Early recognition and management of chemotherapy toxicity is important in reducing
complications and contributes to improved quality of life and treatment compliance.
Typically, patients report treatment toxicity during pre-treatment visits but
they may also present as an emergency or unscheduled visit with acute symptoms.
Patient Reported Outcomes (PROs) have been proposed as a more efficient
method of collecting data on treatment toxicity (1-2), allowing more frequent and systematic monitoring
of symptoms.
Maguire et al developed the Daily Chemotherapy Toxicity self-Assessment Questionnaire (DCTAQ) as a novel PRO
to enable close monitoring of chemotherapy toxicity in clinical practice (3).
DCTAQ is an 11-item self-reported tool that assesses 10 core chemotherapy related symptoms
and item 11 invites patients to report any
other symptoms as free text .
Patients are asked to answer all questions based on
symptoms experienced in the past 24 hours.
The DCTAQ tool was developed based on an iterative process. Initially an expert and patient panel
reviewed a question pool to establish content validity. The tool was field-tested
in 82 patients with breast and colorectal cancer receiving adjuvant
chemotherapy across 8 hospital sites.
The tool was found to have modest
internal consistency and good test-retest reliability with Cohen’s Kappa
coefficient >0.8 across most items.
The DCTAQ tool was also used in a multi-centre randomised control trial (eSMART)
which investigated real-time monitoring of patient symptoms (4). Patients with
non-metastatic breast, colorectal cancer or lymphoma receiving curative intent
chemotherapy were randomised to an advanced symptom management system
(intervention group) or standard care. Patients in the intervention group reported
toxicity by completing the DCTAQ tool and also submitted their body temperature.
Symptoms reported using the DCTAQ tool were automatically evaluated and used to generate a colour coded alert to clinicians based on symptom urgency. The trial found that symptom burden, measured using the Memorial Symptom Assessment Scale was significantly lower in the intervention group compared to the standard care group.
Limitations of the DCTAQ tool are that it has only been tested in limited tumour
types, settings and a relatively small sample of patients.
References:
Howell D, Molloy S, Wilkinson K, et al. Patient-reported outcomes in routine cancer clinical practice: a scoping review of use, impact on health outcomes, and implementation factors. Ann Oncol Off J Eur Soc Med Oncol. 2015;26(9):1846-1858. doi:10.1093/annonc/mdv181
Absolom K, Warrington L, Hudson E, et al. Phase III Randomized Controlled Trial of eRAPID: eHealth Intervention During Chemotherapy. J Clin Oncol Off J Am Soc Clin Oncol. 2021;39(7):734-747. doi:10.1200/JCO.20.02015
Maguire R, Kotronoulas G, Donnan PT, et al. Development and preliminary testing of a brief clinical tool to enable daily monitoring of chemotherapy toxicity: The Daily Chemotherapy Toxicity self-Assessment Questionnaire. Eur J Cancer Care (Engl). 2018;27(6):e12890. doi:10.1111/ecc.12890
Maguire R, McCann L, Kotronoulas G, et al. Real time remote symptom monitoring during chemotherapy for cancer: European multicentre randomised controlled trial (eSMART). BMJ. 2021;374:n1647. doi:10.1136/bmj.n1647