4 Radiotherapy, The Netherlands Cancer Institute Antoni van Leeuwenhoek Hospital, 1066 CX - Amsterdam/NL
  • 5 Surgery, Erasmus University Medical Center, 3015 CE - Rotterdam/NL
  • 6 Orthopaedics, LUMC, 6525 GA - Leiden/NL
  • 7 Surgical Oncology, UMCG, 6525 GA - Groningen/NL
  • 8 Orthopaedics, Royal Orthopaedic Hospital NHS Foundation Trust, 6525 Ga - Birmingham/GB
  • 9 Epidemiology, Tilburg University, 6525 GA - Tilburg/NL
  • 10 Medical Oncology, Netherlands Cancer Institue - Antoni van Leeuwenhoek Hospital, Amsterdam/NL


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Abstract 5568


Sarcoma patients, like many other patients with rare diseases, often experience a long diagnostic trajectory, which may negatively affect their outcome in many ways. So far, research on diagnostic intervals has been retrospective. Prospective studies with large patient numbers comparing diagnostic intervals in different health care systems have not been performed. Moreover, next to survival, health-related quality of life (HRQoL) and patient satisfaction can be affected by experiencing diagnostic delay. Currently, no data are available on how the diagnostic trajectory impacts patient-reported outcomes among sarcoma patients.

Trial design

A longitudinal cohort study, QUEST, will be conducted among newly diagnosed sarcoma patients 18 years and older in one of the participating study centers in The Netherlands (five centers) or United Kingdom (3 centers). Patients will be invited before start of treatment and asked to complete questionnaires on the diagnostic pathway, risk factors (demographic, geographic, tumour characteristics etc) and patient-reported outcomes (HRQoL, social functioning, psychological distress, care satisfaction) at diagnosis and 3, 6, 12 and 24 months later. Data collection will be done within PROFILES, an established international registry for cancer patient reported outcomes. Clinical data, including vital status and tumour characteristics, will be collected from patients’ records. We aim to include 530 patients within two years, recruitment started 01-02-2018, and up till now 300patients completed baseline questionnaires (219 in NL, response rate 60%; 66 in UK, response rate 45%). Descriptive statistics will be used to quantify diagnostic intervals. The association between diagnostic interval and HRQoL, stage at diagnosis, primary treatment and survival will be explored.

Clinical trial identification

Protocol Record 2017-3881.

Editorial acknowledgement

Legal entity responsible for the study

Winette van der Graaf.


Radboudumc PROFILES registry.


All authors have declared no conflicts of interest.

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