4.6 Article

Prediction of survival after eribulin chemotherapy for breast cancer by absolute lymphocyte counts and progression types

Journal

WORLD JOURNAL OF SURGICAL ONCOLOGY
Volume 19, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12957-021-02441-w

Keywords

Eribulin; Breast cancer; RECIST; Prognostic marker; Absolute lymphocyte counts

Funding

  1. Ministry of Education, Science, Sports, Culture and Technology of Japan [19K18067, 17K10559, 20K08938]
  2. Grants-in-Aid for Scientific Research [17K10559, 19K18067, 20K08938] Funding Source: KAKEN

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The study found that patients with progression by preexisting disease (PPL) had better survival rates than those with progression by new metastases (PNM) in patients treated with eribulin. Additionally, breast cancer patients with ALC >= 1500/mu l were associated with less progression, particularly metastasis, and better prognosis. In addition, the biomarker high-ALC (ALC >= 1500/mu l) and PPL were particularly useful as prognostic markers following eribulin chemotherapy.
Background In the Response Evaluation Criteria for Solid Tumors (RECIST) diagnostic criteria, the concepts of progression by preexisting disease (PPL) and progression by new metastases (PNM) have been proposed to distinguish between the progression types of cancer refractory to treatment. According to the tumor biology of cancer progression forms, the PPL form indicates invasion, and the PNM form indicates metastasis. On the other hand, recent studies have focused on the clinical importance of inflammatory markers as indicators of the systemic tumor immune response. In particular, absolute lymphocyte count (ALC) is an indicator of the host's immune response. Thus, we developed a new measure that combined progression form with ALC. In this study, we clinically validated the combined assessment of progression form and ALC in eribulin chemotherapy. Methods From August 2011 to April 2019, a total of 486 patients with locally advanced or metastatic breast cancer (MBC) underwent treatment. In this study, only 88 patients who underwent chemotherapy using eribulin were included. The antitumor effect was evaluated based on the RECIST criteria, version 1.1. To measure ALC, peripheral blood samples collected before eribulin treatment were used. The cut-off value for ALC in this study was 1500/mu l, based on previous studies. Results The PPL group (71 patients, 80.7%) had significantly longer progression-free survival (PFS) (p = 0.022, log-rank) and overall survival (OS) (p < 0.001, log-rank) than the PNM group (17 patients, 19.3%). In the 51 patients with ALC < 1500/mu l, the PPL group had a significantly better prognosis than the PNM group (PFS: p = 0.035, OS: p < 0.001, log-rank, respectively). On the other hand, in the 37 patients with ALC >= 1500/mu l, the PPL group had a better OS compared with the PNM group (p = 0.055, log-rank), but there was no significant difference in PFS between the two groups (p = 0.541, log-rank). Furthermore, multivariate analysis that validated the effect of OS showed that high ORR and high-ALC and PPL were factors for a good prognosis (p < 0.001, HR = 0.321; p = 0.036, HR = 0.290). Conclusions The progression form of PNM had a worse prognosis than PPL in patients treated with eribulin. In breast cancer patients with eribulin chemotherapy, good systemic immune status, such as ALC >= 1500/mu l, was associated with less progression, particularly metastasis, and better prognosis. Furthermore, the biomarker high-ALC (ALC >= 1500/mu l) and PPL was particularly useful as a prognostic marker following eribulin chemotherapy.

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