NCT04889924
See how this trial matches your record
Connect MyChart to see which criteria your record clearly satisfies, which need a clinician’s review, and which appear to disqualify you. Your data is read in this browser tab and never sent to our servers.
This clinical trial is studying a new way to manage lymph nodes in patients with breast cancer who have completed treatment before surgery, such as chemotherapy or hormone therapy. Specifically, it looks at whether targeted radiation to the armpit can replace the surgical removal of several lymph nodes, known as axillary lymph node dissection. The goal is to see if radiation can effectively prevent the cancer from returning while lowering the risk of lymphedema, a painful swelling of the arm that often follows extensive surgery. If you participate, you will be assigned to receive either the traditional surgery to remove lymph nodes or axillary radiation therapy.
This study may be an option for you if you were diagnosed with stage T1 to T4 breast cancer that originally had little to no involvement in the lymph nodes. To qualify, you must have completed at least 70% of your planned chemotherapy or six months of hormone therapy, and your recent imaging should show that your cancer responded well to that treatment. If your surgeon finds cancer in one or two of your sentinel nodes after your initial treatment, you may be eligible. You should talk to your doctor about whether your specific type of cancer and your response to treatment make this study a safe choice for you, and discuss how the different approaches to treating the lymph nodes might impact your recovery and long-term quality of life.
Generated · Written by an AI model from the trial’s public ClinicalTrials.gov record. Not medical advice.
In the case of primary surgery, in patients with sentinel node involvement, it has already been shown that omitting axillary lymph node dissection (ALND), often combining axillary radiotherapy (RT), does not worsen the prognosis and does significantly reduce the appearance of lymphedema. However, patients who have received neoadjuvant systemic treatment cannot benefit from this option, even though in the majority of those who have responded well to treatment, a residual disease in the armpit is low, but there are no studies yet published that supports the possibility of not performing lymphadenectomy. The primary endpoint is to evaluate wether axillary radiotherapy (ART) presents a lower risk of lymphedema with respect to lymphadenectomy (ALND) in patients with breast cancer who, after neoadjuvant systemic treatment (NST), present the sentinel node affected. Likewise, we will evaluate recurrences and overall survival in both groups. Finally, we will analyze the quality of life of these patients.
Requires clinical discussion
Requires clinical discussion
Requires clinical discussion
Requires clinical discussion
Requires clinical discussion
Requires clinical discussion
GenesisCare Mater
Sydney, Australia
Gillian Lamoury · 02 + 9458 8050 · Gillian.Lamoury@health.nsw.gov.au
GenesisCare North Shore
Sydney, Australia
Gillian Lamoury · 02 + 8037 4100 · Gillian.Lamoury@health.nsw.gov.au
GenesisCare Frenchs Forest
Sydney, Australia
Gillian Lamoury · 02 + 9470 5300 · Gillian.Lamoury@health.nsw.gov.au
GenesisCare Norwest
Sydney, Australia
Tim Wang · 02 + 8811 8400 · tim.wang@genesiscare.com
GenesisCare Hurstville
Sydney, Australia
Gina Hesselberg · 02 + 8568 7600 · receptiononcologyhurstville@genesiscare.com