Evidence map›Paper›PMID 39562006›Full record

ArticleJournal for immunotherapy of cancer2024

Successful treatment of in-transit metastatic melanoma with combination intralesional T-VEC and topical imiquimod immunotherapy.

Marisa Lenga, Esther Choi, Jeffrey Sosman, Sunandana Chandra, Danielle Lam, Kirsten Johnson, Lauren Schiemann, Jennifer Choi

Abstract readCase Reports
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. 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. Review
  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

8 authors.

Marisa Lenga *Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID 0009-0001-1089-6846
Esther Choi *Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Jeffrey SosmanDivision of Hematology Oncology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Sunandana ChandraDivision of Hematology Oncology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Danielle LamDivision of Hematology Oncology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Kirsten JohnsonDivision of Hematology Oncology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Lauren SchiemannDivision of Hematology Oncology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Jennifer ChoiDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA jennifer.choi@northwestern.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In-transit metastases of malignant melanoma pose a significant clinical challenge, particularly in patients with contraindications to systemic therapies. While surgical excision and systemic immunotherapies remain standard treatments, localized therapies such as intralesional talimogene laherparepvec (T-VEC) and topical imiquimod, which stimulate tumor-specific T-cell responses, have garnered increasing attention for their potential efficacy and tolerability. Although the individual efficacy of these therapies is well-documented, their combined use and their synergistic effects have not been well-documented. This case series reports on five patients with in-transit melanoma metastases treated with T-VEC and imiquimod at Northwestern Memorial Hospital from November 2018 to May 2023. Patients received a median of 13 (range 8-20) T-VEC injections over a median of 6 months (range 5-9), of which 4 of those months were with concurrent T-VEC and imiquimod cream. Four of the five patients achieved complete response (CR) by the end of the treatment course. One patient developed systemic progression during therapy, leading to early cessation of treatment. All patients with CR elected to continue topical imiquimod applications as maintenance following T-VEC for a median of 6 months (range 2-14 months). Only one of the four patients who achieved CR developed metastatic nodal disease 10 months after the last T-VEC injection. The three other patients are free of cutaneous and systemic disease 2-57 months after their last injection. All patients tolerated treatment well with zero patients discontinuing treatment due to side effects. These findings suggest that the combination of intralesional T-VEC and topical imiquimod can be an effective and safe treatment of in-transit metastases of malignant melanoma.

Indexed as

ImiquimodImmunotherapyMelanomaAdministration, TopicalAdultAgedAged, 80 and overBiological ProductsCombined Modality TherapyFemaleHerpesvirus 1, HumanHumansInjections, IntralesionalMaleMiddle AgedOncolytic VirotherapyBiological ProductsImiquimodtalimogene laherparepvecImmunotherapyIntralesionalMelanomaOncolytic virus

Identifiers

PMID39562006
PMCPMC11575392

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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.