Pain in patients with newly diagnosed or relapsed acute leukemia.
Acute Disease
Adolescent
Adult
Age of Onset
Aged
Aged, 80 and over
Cancer Pain
/ diagnosis
Female
Humans
Leukemia
/ complications
Leukemia, Myeloid, Acute
/ complications
Male
Middle Aged
Pain
/ diagnosis
Pain Measurement
Precursor Cell Lymphoblastic Leukemia-Lymphoma
/ complications
Prevalence
Recurrence
Young Adult
Acute leukemia
Cancer
Hematology
Oncology
Pain
Journal
Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957
Informations de publication
Date de publication:
Aug 2019
Aug 2019
Historique:
received:
16
09
2018
accepted:
28
11
2018
pubmed:
12
12
2018
medline:
3
9
2019
entrez:
12
12
2018
Statut:
ppublish
Résumé
Acute leukemia (AL) is associated with substantial morbidity and mortality. We assessed the prevalence and correlates of pain in patients with newly diagnosed or relapsed AL. Patients with newly diagnosed or relapsed AL admitted to a comprehensive cancer center completed the Memorial Symptom Assessment Scale (MSAS), which assesses prevalence, severity, and distress associated with pain and other symptoms. Factors associated with severe pain were assessed using logistic regression. Two raters completed chart reviews in duplicate for patients with severe pain (MSAS severity ≥ 3/4) to determine the site of pain. Three hundred eighteen patients were recruited from January 2008 to October 2013: 245 (77.0%) had acute myeloid or acute promyelocytic leukemia (AML/APL) and 73 (23.0%) had acute lymphoblastic leukemia (ALL); 289 (90.9%) were newly diagnosed and 29 (9.1%) had relapsed disease. Pain was reported in 156/318 (49.2%), of whom 55/156 (35.3%) reported severe pain (≥ 3/4). Pain was associated with all psychological symptoms (all p < 0.005) and some physical symptoms. Severe pain was associated with younger age (p = 0.02), worse performance status (p = 0.04), ALL diagnosis (p = 0.04), and time from onset of chemotherapy (p = 0.03), with pain peaking at 4 weeks after chemotherapy initiation. The most common sites of severe pain were oropharynx (22; 40%), head (12; 21.8%), and abdomen (11; 20%). Only 3 patients (0.9%) were referred to the symptom control/palliative care team during the month prior to or following assessment. Pain is frequent, distressing, and predictable in patients undergoing induction chemotherapy for AL. Further research is needed to assess the efficacy of early supportive care in this population.
Identifiants
pubmed: 30535882
doi: 10.1007/s00520-018-4583-5
pii: 10.1007/s00520-018-4583-5
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2789-2797Subventions
Organisme : Canadian Institutes of Health Research
ID : 84317
Pays : Canada
Organisme : Canadian Cancer Society
ID : 702603
Organisme : Princess Margaret Cancer Foundation
ID : NA
Organisme : Ontario Ministry of Health and Long-Term Care
ID : NA