Evidence map›Paper›PMID 42032324›Full record

ReviewAnnals of hematology2026

Teclistamab for multiple pulmonary lesions in extramedullary myeloma: first successful case and review of the literature.

Teruhito Takakuwa, Kensuke Ohta, Yusuke Tanada, Yusuke Okayama, Masayuki Hino

Abstract readCase ReportsReview
In one paragraph

Review in Annals of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Teruhito TakakuwaDepartment of Hematology, Wakakusa-Daiichi Hospital, 1-6, wakakusa-cho, Higashi-osaka, Osaka, 579-8056, Japan. t_takakuwa@omu.ac.jp.
Kensuke OhtaHematology Ohta Clinic, Shinsaibashi, Osaka, Japan.
Yusuke TanadaDepartment of Hematology, Wakakusa-Daiichi Hospital, 1-6, wakakusa-cho, Higashi-osaka, Osaka, 579-8056, Japan.
Yusuke OkayamaDepartment of Hematology, Wakakusa-Daiichi Hospital, 1-6, wakakusa-cho, Higashi-osaka, Osaka, 579-8056, Japan.
Masayuki HinoDepartment of Hematology, Wakakusa-Daiichi Hospital, 1-6, wakakusa-cho, Higashi-osaka, Osaka, 579-8056, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extramedullary disease (EMD) in multiple myeloma (MM) is associated with aggressive clinical behavior and poor prognosis, particularly when involving the lung parenchyma, which is an extremely rare manifestation. Bispecific antibodies targeting B-cell maturation antigen (BCMA), such as teclistamab, have recently demonstrated promising efficacy in heavily pretreated relapsed/refractory multiple myeloma (RRMM). However, evidence regarding their activity in patients with pulmonary extramedullary involvement remains limited. We report the case of a 76-year-old man with IgA-κ RRMM who developed multiple extramedullary lesions, including pulmonary nodules, after progression on several lines of therapy. Following initiation of teclistamab, the patient experienced grade 1 cytokine release syndrome that resolved rapidly after tocilizumab administration. An abdominal wall mass transiently enlarged early after treatment initiation, raising suspicion of pseudoprogression. Subsequently, all extramedullary lesions, including the pulmonary nodules, showed marked regression, with complete radiologic resolution observed by day 80. At 4.5 months after treatment initiation, both positron emission tomography–computed tomography and bone marrow multiparameter flow cytometry demonstrated minimal residual disease negativity. The patient has continued teclistamab therapy with sustained disease control. This case illustrates that teclistamab may provide meaningful clinical benefit even in RRMM with pulmonary extramedullary involvement, a condition typically associated with extremely poor outcomes. Our findings also suggest that transient lesion enlargement early after therapy may represent pseudoprogression and should be interpreted cautiously in patients receiving bispecific antibody therapy.

Indexed as

Antibodies, BispecificLung NeoplasmsMultiple MyelomaAgedHumansMaleAntibodies, BispecificBispecific antibodyExtramedullary diseasePulmonary involvementRelapsed/refractory multiple myelomaTeclistamab

Identifiers

PMID42032324
PMCPMC13109173

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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.