Physicians may underestimate symptoms in breast cancer patients undergoing radiotherapy

07 Jan 2021 byRoshini Claire Anthony
Physicians may underestimate symptoms in breast cancer patients undergoing radiotherapy

Physicians may often underestimate symptoms of pain, oedema, fatigue, and pruritus in patients undergoing radiotherapy for breast cancer, according to a study presented at SABCS 2020.

Study participants were 13,725 patients enrolled in the Michigan Radiation Oncology Quality Consortium who underwent radiotherapy following lumpectomy between January 2012 and March 2020 at 29 centres in Michigan, US. Of these, 9,941 patients completed at least one patient-reported outcome (PRO) questionnaire during radiotherapy. Physician and patient ratings of symptoms of breast pain, oedema, fatigue, and pruritus were compared, with physician rating based on Common Terminology Criteria for Adverse Events (CTCAE). Under-recognition of symptoms was generally defined as physician rating of 0 (absent) when patients reported symptoms*.

About 24 percent of patients (n=2,363) reported frequent bother due to oedema, 24.9 percent (n=2,209) severe fatigue, 34.5 percent (n=3,434) substantial breast pain, and 30.6 percent (n=3,039) frequent bother from pruritus.

Under-recognition of symptoms was evaluated in 9,868 patients. Under-recognition was present in 30.9 percent of cases (n=2,094) of patient-reported moderate or severe pain, 36.7 percent (n=748) of patient-reported frequent pruritus, 51.4 percent (n=2,309) of patient-reported frequent oedema, and 18.8 percent (n=390) of patient-reported severe fatigue. [SABCS 2020, abstract GS3-07]

Among 5,510 patients who reported 1 of these symptoms during radiotherapy, 53.2 percent experienced at least one episode of under-recognition of 1 symptom. 

Compared with patients aged 60–69 years, those aged <50 and 50–59 years were at greater risk of under-recognition of symptoms (odds ratio [OR], 1.35, 95 percent confidence interval [CI], 1.15–1.58; p<0.001 and OR, 1.21, 95 percent CI, 1.06–1.39; p=0.006, respectively).

Black patients and those categorized as “other” race were more likely to have under-recognition of symptoms compared with White patients (OR, 1.92, 95 percent CI, 1.65–2.23; p<0.001 and OR, 1.82, 95 percent CI, 1.24–2.66; p=0.002, respectively). Asian patients had a numerically, but not significantly, increased risk of symptom under-recognition compared with White patients (OR, 1.32, 95 percent CI, 0.84–2.08; p=0.23).

Under-recognition of symptoms was also more common among patients who underwent conventional fractionation compared with hypofractionation (OR, 1.15, 95 percent CI, 1.02–1.30; p=0.02) and those treated at an academic vs a community facility (OR, 1.13, 95 percent CI, 1.01–1.27; p=0.04). Conversely, use of supraclavicular field was associated with a reduced likelihood of symptom under-recognition (OR, 0.80, 95 percent CI, 0.68–0.95; p=0.01).

“Recognizing side effects is necessary for physicians to provide supportive care to help patients manage their symptoms,” said study first author Professor Reshma Jagsi from the University of Michigan, Ann Arbor, Michigan, US.

“Physicians sometimes miscalculate the severity of patients’ symptoms, which can lead to reduced quality of life,” she continued. “[For instance,] it is possible that there is a misconception among medical professionals about the pain tolerance of patients based on age and race,” she said.

“Improving symptom detection is a potential way to reduce disparities in cancer treatment experiences and outcomes, at least in the setting of breast radiation therapy,” she pointed out.

Clinical trials depend on CTCAE which, according to the present findings, may miss out certain adverse events. As such, PROs may provide valuable information, said Jagsi and co-authors.

“Our study [has identified] some concerning patterns that need to be evaluated in future research, along with opportunities for intervention to improve the quality and equity of cancer care delivery,” Jagsi concluded.

 

 

*Under-recognition definition: Pain: Physician grade 0 when patients reported score of 4–6 (moderate) or physician grade 1 when patients reported score of 7–10 (severe); Pruritus and oedema: Physician grade 0 when patients reported bother often or all the time from itching or swelling; Fatigue: Physician grade 0 when patients reported significant fatigue most of the time or always