Evidence map›Paper›PMID 37675232›Full record

ArticleFrontiers in oncology2023

Comparison of first-line treatment with CHOP versus ICED in patients with peripheral T-cell lymphoma eligible for upfront autologous stem cell transplantation.

Seok Jin Kim, Jae-Cheol Jo, Dok Hyun Yoon, Deok-Hwan Yang, Sang Eun Yoon, Gyeong-Won Lee, Jee Hyun Kong, Yong Park, Ka-Won Kang, Ho-Sup Lee and 16 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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.

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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
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

26 authors at 20 institutions in 1 country.

Seok Jin KimDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Jae-Cheol JoDepartment of Hematology and Oncology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Republic of Korea.
Dok Hyun YoonDepartment of Oncology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Deok-Hwan YangDepartment of Internal Medicine, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, Gwangju, Republic of Korea.
Sang Eun YoonDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Gyeong-Won LeeDivision of Hematology and Oncology, Department of Internal Medicine, Gyeongsang National University Hospital, Gyeongsang National University College of Medicine, Changwon, Republic of Korea.
Jee Hyun KongDepartment of Hematology-oncology, Division of Internal Medicine, Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea.
Yong ParkDepartment of Internal Medicine, Korea University College of Medicine, Korea University Anam Hospital, Seoul, Republic of Korea.
Ka-Won KangDepartment of Internal Medicine, Korea University College of Medicine, Korea University Anam Hospital, Seoul, Republic of Korea.
Ho-Sup LeeDepartment of Internal Medicine, Kosin University Gospel Hospital, Busan, Republic of Korea.
Sung Yong OhDepartment of Internal Medicine, Dong-A University Medical Center, Busan, Republic of Korea.
Ho-Jin ShinDepartment of Internal Medicine, Pusan National University Hospital, Busan, Republic of Korea.
Won Sik LeeDepartment of Internal Medicine, Inje University Busan Paik Hospital, Busan, Republic of Korea.
Yoon Seok ChoiDivision of Hematology-Oncology, Department of Internal Medicine, Ajou University School of Medicine, Suwon, Republic of Korea.
Seong Hyun JeongDivision of Hematology-Oncology, Department of Internal Medicine, Ajou University School of Medicine, Suwon, Republic of Korea.
Min Kyoung KimDepartment of Internal Medicine, Yeungnam University College of Medicine, Daegu, Republic of Korea.
Hye Jin KangDepartment of Internal Medicine, Korea Cancer Center Hospital, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
Jun Ho YiDepartment Internal Medicine, Chung-Ang University Hospital, Seoul, Republic of Korea.
Sung-Nam LimDepartment of Internal Medicine, Haeundae Baek Hospital, Busan, Republic of Korea.
Ho-Young YhimDepartment of Internal Medicine, Jeonbuk National University Medical School, Research Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital, Jeonju, Republic of Korea.
Young Rok DoDepartment of Internal Medicine, Dongsan Medical Center, Daegu, Republic of Korea.
Hwan Jung YunDepartment of Internal Medicine, Chungnam National University Hospital, Daejeon, Republic of Korea.
Hyeon-Seok EomHematology-Oncology Clinic, National Cancer Center, Go-Yang, Republic of Korea.
Mark Hong LeeDivision of Hematology-Oncology, Department of Internal Medicine, Konkuk University Medical Center, Seoul, Republic of Korea.
Cheolwon SuhDepartment of Oncology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Won Seog KimDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Ajou University · KRKorea University · KRSungkyunkwan University · KRAsan Medical Center · KRChonnam National University Hwasun Hospital · KRChung-Ang University Hospital · KRChungnam National University Hospital · KRDong-A University · KRGyeongsang National University Hospital · KRInje University Busan Paik Hospital · KRJeonbuk National University Hospital · KRKeimyung University · KRKonkuk University Medical Center · KRKorea Institute of Radiological and Medical Sciences · KRKosin University Gospel Hospital · KRNational Cancer Center · KRPusan National University Hospital · KRSamsung (South Korea) · KRUlsan College · KRUniversity of Ulsan · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Upfront autologous stem cell transplantation (ASCT) has been recommended for patients who are newly diagnosed with peripheral T-cell lymphoma (PTCL), and CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone), an anthracycline-based chemotherapy has been the frontline chemotherapy for PTCL. However, it is not clear whether anthracycline-based chemotherapies such as CHOP could be standard induction therapy for PTCL. Methods: We conducted a randomized phase II study to compare CHOP with fractionated ifosfamide, carboplatin, etoposide, and dexamethasone (ICED) for patients eligible for ASCT. The primary endpoint was progression-free survival (PFS) and secondary endpoints included objective response rate, overall survival (OS), and safety profiles. Results: Patients were randomized into either CHOP (n = 69) or ICED (n = 66), and the characteristics of both arms were not different. PTCL-not otherwise specified (NOS, n = 60) and angioimmunoblastic T-cell lymphoma (AITL, n = 53) were dominant. The objective response rate was not different between CHOP (59.4%) and ICED (56.1%), and the 3-year PFS was not different between CHOP (36.7%) and ICED (33.1%). In AITL patients, CHOP was favored over ICED whereas ICED was associated with more cytopenia and reduced dose intensity. Patients who received upfront ASCT after achieving complete response to CHOP or ICED showed 80% of 3-year OS. Discussion: In summary, our study showed no therapeutic difference between CHOP and ICED in terms of response and PFS. Thus, CHOP might remain the reference regimen especially for AITL based on its better outcome in AITL, and upfront ASCT could be recommended as a consolidation of complete response in patients with PTCL.

Indexed as

autologous stem cell transplantationchemotherapylymphomaprogression-free survivalT-cell

Identifiers

PMID37675232
PMCPMC10477982
OpenAlexW4386113198

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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.