Evidence map›Paper›PMID 39019875›Full record

ArticleNPJ breast cancer2024

Differential effects of desvenlafaxine on hot flashes in women with breast cancer taking tamoxifen: a randomized controlled trial.

Yongjoo Kim, Chan-Woo Yeom, Hyun Jeong Lee, Jeong-Hyun Kim, Kwang-Min Lee, Tae-Yong Kim, Han-Byoel Lee, Hoon Kim, Seock-Ah Im, Kyung-Hun Lee and 6 more

Registry-linked trialAbstract read
In one paragraph

Article in NPJ breast cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02819921 (Desvenlafaxine for the Treatment of Hot Flashes in Women With Breast Cancer Taking Tamoxifen), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT02819921 phase4terminatednot on this map

Desvenlafaxine for the Treatment of Hot Flashes in Women With Breast Cancer Taking Tamoxifen: a Randomized, Double-blind, Placebo-controlled Study

TypeinterventionalSponsorSeoul National University HospitalRan2017 to 2019Enrolled59ConditionsHot Flashes, Breast NeoplasmsArmsDesvenlafaxine succinate 100mg, Desvenlafaxine succinate 50mg, Placebo
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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

16 authors.

Yongjoo Kim *College of Korean Medicine, Sangji University, Wonju, Republic of Korea.ORCID http://orcid.org/0000-0002-0768-9256
Chan-Woo Yeom *Department of Psychiatry, Uijeongbu Eulji Medical Center, Uijeongbu, Republic of Korea.
Hyun Jeong LeeMental Health Clinic, National Cancer Center, Goyang, Republic of Korea.
Jeong-Hyun KimDepartment of Psychiatry, Seoul National University Bundang Hospital, Seongnam, Republic of Korea.
Kwang-Min LeeMind Lab Place Psychiatry Clinic, Seoul, Republic of Korea.
Tae-Yong KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Han-Byoel LeeDepartment of Surgery, Seoul National University Hospital, Seoul, Republic of Korea.
Hoon KimDepartment of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Seock-Ah ImDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Kyung-Hun LeeDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Miso KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Wonsik HanDepartment of Surgery, Seoul National University Hospital, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0001-7310-0764
Hyeong-Gon MoonDepartment of Surgery, Seoul National University Hospital, Seoul, Republic of Korea.
David SpiegelDepartment of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA.
Bong-Jin HahmDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
Kyung-Lak SonDepartment of Psychiatry, Dongguk University Ilsan Hospital, Goyang, Republic of Korea. klson01@gmail.com.ORCID http://orcid.org/0000-0002-9332-8659

Funding

Pfizer (Pfizer Inc.) 53232755
6 · The paper itself

Abstract

Hot flashes (HF) are a common adverse event of prolonged tamoxifen use in women with estrogen receptor-positive breast cancer, impacting psychiatric health and quality of life. While desvenlafaxine does not interact with tamoxifen, its efficacy and safety in breast cancer patients remain unstudied. This phase 3, four-week, multi-center, three-arm, parallel-group, randomized, double-blind, placebo-controlled trial investigated the efficacy and safety of desvenlafaxine for treating HF in women with breast cancer taking tamoxifen, assessing potential differential effects in patients with psychiatric and inflammatory conditions. Between December 2017 and February 2019, 57 women aged 19 or older, regularly taking tamoxifen as adjuvant therapy, experiencing moderate-to-severe HFs for more than a month, were randomized to receive desvenlafaxine 50 mg/day (D-50), desvenlafaxine 100 mg/day (D-100), or placebo for four weeks. The primary endpoint was the change rate in HF scores over four weeks, with adverse events as a secondary endpoint. Both desvenlafaxine arms demonstrated greater HF score reductions compared to placebo: D-50 (2.20 points/week, 95% CI: 0.71, 3.68) and D-100 (2.34 points/week, 95% CI: 0.92, 3.76). Notably, D-50 arm showed significantly greater efficacy in patients with depression or elevated inflammation. Desvenlafaxine offers an effective and safe treatment regimen for HF in women with breast cancer taking tamoxifen. The presence of depression and inflammation may guide optimal desvenlafaxine dosing. (Trial Registration: ClinicalTrials.gov Identifier: NCT02819921).

Identifiers

PMID39019875
PMCPMC11255222

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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.