TY - JOUR
T1 - Immune checkpoint inhibitors for patients with metastatic triple-negative inflammatory breast cancer (INCORPORATE)
T2 - An international cohort study
AU - Valenza, Carmine
AU - Trapani, Dario
AU - Zagami, Paola
AU - Antonarelli, Gabriele
AU - Boscolo Bielo, Luca
AU - Nicolò, Eleonora
AU - Ribeiro, Joana Mourato
AU - Guidi, Lorenzo
AU - Reduzzi, Carolina
AU - Spotti, Martina
AU - Adamoli, Laura
AU - Cortès, Javier
AU - Pistilli, Barbara
AU - Tolaney, Sara M.
AU - Ueno, Naoto
AU - Layman, Rachel M.
AU - Cristofanilli, Massimo
AU - Carey, Lisa A.
AU - Munzone, Elisabetta
AU - Criscitiello, Carmen
AU - Lynce, Filipa
AU - Woodward, Wendy A.
AU - Curigliano, Giuseppe
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/12/1
Y1 - 2024/12/1
N2 - Background: Inflammatory breast cancer (IBC) is the most aggressive clinical presentation of breast cancer, recapitulating a specific biology with more immune-vulnerability than non-IBC. Patients with metastatic, triple-negative IBC (mTN-IBC) receive immune checkpoint inhibitors (ICIs) and chemotherapy, similarly to patients with triple-negative non-IBC. However, the benefit derived from ICI incorporation in this rare type of breast cancer is unknown. Methods: We conducted a multicenter, international, retrospective, cohort study to evaluate the activity of ICIs in patients with metastatic, triple-negative, primary IBC, who received ICIs plus first line chemotherapy from January 2015 to April 2023. A sample size of 42 patients allowed to detect an increase in 6-months real-world progression-free survival (rwPFS) rate from 40 % with only chemotherapy to 60 % with ICI and chemotherapy. Results: 41 patients from eight international IBC referral centers were included (61 % with primary, de novo mTN-IBC, 61 % with visceral disease). All received ICIs plus first line chemotherapy and 24 % underwent breast surgery and/or locoregional radiotherapy. After a median follow-up of 19.3 months, the 6-months rwPFS rate was 30 % (95 % Confidence Interval [CI], 17–45 %), the median rwPFS was 3.3 months (95 % CI: 2.2–5.4), the median overall survival was 15.7 months (95 % CI: 6.8–16.3). Conclusions: This one-sample analysis showed a poor outcome of patients with mTN-IBC, despite the treatment with ICI, in contrast with the expected benefit based on preclinical evidence of immune-vulnerability of IBC. These results suggest the need to further investigate the role of immunotherapy in this aggressive and rare type of breast cancer presentation.
AB - Background: Inflammatory breast cancer (IBC) is the most aggressive clinical presentation of breast cancer, recapitulating a specific biology with more immune-vulnerability than non-IBC. Patients with metastatic, triple-negative IBC (mTN-IBC) receive immune checkpoint inhibitors (ICIs) and chemotherapy, similarly to patients with triple-negative non-IBC. However, the benefit derived from ICI incorporation in this rare type of breast cancer is unknown. Methods: We conducted a multicenter, international, retrospective, cohort study to evaluate the activity of ICIs in patients with metastatic, triple-negative, primary IBC, who received ICIs plus first line chemotherapy from January 2015 to April 2023. A sample size of 42 patients allowed to detect an increase in 6-months real-world progression-free survival (rwPFS) rate from 40 % with only chemotherapy to 60 % with ICI and chemotherapy. Results: 41 patients from eight international IBC referral centers were included (61 % with primary, de novo mTN-IBC, 61 % with visceral disease). All received ICIs plus first line chemotherapy and 24 % underwent breast surgery and/or locoregional radiotherapy. After a median follow-up of 19.3 months, the 6-months rwPFS rate was 30 % (95 % Confidence Interval [CI], 17–45 %), the median rwPFS was 3.3 months (95 % CI: 2.2–5.4), the median overall survival was 15.7 months (95 % CI: 6.8–16.3). Conclusions: This one-sample analysis showed a poor outcome of patients with mTN-IBC, despite the treatment with ICI, in contrast with the expected benefit based on preclinical evidence of immune-vulnerability of IBC. These results suggest the need to further investigate the role of immunotherapy in this aggressive and rare type of breast cancer presentation.
KW - Immune checkpoint inhibitors
KW - Immunotherapy
KW - Inflammatory breast cancer
KW - Triple-negative breast cancer
UR - http://www.scopus.com/inward/record.url?scp=85207775032&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2024.115097
DO - 10.1016/j.ejca.2024.115097
M3 - Article
AN - SCOPUS:85207775032
SN - 0959-8049
VL - 213
JO - European Journal of Cancer
JF - European Journal of Cancer
M1 - 115097
ER -