Evidence map›Paper›PMID 30680210›Full record

ArticleMolecular and clinical oncology2019

Tolerability and safety of real-world use of pomalidomide in patients with relapsed/refractory multiple myeloma.

Eiseki Usami, Michio Kimura, Shoya Takenaka, Mina Iwai, Hitomi Teramachi, Tomoaki Yoshimura

Abstract read
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Article in Molecular and clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Eiseki UsamiDepartment of Pharmacy, Ogaki Municipal Hospital, Ogaki, Gifu 503-8502, Japan.
Michio KimuraDepartment of Pharmacy, Ogaki Municipal Hospital, Ogaki, Gifu 503-8502, Japan.
Shoya TakenakaDepartment of Pharmacy, Ogaki Municipal Hospital, Ogaki, Gifu 503-8502, Japan.
Mina IwaiDepartment of Pharmacy, Ogaki Municipal Hospital, Ogaki, Gifu 503-8502, Japan.
Hitomi TeramachiDepartment of Clinical Pharmacy, Gifu Pharmaceutical University, Gifu, Gifu 501-1196, Japan.
Tomoaki YoshimuraDepartment of Pharmacy, Ogaki Municipal Hospital, Ogaki, Gifu 503-8502, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pomalidomide (POM) is a second-generation immunomodulatory agent with proven efficacy in patients with relapsed/refractory multiple myeloma (RRMM) proven to be refractory to previous treatment with lenalidomide (LEN) and bortezomib. We herein conducted a retrospective analysis of 14 RRMM patients receiving POM to determine its tolerability and safety in the clinical setting. The median age of the patients was 72 years (range, 58-84 years), and 85.7% of the patients were aged >70 years. The most frequent treatment dose was 3 mg/day. POM dose reductions were required in 54.5% (6/11) of the patients. The patient data were compared among three age groups (<70, 70-75 and >75 years) and there was only significant difference in daily POM treatment dose. The tolerability of POM must be confirmed, particularly in elderly patients. Dose reduction from 4 to 3 mg occurred during the second cycle in 83.3% (5/6) of the patients. It is important to determine the tolerability of POM in the early phases of treatment. The most frequently reported grade 3/4 hematological adverse events were neutropenia (64.3%), anemia (64.3%) and thrombocytopenia (57.1%). Although the median number of treatment cycles was 4 (range, 1-13), 21.4% (3/14) of the patients with a performance status (PS) of 3 were administered only 1 treatment cycle. The tolerability of POM was low among patients with poor PS and an aggressive treatment introduction should be avoided. However, 21.4% (3/14) of the patients were able to continue treatment for >1 year and some patients received long-term therapy. POM does not require dose modification for renal function, and multiple capsule doses are available, which is an advantage of POM compared with LEN. POM may be administered to late-stage RRMM patients in a real-world clinical setting, but elderly patients or those with poor PS must be treated with caution. In this manner, the treatment options for RRMM patients may be expanded by assessing the tolerability and safety of POM.

Indexed as

pomalidomidereal-world userelapsed/refractory multiple myelomatolerability

Identifiers

PMID30680210
PMCPMC6327207

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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.