Evidence map›Paper›PMID 42033778›Full record

ArticleThe oncologist2026

Efficacy of perioperative pembrolizumab for triple-negative breast cancer with apocrine feature or metaplastic carcinoma.

Nobuyuki Takahashi, Chikako Funasaka, Mai Shimura, Akira Hirota, Mao Uematsu, Misao Fukuda, Kaede Baba, Kanako Mamishin, Hiromichi Nakajima, Chihiro Kondoh and 7 more

Abstract read
In one paragraph

Article in The oncologist, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Nobuyuki TakahashiDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.ORCID 0000-0002-8592-6528
Chikako FunasakaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.ORCID 0000-0003-0585-4884
Mai ShimuraDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Akira HirotaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Mao UematsuDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Misao FukudaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Kaede BabaDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Chiba, 277-8577, Japan.
Kanako MamishinDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Chiba, 277-8577, Japan.
Hiromichi NakajimaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Chihiro KondohDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Kenichi HaranoDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Nobuaki MatsubaraDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.ORCID 0000-0002-9203-4245
Ako HosonoDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Toshikatsu KawasakiDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Chiba, 277-8577, Japan.
Tatsuya OnishiDepartment of Breast Surgery, National Cancer Center Hospital East, Kashiwa, Chiba, 277-8577, Japan.
Yoichi NaitoDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.ORCID 0000-0002-8490-9064
Toru MukoharaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.ORCID 0000-0002-8573-418X

Funding

Young Investigator Funding of the Japan Health Research Promotion Bureau # 2022-wakate-08
6 · The paper itself

Abstract

backgroundThe KEYNOTE-522 (KN522) trial demonstrated significantly improved outcomes with neoadjuvant chemotherapy (NAC) combined with pembrolizumab in high-risk triple-negative breast cancer (TNBC). However, the efficacy of this chemoimmunotherapy for histologically uncommon TNBC subtypes, such as invasive ductal carcinoma (IDC) with apocrine feature (IDCapo) or metaplastic carcinoma, remains unclear. PATIENTS AND

methodsThis retrospective study examined clinicopathological characteristics and outcomes of patients with clinical stage II or III TNBC treated with either the KN522 regimen or conventional NAC without immunotherapy at the National Cancer Center Hospital East between August 2014 and December 2024. Patients pathologically diagnosed with IDC, IDCapo, or metaplastic carcinoma were included. We compared outcomes of the KN522 regimen among histologic subtypes and evaluated its efficacy versus conventional NAC in patients with IDCapo or metaplastic carcinoma.

resultsSeventy-two patients with TNBC received the KN522 regimen: 58 IDC, 10 IDCapo, and 4 metaplastic carcinoma. The pathological complete response (pCR) rate was significantly lower in IDCapo than in IDC (3/10 [30.0%] vs. 41/58 [70.7%], P = 0.027), and this difference remained after adjustment for clinical factors. There were no metaplastic carcinoma patients with pCR (0/4, 0%). Compared with conventional NAC, the KN522 regimen yielded a higher pCR rate in IDCapo (3/10 [30.0%] vs. 0/19 [0%], P = 0.033), but not in metaplastic carcinoma (0/4 [0%] vs. 1/10 [10.0%], P = 1.00).

conclusionThe pCR rate of NAC with pembrolizumab was significantly lower in IDCapo than in IDC but was improved compared with conventional NAC. No meaningful benefit was observed in metaplastic carcinoma. IMPLICATIONS FOR PRACTICE: This study suggests that neoadjuvant chemoimmunotherapy can improve pathological complete response rate in invasive ductal carcinoma with apocrine feature, known as therapeutically resistant uncommon histology of the breast cancer. Pathological complete response rates of the neoadjuvant chemoimmunotherapy is dismal in metaplastic breast carcinoma, which sheds light to highly unmet need of novel therapeutic strategies for such aggressive breast cancer.

Indexed as

Antibodies, Monoclonal, HumanizedCarcinoma, Ductal, BreastTriple Negative Breast NeoplasmsAdultAgedFemaleHumansMiddle AgedNeoadjuvant TherapyPathologic Complete ResponseRetrospective StudiesAntibodies, Monoclonal, HumanizedpembrolizumabBreast cancerimmunotherapyinvasive ductal carcinoma with apocrine featuremetaplastic carcinoma

Identifiers

PMID42033778
PMCPMC13166872

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.