Skip to main content
Top
Published in: Breast Cancer Research and Treatment 3/2017

01-12-2017 | Clinical trial

Lymphedema, musculoskeletal events and arm function in older patients receiving adjuvant chemotherapy for breast cancer (Alliance A171302)

Authors: Judith O. Hopkins, Jake Allred, Arti Hurria, Aminah Jatoi, Jacqueline M. Lafky, Harvey Cohen, Clifford Hudis, Eric Winer, Jeanne Mandelblatt, Ann Partridge, Lisa Carey, Hyman B. Muss

Published in: Breast Cancer Research and Treatment | Issue 3/2017

Login to get access

Abstract

Purpose

Musculoskeletal events (MEs) resulting from breast cancer treatment can significantly interfere with the quality of life (QOL) of older adults. We evaluated the incidence of MEs in women 65 years and older who had surgery and adjuvant chemotherapy for breast cancer, and the impact of treatment on MEs and arm function.

Patients and methods

Patient-reported data in Alliance/CALGB 49907 were collected using the EORTC QLQ-BR23 and physician-reported adverse events to characterize self-reported MEs and incidence of lymphedema. EORTC QLQ-BR23 items related to musculoskeletal events were analyzed in this study and data collected at study entry (post-operative) and 12 and 24 months post-entry.

Results

Lymphedema, arm function, and ME data were available for 321 patients. One or more MEs were reported by 87% (median number = 3) and 64% (median number = 1) of patients post-operatively and at 24 months. At 24 months 2% had persistence of six MEs. Seventy-four percent experienced at least ≥3/6 types of MEs over the 24-month period. Detection of lymphedema at any time during the study was noted in 7.5% of the patients and appeared to be associated with the type of chemotherapy given: CMF 16.4%, capecitabine 5.8%, and AC 4%. Mastectomy and axillary node dissection were associated with the most MEs. LROM correlated with poorer arm function at all time periods.

Conclusion

Potentially debilitating MEs occur in three-fourths of elderly women undergoing standard therapy for breast cancer. Emphasis should be placed on prevention, identification, and treatment of these MEs to improve QOL.
Appendix
Available only for authorised users
Literature
1.
go back to reference Shah C, Arthur D, Riutta J et al (2012) Breast-cancer related lymphedema: a review of procedure-specific incidence rates, clinical assessment AIDS, treatment paradigms, and risk reduction. Breast J 18:357–361CrossRefPubMed Shah C, Arthur D, Riutta J et al (2012) Breast-cancer related lymphedema: a review of procedure-specific incidence rates, clinical assessment AIDS, treatment paradigms, and risk reduction. Breast J 18:357–361CrossRefPubMed
2.
go back to reference Ozcinar B, Guler SA, Kocaman N et al (2012) Breast cancer related lymphedema in patients with different loco-regional treatments. Breast 21:361–365CrossRefPubMed Ozcinar B, Guler SA, Kocaman N et al (2012) Breast cancer related lymphedema in patients with different loco-regional treatments. Breast 21:361–365CrossRefPubMed
3.
go back to reference Kwan W, Jackson J, Weir LM et al (2002) Chronic arm morbidity after curative breast cancer treatment: prevalence and impact on quality of life. J Clin Oncol 20:4242–4248CrossRefPubMed Kwan W, Jackson J, Weir LM et al (2002) Chronic arm morbidity after curative breast cancer treatment: prevalence and impact on quality of life. J Clin Oncol 20:4242–4248CrossRefPubMed
4.
go back to reference Tasmuth T, von Smitten K, Kalso E (1996) Pain and other symptoms during the first year after radical and conservative surgery for breast cancer. Br J Cancer 74:2024–2031CrossRefPubMedPubMedCentral Tasmuth T, von Smitten K, Kalso E (1996) Pain and other symptoms during the first year after radical and conservative surgery for breast cancer. Br J Cancer 74:2024–2031CrossRefPubMedPubMedCentral
5.
go back to reference Miaskowski C, Cooper B, Paul SM et al (2012) Identification of patient subgroups and risk factors for persistent breast pain following breast cancer surgery. J Pain 13:1172–1187CrossRefPubMedPubMedCentral Miaskowski C, Cooper B, Paul SM et al (2012) Identification of patient subgroups and risk factors for persistent breast pain following breast cancer surgery. J Pain 13:1172–1187CrossRefPubMedPubMedCentral
6.
go back to reference Karki A, Simonen R, Malkia E et al (2005) Impairments, activity limitations and participation restrictions 6 and 12 months after breast cancer operation. J Rehabil Med 37:180–188PubMed Karki A, Simonen R, Malkia E et al (2005) Impairments, activity limitations and participation restrictions 6 and 12 months after breast cancer operation. J Rehabil Med 37:180–188PubMed
7.
go back to reference Feiten S, Dunnebacke J, Heymanns J et al (2014) Breast cancer morbidity: questionnaire survey of patients on the long term effects of disease and adjuvant therapy. Dtsch Arztebl Int 111:537–544PubMedPubMedCentral Feiten S, Dunnebacke J, Heymanns J et al (2014) Breast cancer morbidity: questionnaire survey of patients on the long term effects of disease and adjuvant therapy. Dtsch Arztebl Int 111:537–544PubMedPubMedCentral
8.
go back to reference Norman SA, Localio AR, Kallan MJ et al (2010) Risk factors for lymphedema after breast cancer treatment. Cancer Epidemiol Biomark Prev 19:2734–2746CrossRef Norman SA, Localio AR, Kallan MJ et al (2010) Risk factors for lymphedema after breast cancer treatment. Cancer Epidemiol Biomark Prev 19:2734–2746CrossRef
9.
go back to reference Crew KD, Greenlee H, Capodice J et al (2007) Prevalence of joint symptoms in postmenopausal women taking aromatase inhibitors for early-stage breast cancer. J Clin Oncol 25:3877–3883CrossRefPubMed Crew KD, Greenlee H, Capodice J et al (2007) Prevalence of joint symptoms in postmenopausal women taking aromatase inhibitors for early-stage breast cancer. J Clin Oncol 25:3877–3883CrossRefPubMed
10.
go back to reference DiSipio T, Rye S, Newman B et al (2013) Incidence of unilateral arm lymphoedema after breast cancer: a systematic review and meta-analysis. Lancet Oncol 14:500–515CrossRefPubMed DiSipio T, Rye S, Newman B et al (2013) Incidence of unilateral arm lymphoedema after breast cancer: a systematic review and meta-analysis. Lancet Oncol 14:500–515CrossRefPubMed
11.
12.
go back to reference Kornblith AB, Lan L, Archer L et al (2011) Quality of life of older patients with early-stage breast cancer receiving adjuvant chemotherapy: a companion study to cancer and leukemia group B 49907. J Clin Oncol 29:1022–1028CrossRefPubMedPubMedCentral Kornblith AB, Lan L, Archer L et al (2011) Quality of life of older patients with early-stage breast cancer receiving adjuvant chemotherapy: a companion study to cancer and leukemia group B 49907. J Clin Oncol 29:1022–1028CrossRefPubMedPubMedCentral
13.
go back to reference Cancer Therapy Evaluation Program, Common Toxicity Criteria (CTC) Version 2.0, 1999 Cancer Therapy Evaluation Program, Common Toxicity Criteria (CTC) Version 2.0, 1999
14.
go back to reference Mantel N (1963) Chi Square tests with one degree of freedom; extensions of the Mantel-Haenszel procedure. J Am Stat Assoc 58:690–700 Mantel N (1963) Chi Square tests with one degree of freedom; extensions of the Mantel-Haenszel procedure. J Am Stat Assoc 58:690–700
15.
go back to reference Sakorafas GH, Peros G, Cataliotti L et al (2006) Lymphedema following axillary lymph node dissection for breast cancer. Surg Oncol 15:153–165CrossRefPubMed Sakorafas GH, Peros G, Cataliotti L et al (2006) Lymphedema following axillary lymph node dissection for breast cancer. Surg Oncol 15:153–165CrossRefPubMed
16.
go back to reference Kotronoulas G, Kearney N, Maguire R et al (2014) What is the value of the routine use of patient-reported outcome measures toward improvement of patient outcomes, processes of care, and health service outcomes in cancer care? A systematic review of controlled trials. J Clin Oncol 32:1480–1501CrossRefPubMed Kotronoulas G, Kearney N, Maguire R et al (2014) What is the value of the routine use of patient-reported outcome measures toward improvement of patient outcomes, processes of care, and health service outcomes in cancer care? A systematic review of controlled trials. J Clin Oncol 32:1480–1501CrossRefPubMed
17.
go back to reference Pedro-Guzman J (2016) Managing Upper Extremity Dysfunction in Breast Cancer Survivors Pedro-Guzman J (2016) Managing Upper Extremity Dysfunction in Breast Cancer Survivors
18.
go back to reference Smoot B, Wong J, Cooper B et al (2010) Upper extremity impairments in women with or without lymphedema following breast cancer treatment. J Cancer Surviv 4:167–178CrossRefPubMedPubMedCentral Smoot B, Wong J, Cooper B et al (2010) Upper extremity impairments in women with or without lymphedema following breast cancer treatment. J Cancer Surviv 4:167–178CrossRefPubMedPubMedCentral
19.
go back to reference Lucci A, McCall LM, Beitsch PD et al (2007) Surgical complications associated with sentinel lymph node dissection (SLND) plus axillary lymph node dissection compared with SLND alone in the American College of Surgeons Oncology Group Trial Z0011. J Clin Oncol 25:3657–3663CrossRefPubMed Lucci A, McCall LM, Beitsch PD et al (2007) Surgical complications associated with sentinel lymph node dissection (SLND) plus axillary lymph node dissection compared with SLND alone in the American College of Surgeons Oncology Group Trial Z0011. J Clin Oncol 25:3657–3663CrossRefPubMed
20.
go back to reference Ashikaga T, Krag DN, Land SR et al (2010) Morbidity results from the NSABP B-32 trial comparing sentinel lymph node dissection versus axillary dissection. J Surg Oncol 102:111–118CrossRefPubMedPubMedCentral Ashikaga T, Krag DN, Land SR et al (2010) Morbidity results from the NSABP B-32 trial comparing sentinel lymph node dissection versus axillary dissection. J Surg Oncol 102:111–118CrossRefPubMedPubMedCentral
21.
go back to reference Land SR, Kopec JA, Julian TB et al (2010) Patient-reported outcomes in sentinel node-negative adjuvant breast cancer patients receiving sentinel-node biopsy or axillary dissection: National Surgical Adjuvant Breast and Bowel Project phase III protocol B-32. J Clin Oncol 28:3929–3936CrossRefPubMedPubMedCentral Land SR, Kopec JA, Julian TB et al (2010) Patient-reported outcomes in sentinel node-negative adjuvant breast cancer patients receiving sentinel-node biopsy or axillary dissection: National Surgical Adjuvant Breast and Bowel Project phase III protocol B-32. J Clin Oncol 28:3929–3936CrossRefPubMedPubMedCentral
22.
go back to reference Gnant M, Thomssen C, Harbeck N (2015) St. Gallen/Vienna 2015: a brief summary of the consensus discussion. Breast Care (Basel) 10:124–130CrossRef Gnant M, Thomssen C, Harbeck N (2015) St. Gallen/Vienna 2015: a brief summary of the consensus discussion. Breast Care (Basel) 10:124–130CrossRef
23.
go back to reference Meretoja TJ, Leidenius MH, Tasmuth T et al (2014) Pain at 12 months after surgery for breast cancer. JAMA 311:90–92CrossRefPubMed Meretoja TJ, Leidenius MH, Tasmuth T et al (2014) Pain at 12 months after surgery for breast cancer. JAMA 311:90–92CrossRefPubMed
Metadata
Title
Lymphedema, musculoskeletal events and arm function in older patients receiving adjuvant chemotherapy for breast cancer (Alliance A171302)
Authors
Judith O. Hopkins
Jake Allred
Arti Hurria
Aminah Jatoi
Jacqueline M. Lafky
Harvey Cohen
Clifford Hudis
Eric Winer
Jeanne Mandelblatt
Ann Partridge
Lisa Carey
Hyman B. Muss
Publication date
01-12-2017
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 3/2017
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-017-4454-7

Other articles of this Issue 3/2017

Breast Cancer Research and Treatment 3/2017 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine