Evidence map›Paper›PMID 32495001›Full record

ArticleBreast cancer research and treatment2020

Low-dose metronomic chemotherapy as an efficient treatment option in metastatic breast cancer-results of an exploratory case-control study.

S Krajnak, C Schnatz, K Almstedt, W Brenner, F Haertner, A-S Heimes, A Lebrecht, G-M Makris, R Schwab, A Hasenburg and 2 more

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Breast cancer research and treatment, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 27% of its field
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

13 citing papers in PubMed, 22 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

S KrajnakDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany. slavomir.krajnak@unimedizin-mainz.de.ORCID http://orcid.org/0000-0002-8012-5772
C SchnatzDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany.
K AlmstedtDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany.
W BrennerDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany.
F HaertnerInstitute of Medical Biometry, Epidemiology and Informatics (IMBEI), University Medical Center Mainz, Mainz, Germany.
A-S HeimesDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany.
A LebrechtDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany.
G-M MakrisDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany.
R SchwabDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany.
A HasenburgDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany.
M SchmidtDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany.
M J BattistaDepartment of Gynecology and Obstetrics, University Medical Center Mainz, Langenbeckstrasse 1, 55131, Mainz, Germany.
Johannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThere is growing interest in low-dose metronomic chemotherapy (LDMC) in metastatic breast cancer (MBC). In this retrospective case-control analysis, we compared the efficacy of LDMC and conventional chemotherapy (CCT) in MBC.

methodsEach LDMC patient receiving oral cyclophosphamide (CTX) (50 mg daily) and methotrexate (MTX) (2.5 mg every other day) was matched with two controls who received CCT. Age, number of chemotherapy lines and metastatic sites as well as hormone receptor (HR) status were considered as matching criteria. Primary endpoint was disease control rate longer than 24 weeks (DCR). Secondary endpoints were progression-free survival (PFS), duration of response (DoR) and subgroup analyses using the matching criteria.

results40 cases and 80 controls entered the study. 30.0% patients with LDMC and 22.5% patients with CCT showed DCR (p = 0.380). The median PFS was 12.0 weeks in both groups (p = 0.218) and the median DoR was 31.0 vs. 20.5 weeks (p = 0.383), respectively. Among younger patients, DCR was 40.0% in LDMC vs. 25.0% in the CCT group (p = 0.249). DCR was achieved in 33.3% vs. 26.2% non-heavily pretreated patients (p = 0.568) and in 36.0% vs. 18.0% patients without multiple metastases (p = 0.096), respectively. In the HR-positive group, 30.0% LDMC vs. 28.3% CCT patients showed DCR (p = 1.000). Among triple-negative patients, DCR was achieved in 30.0% LDMC and 5.0% CCT patients (p = 0.095).

conclusionsWe demonstrated a similar efficacy of LDMC compared to CCT in the treatment of MBC. Thus, LDMC may be a valuable treatment option in selected MBC patients.

Indexed as

Administration, MetronomicAdministration, OralAdultAgedAged, 80 and overAntineoplastic AgentsBreast NeoplasmsCase-Control StudiesChemotherapy, AdjuvantCyclophosphamideDose-Response Relationship, DrugErb-b2 Receptor Tyrosine KinasesFemaleHumansKaplan-Meier EstimateMastectomyAntineoplastic AgentsCyclophosphamideERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMethotrexateReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID32495001
PMCPMC7297707
OpenAlexW3031922078

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.