Content - SAKK 23/16 TAXIS

SAKK 23/16 TAXIS – Surgical lymph node removal with the option of “extensive operation” or “radiotherapy” in breast cancer patients with existing axillary lymph node involvement

In this study, we are investigating the efficacy of radiotherapy compared to surgery in the treatment of breast cancer with axillary lymph node involvement.  We are conducting this study to discover the most effective treatment with the fewest side effects.

The study schedule is as follows: A limited number of affected lymph nodes and the sentinel nodes will be surgically removed from all patients. The patients will then be assigned to one of two groups on a random basis (randomized study).

In one group, the remaining lymph nodes in the axilla will be removed. This corresponds to the standard treatment for effectively preventing recurrences in the axilla. However, side effects – permanent in some cases – persist in about one quarter of patients. Such effects include impaired sensation, chronic pain, restricted movement in the shoulder and swelling of the arm, known as lymphoedema.

In the other group, the axilla will be irradiated. This treatment can sometimes be just as effective as the treatment for the first group and cause fewer side effects. If the benefit of the radiotherapy is confirmed in this study, this may become the new standard treatment for patients with this disease.

This study will be conducted at numerous centres in Switzerland and other countries. In total, we plan to recruit 1,500 patients (women and men with breast cancer) over a period of just over 5 years. The whole study will last for about 25 years, including the follow-up period. Medical visits will take place at frequent intervals at the start of the study and then annually from the third year of participation.

This important phase III trial will be conducted with generous support from Fond’Action, Krebsliga beider Basel, Stiftung Krebsforschung Schweiz, and The Rising Tide Foundation.

Study Chair:

Prof. Dr. med. Walter Weber, Basel University Hospital, +41 61 328 61 49

Locations for this trial:

Universitätsspital Basel
Petersgraben 4
0 4031 Basel