Tailored Axillary Surgery With or Without Axillary Lymph Node Dissection Followed by Radiotherapy in Patients With Clinically Node-positive Breast Cancer (TAXIS)
1500 patients around the world
Available in Argentina
The removal of all lymph nodes in the armpit through conventional axillary dissection has
been standard care for all patients with breast cancer for almost a century. In the nineties,
the sentinel lymph node procedure, which involves the selective removal of the first few
affected lymph nodes, was introduced in clinical practice. Today, conventional axillary
dissection is still performed on many women with breast cancer that has spread to the nodes.
It is the cause for relevant morbidity in the form of lymphedema, impairment of shoulder
mobility, sensation disorders and chronic pain in as much as one third of all women
undergoing the procedure.
The TAXIS trial will evaluate the optimal treatment for breast cancer patients in terms of
surgery and radiotherapy. In particular, it will investigate the value of tailored axillary
surgery (TAS), a new technique that aims at selectively removing the positive lymph nodes.
TAS combines the removal of palpably suspicious nodes with the sentinel procedure. TAS is a
promising procedure that may significantly decrease morbidity in breast cancer patients by
avoiding surgical overtreatment.
This trial has the potential to establish a new worldwide treatment standard with hopefully
less side effects and a better quality of life, while keeping the same efficacy as provided
by radical surgery.
The main objective of the trial is to show that TAS and axillary radiotherapy (RT) is
non-inferior to ALND in terms of disease-free survival of node positive breast cancer
patients at high risk of recurrence in the era of effective systemic therapy and extended
regional nodal irradiation.
University Hospital, Basel, Switzerland
1Research sites
1500Patients around the world
This study is for people with
Breast Cancer
Requirements for the patient
From 18 Years
All Gender
Medical requirements
Inclusion criteria at pre-registration: written informed consent according to ICH/GCP regulations prior to any trial specific procedures.
Inclusion criteria at pre-registration: breast cancer, node positive detected by palpation or imaging (with or without planned neoadjuvant treatment).
Inclusion criteria at pre-registration: female or male aged ≥ 18 years.
Inclusion criteria at pre-registration: ability to complete the Quality of Life questionnaires.
Inclusion criteria at registration: node-positive breast cancer (histologically or cytologically proven both in primary tumor and in lymph node) AJCC/UICC [42] stage II-III (all molecular subtypes allowed).
Inclusion criteria at registration: node-positivity detected by imaging (iN+) and confirmed by pathology.
Inclusion criteria at registration: node-positivity detected by palpation (cN1-3) and confirmed by pathology.
Inclusion criteria at registration: occult breast cancer is allowed, if biopsy-proven axillary lymphatic metastasis is present.
Inclusion criteria at registration: eligible for primary ALND or sentinel lymph node (SLN) procedure with frozen section and either:
newly diagnosed,
isolated in-breast recurrence or second ipsilateral breast cancer after previous breast conserving surgery and sentinel procedure and at least 3 years disease free and no prior axillary dissection or axillary RT.
Inclusion criteria at registration: most suspicious axillary lymph node clipped.
Inclusion criteria at registration: baseline Quality of Life questionnaire has been completed.
Inclusion criteria at registration: WHO performance status 0-2.
Inclusion criteria at registration: adequate condition for general anesthesia and breast cancer surgery.
Inclusion criteria at registration: women with child-bearing potential are using effective contraception, are not pregnant or lactating and agree not to become pregnant during trial treatment and thereafter during the time recommended by the guidelines for adjuvant systemic therapies. A negative pregnancy test before inclusion into the trial is required for all women with child-bearing potential.
Inclusion criteria at registration: men agree not to father a child during trial treatment and thereafter during 6 months.
Inclusion criteria at randomization (intraoperatively): node-positive breast cancer (histologically or cytologically proven both in primary tumor and in lymph node) AJCC/UICC stage II-III (all molecular subtypes allowed).
Inclusion criteria at randomization (intraoperatively): Node-positive breast cancer (histologically or cytologically proven both in primary tumor and in lymph node) AJCC/UICC stage II-III (all molecular subtypes allowed):
node-positivity initially detected by imaging and non-palpable and residual disease confirmed by pathology** (including residual ITCs) in SLN or non SLN in case of prior neoadjuvant treatment.
node-positivity initially palpable and residual disease confirmed by pathology** (including residual ITCs) in case of prior neoadjuvant treatment.
*Note: patients with ypN0(i+) can be included (the AJCC stage II-III refers to the stage before neoadjuvant treatment) **note: if the fine needle aspiration or core biopsy of the clipped node after neoadjuvant treatment unequivocally shows cancer, repeated confirmation of residual disease by intraoperative frozen section is not mandatory.
Exclusion criteria at pre-registration: stage IV breast cancer.
Exclusion criteria at pre-registration: clinical N3c breast cancer (clinical N3a and clinical N3b are allowed).
Exclusion criteria at pre-registration: clinical N2b breast cancer (clinical N2a is allowed).
Exclusion criteria at pre-registration: contralateral breast cancer within 3 years note: contralateral ductal carcinoma in situ (DCIS) is allowed if prior treatment does not interfere with or compromise the trial treatment.
Exclusion criteria at pre-registration: prior axillary surgery (except prior sentinel node procedure in case of in- breast recurrence).
Exclusion criteria at pre-registration: prior regional radiotherapy.
Exclusion criteria at pre-registration: history of hematologic or primary solid tumor malignancy, unless in remission for at least 3 years from pre-registration with the exception of adequately treated cervical carcinoma in situ or localized non-melanoma skin cancer.
Exclusion criteria at pre-registration: treatment with any experimental drug within 30 days of pre-registration.
Exclusion criteria at pre-registration: any other serious underlying medical, psychiatric, psychological, familial or geographical condition, which in the judgment of the investigator may interfere with the planned staging, treatment and follow-up, affect patient compliance or place the patient at high risk from treatment-related complications.
Exclusion criteria at randomization (intraoperatively): absence of clip in the specimen radiography.
Exclusion criteria at randomization (intraoperatively): palpable disease left behind in the axilla after Tailored Axillary Surgery (TAS).
Exclusion criteria at randomization (intraoperatively): no SLN identified in the axilla.
Sites
Instituto de Oncología Ángel H. Roffo - CABA, Buenos Aires