Evidence map›Paper›PMID 29386072›Full record

ArticleJournal of hematology & oncology2018

Activity of pembrolizumab in relapsed/refractory NK/T-cell lymphoma.

Xin Li, Yasong Cheng, Mingzhi Zhang, Jiaqin Yan, Ling Li, Xiaorui Fu, Xudong Zhang, Yu Chang, Zhenchang Sun, Hui Yu and 8 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Journal of hematology & oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 127 papers.

0numbers the graph read from it
0cells of the map it votes in
127citing 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.

NCT04230330 phase1withdrawnnot on this mapstarted 2019, after this paper: background citation

A Pilot Study of Nivolumab in Combination With GDP (Gemcitabine, Dexamethasone, Cisplatin)/ L-asparaginase in Patients With Advanced Stage or Relapsed/ Refractory Natural-killer/ T-cell Lymphoma

TypeinterventionalSponsorNational Cancer Centre, SingaporeRan2019 to 2020Enrolled0ConditionsNK/T Cell LymphomaArmsIV Nivolumab, IV Gemcitabine, IV Cisplatin, IV/PO Dexamethasone, IV L-asparaginase
NCT05316246 phase2unknown statusnot on this mapstarted 2022, after this paper: background citation

Efficacy and Safety of Brentuximab Vedotin in Combination With Tislelizumab for the Treatment of CD30-positive Relapsed/Refractory NK/T-cell Lymphoma

TypeinterventionalSponsorShanghai Zhongshan HospitalRan2022 to 2024Enrolled40ConditionsNK/T Cell Lymphoma NosArmsBrentuximab Vedotin in Combination with Tislelizumab
3 · Its place in the literature

Who cites it

127 citing papers in PubMed.

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  8. Outcomes of patients treated with SVILECancer biology & medicine · 2020
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  18. The Significance of the Microenvironment in T/Nk-Cell Neoplasms.International journal of molecular sciences · 2025
    Review
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67 more citing papers are in PubMed but not listed here.

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

18 authors.

Xin LiDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Yasong ChengDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Mingzhi ZhangDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China. mingzhi_zhang1@126.com.
Jiaqin YanDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Ling LiDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Xiaorui FuDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Xudong ZhangDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Yu ChangDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Zhenchang SunDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Hui YuDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Lei ZhangDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Xinhua WangDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Jingjing WuDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Zhaoming LiDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Feifei NanDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Li TianDepartment of Oncology, Zhengzhou University First Affiliated Hospital; Lymphoma Diagnosis and Treatment Center of Henan Province, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Wencai LiDepartment of Pathology, Zhengzhou University First Affiliated Hospital, Νo. 1 Jianshe East Road, Zhengzhou, Henan, China.
Ken H YoungDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer/T-cell lymphoma (NKTCL) is a rare subtype of non-Hodgkin lymphoma that is associated with a poor outcome. Currently, the treatment needs of NKTCL remain unmet, and efforts to further improve treatment are urgently needed. Herein, seven patients with NKTCL who failed to respond to various types of chemotherapies were treated with the anti-programmed death 1 (anti-PD-1) antibody pembrolizumab at 100 mg every 3 weeks. After a median of four cycles of treatment (range 2-18), four out of seven patients responded (two complete response, two partial response, overall response rate 57%). Expression of PD1-ligand available was 50, 20, 30, 70, and 30% of five patients respectively. It is negative in one patient and not tested in one patient. Adverse events, which mostly ranged from grade I to grade III, were tolerable and could be safely handled, although immune-related pneumonitis was notable. Overall, PD-1 blockade with pembrolizumab represents a favorable strategy for the treatment of refractory/relapsed NKTCL.

Indexed as

AdultAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenFemaleHumansLymphoma, Extranodal NK-T-CellMaleMiddle AgedNeoplasm Recurrence, LocalTreatment OutcomeAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenpembrolizumabNK/T-cell lymphomaPD-1 blockadePembrolizumab

Identifiers

PMID29386072
PMCPMC5793390

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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.