Evidence map›Paper›PMID 39526614›Full record

ArticleThe Journal of dermatology2025

Delayed and immediate cutaneous adverse events during pembrolizumab combination chemotherapy against cervical cancer: Case series.

Takeya Adachi, Tomoya Matsui, Utako Okata-Karigane, Chiaki Takahashi, Umi Tahara, Mari Hyodo, Akihiro Miyagawa, Kenta Kobayashi, Yoshio Nakamura, Takeru Funakoshi and 3 more

Abstract readCase Reports
In one paragraph

Article in The Journal of dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

13 authors.

Takeya AdachiDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0002-5289-5980
Tomoya MatsuiDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.
Utako Okata-KariganeDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Chiaki TakahashiDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Umi TaharaDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Mari HyodoDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Akihiro MiyagawaDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Kenta KobayashiDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0003-2615-1010
Yoshio NakamuraDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Takeru FunakoshiDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Hiroshi NishioDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4938-416X
Wataru YamagamiDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.
Hayato TakahashiDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.

Funding

Japan Agency for Medical Research and Development 23ek0410090Japan Agency for Medical Research and Development 23ek0410106Japan Society for the Promotion of Science JSPS KAKENHI 22K16268Scientific Research Fund of the Ministry of Health, Labour and Welfare, Japan 21FE2001
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs), such as pembrolizumab (PEM), are widely recognized for their antitumor efficacy, but they can also lead to various cutaneous adverse events (CAEs). While most CAEs can be managed with topical corticosteroids, severe cases may necessitate halting immunotherapy. The incidence of severe CAEs is notably higher in combination therapies involving ICIs than in monotherapies, emphasizing the need for stringent, long-term management strategies. This includes potential modifications or discontinuations of the combination therapy. PEM, when added to the conventional paclitaxel + cisplatin (or carboplatin) ± bevacizumab regimen, has shown significant improvements in overall and progression-free survival for patients with Stage IVB metastatic or locally uncontrolled recurrent cervical cancer. This case series retrospectively examined the incidence and management of CAEs in 19 female patients treated with this combination therapy between October 2022 and May 2023. Four patients exhibiting CTCAE grade 3 were identified. The four cases of severe CAEs involved erythema multiforme after the initial course of PEM combination chemotherapy. Notably, three patients experienced immediate hypersensitivity reactions, including anaphylaxis, during subsequent treatments. This observation underscores the necessity for rigorous dermatological monitoring of patients undergoing PEM combination chemotherapy. Such vigilance is crucial for early detection of adverse reactions and timely adjustment of treatment regimens, thereby enhancing patient safety.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsUterine Cervical NeoplasmsAdultAgedCarboplatinCisplatinDrug EruptionsFemaleHumansImmune Checkpoint InhibitorsIncidenceMiddle AgedPaclitaxelRetrospective StudiesAntibodies, Monoclonal, HumanizedCarboplatinCisplatinImmune Checkpoint InhibitorsPaclitaxelpembrolizumabanaphylaxiscervical cancererythema multiformeimmune checkpoint inhibitorpembrolizumab

Identifiers

PMID39526614
PMCPMC11700920

What OpenQuestion holds

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Registered trials

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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.