Evidence map›Paper›PMID 36100310›Full record

ArticleJournal for immunotherapy of cancer2022

Phase 1 study of C-CAR088, a novel humanized anti-BCMA CAR T-cell therapy in relapsed/refractory multiple myeloma.

Xiaoyan Qu, Gang An, Weiwei Sui, Tingyu Wang, Xian Zhang, Junfang Yang, Yan Zhang, Lu Zhang, Dan Zhu, Jiaqi Huang and 13 more

4 registry-linked trialsOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 23 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 4 pooled it
3.2field-weighted citation impact, top 6% of its field
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.

NCT03751293 phase1unknown statusnot on this map

A Phase Ⅰ Study Evaluating Safety and Efficacy of C-CAR088 Treatment in Subjects With Relapsed or Refractory Multiple Myeloma

TypeinterventionalSponsorHebei Yanda Ludaopei HospitalRan2019 to 2020Enrolled10ConditionsRelapsed or Refractory Multiple MyelomaArmsC-CAR088
NCT03815383 phase1unknown statusnot on this map

A Phase Ⅰ Study Evaluating Safety and Efficacy of C-CAR088 Treatment in Subjects With Relapsed or Refractory Multiple Myeloma

TypeinterventionalSponsorThe First Affiliated Hospital with Nanjing Medical UniversityRan2019 to 2021Enrolled12ConditionsRelapsed or Refractory Multiple MyelomaArmsC-CAR088
NCT04295018 phase1unknown statusnot on this map

A Phase # Study Evaluating Safety and Efficacy of C-CAR088 Treatment in Subjects With Relapsed or Refractory Multiple Myeloma

TypeinterventionalSponsorPeking Union Medical College HospitalRan2019 to 2021Enrolled10ConditionsMultiple MyelomaArmsC-CAR088
NCT04322292 phase1completednot on this map

A Phase Ⅰ Study Evaluating Safety and Efficacy of C-CAR088 Treatment in Subjects With Relapsed or Refractory Multiple Myeloma

TypeinterventionalSponsorInstitute of Hematology & Blood Diseases Hospital, ChinaRan2019 to 2022Enrolled9ConditionsMultiple MyelomaArmsC-CAR088
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 4 syntheses or guidelines pooled it, 31 citations in OpenAlex.

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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

23 authors at 5 institutions in 2 countries.

Xiaoyan Qu *Department of Hematology, First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Collaborative Innovation Center for Cancer Personalized Medicine, Nanjing, China.ORCID 0000-0003-0863-5417
Gang An *State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Weiwei SuiState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Tingyu WangState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Xian ZhangDepartment of hematology, Hebei Yanda Lu Daopei Hospital, Langfang, China.
Junfang YangDepartment of hematology, Hebei Yanda Lu Daopei Hospital, Langfang, China.
Yan ZhangDepartment of hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Lu ZhangDepartment of hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Dan ZhuCellular Biomedicine Group Inc, Shanghai, China.
Jiaqi HuangCellular Biomedicine Group Inc, Shanghai, China.
Shigui ZhuCellular Biomedicine Group Inc, Shanghai, China.
Xin YaoCellular Biomedicine Group Inc, Shanghai, China.
Jing LiCellular Biomedicine Group Inc, Shanghai, China.
Chengxiao ZhengCellular Biomedicine Group Inc, Shanghai, China.
Kevin ZhuUniversity of Maryland School of Medicine, Baltimore, Maryland, USA.
Yutian WeiCellular Biomedicine Group Inc, Shanghai, China.
Xiaoteng LvCellular Biomedicine Group Inc, Shanghai, China.
Liping LanCellular Biomedicine Group Inc, Shanghai, China.
Yihong YaoCellular Biomedicine Group Inc, Shanghai, China.
Daobin ZhouDepartment of hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Peihua LuDepartment of hematology, Hebei Yanda Lu Daopei Hospital, Langfang, China.
Lugui QiuState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Jianyong LiDepartment of Hematology, First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Collaborative Innovation Center for Cancer Personalized Medicine, Nanjing, China lijianyonglm@126.com.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNShanghai Cell Therapy Research Institute · CNJiangsu Province Hospital · CNLuye Pharma (China) · CNUniversity of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnti-B-cell maturation antigen (BCMA) chimeric antigen receptor T-cell (CAR T) therapy showed remarkable efficacy in patients with relapsed or refractory multiple myeloma (RRMM). This phase 1 dose-escalation and expansion study developed C-CAR088, a novel second-generation humanized anti-BCMA CAR T-cell therapy, and assessed the safety and efficacy of three dosages of C-CAR088 in patients with RRMM.

methodsPatients received lymphodepletion with three doses of cyclophosphamide (300 mg/m

resultsAs of July 2, 2021, 31 patients had been infused with C-CAR088. Any grade cytokine release syndrome (CRS) occurred in 29 patients (93.5%), and grade 3 CRS occurred in 3 patients (9.7%). One patient from the high-dose group (4.5-6.0×10

conclusionsThe present study demonstrated that C-CAR088 had a good safety profile and high antitumor activity in patients with RRMM, constituting a promising treatment option for RRMM. TRIAL REGISTRATION NUMBER: NCT03815383, NCT03751293, NCT04295018, and NCT04322292.

Indexed as

Multiple MyelomaReceptors, Chimeric AntigenCyclophosphamideHumansImmunotherapy, AdoptiveT-LymphocytesCyclophosphamideReceptors, Chimeric AntigenAntibodies, NeoplasmCostimulatory and Inhibitory T-Cell ReceptorsHematologic Neoplasms

Identifiers

PMID36100310
PMCPMC9472147
OpenAlexW4295754446

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.