Evidence map›Paper›PMID 36626583›Full record

Trial reportBlood2023

Polatuzumab vedotin in previously untreated DLBCL: an Asia subpopulation analysis from the phase 3 POLARIX trial.

Yuqin Song, Hervé Tilly, Shinya Rai, Huilai Zhang, Jie Jin, Hideki Goto, Yasuhito Terui, Ho-Jin Shin, Won Seog Kim, Junning Cao and 21 more

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Blood, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03274492 (A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Comparing the Efficacy and Safety of Polatuzumab Vedotin in Combination With Rituximab and CHP), which is not on this map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
10.7field-weighted citation impact, top 1% 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.

NCT03274492 phase3completednot on this map

A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Comparing the Efficacy and Safety of Polatuzumab Vedotin in Combination With Rituximab and CHP (R-CHP) Versus Rituximab and CHOP (R-CHOP) in Previously Untreated Patients With Diffuse Large B-Cell Lymphoma

TypeinterventionalSponsorHoffmann-La RocheRan2017 to 2026Enrolled1,000ConditionsDiffuse Large B-Cell LymphomaArmsPolatuzumab Vedotin, Rituximab, Cyclophosphamide, Doxorubicin, Vincristine
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Five-Year Outcomes of the POLARIX Study Comparing Pola-R-CHP and R-CHOP in Patients With Diffuse Large B-Cell Lymphoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Trial
  4. Review
  5. Heterogeneity in primary gastrointestinal DLBCL: from clinical management to molecular mechanisms and treatment strategies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Observational
  13. Article
  14. Article
  15. Cell-of-Origin Subtype Predicts Response to Polatuzumab Vedotin in Large B-cell Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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

31 authors at 20 institutions in 7 countries.

Yuqin SongKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Beijing, China.
Hervé TillyCentre Henri Becquerel and University of Rouen, Rouen, France.
Shinya RaiKindai University Hospital, Osaka, Japan.ORCID 0000-0003-3929-9751
Huilai ZhangDepartment of Lymphoma, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin, China.
Jie JinThe First Affiliated Hospital of College of Medicine, Zhejiang University, Zhejiang, China.
Hideki GotoDepartment of Hematology, Hokkaido University Hospital, Sapporo, Japan.
Yasuhito TeruiThe Cancer Institute Hospital of JFCR, Tokyo, Japan.
Ho-Jin ShinPusan National University Hospital, Busan, Republic of Korea.
Won Seog KimSungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Republic of Korea.
Junning CaoFudan University Shanghai Cancer Center, Shanghai, China.
Jifeng FengJiangsu Cancer Hospital, Nanjing, China.
Hyeon Seok EomCenter for Hematologic Malignancy, National Cancer Center, Goyang, Republic of Korea.ORCID 0000-0002-0484-2067
Tae Min KimSeoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0001-6145-4426
Xavier Cheng-Hong TsaiNational Taiwan University Hospital, Taipei, Taiwan.ORCID 0000-0002-4174-8766
Jyh-Pyng GauTaipei Veterans General Hospital, Taipei, Taiwan.
Hideo KohDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Liling ZhangUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yongping SongDepartment of Hematology, Cancer Hospital Affiliated to Zhengzhou University, Zhengzhou, China.
Yu YangDepartment of Lymphoma, Head and Neck Oncology, Fujian Cancer Hospital, Fuzhou, China.
Wei LiDepartment of Hematology and Oncology, The First Hospital of Jilin University, Jilin, China.
He HuangDepartment of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Kiyoshi AndoDepartment of Hematology and Oncology, Tokai University School of Medicine, Isehara, Japan.
Jeff P SharmanWillamette Valley Cancer Institute/US Oncology, Eugene, OR.
Laurie H SehnBC Cancer Centre for Lymphoid Cancer and The University of British Columbia, Vancouver, BC, Canada.
Lilian BuF. Hoffmann-La Roche Ltd, Shanghai, China.
Xin WangF. Hoffmann-La Roche Ltd, Shanghai, China.
Yanwen JiangGenentech, Inc, South San Francisco, CA.
Jamie HirataGenentech, Inc, South San Francisco, CA.
Calvin LeeGenentech, Inc, South San Francisco, CA.ORCID 0000-0003-0716-8925
Jun ZhuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Beijing, China.
Koji IzutsuNational Cancer Center Hospital, Tokyo, Japan.
Amgen (United States) · USPeking University · CNRoche (China) · CNBusan National University of Education · KRCentre Henri BecquerelFirst Affiliated Hospital Zhejiang University · CNFudan University Shanghai Cancer Center · CNFujian Provincial Cancer Hospital · CNHokkaido University Hospital · JPJiangsu Cancer Hospital · CNJilin University · CNKindai University Hospital · JPNational Cancer Center · KRNational Taiwan University Hospital · TWOsaka Metropolitan University · JPSamsung Medical Center · KRSeoul National University Hospital · KRSun Yat-sen University · CNTaipei Veterans General Hospital · TWThe Cancer Institute Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the phase 3 POLARIX study in previously untreated diffuse large B-cell lymphoma, polatuzumab vedotin combined with rituximab plus cyclophosphamide, doxorubicin, and prednisone (Pola-R-CHP) significantly improved progression-free survival (PFS) compared with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) with similar safety. Patients were randomized 1:1 to 6 cycles of Pola-R-CHP or R-CHOP plus 2 cycles of rituximab alone. For registration of POLARIX in China, consistency of PFS in an Asia subpopulation (defined as ≥50% of the risk reduction in PFS expected in the global population) was evaluated. Overall, 281 patients were analyzed: 160 patients from Asia in the intention-to-treat (ITT) population of the global study and 121 from an ITT China extension cohort. Of these, 141 were randomized to Pola-R-CHP and 140 to R-CHOP. At data cutoff (28 June 2021; median follow-up 24.2 months), PFS met the consistency definition with the global population, and was superior with Pola-R-CHP vs R-CHOP (hazard ratio, 0.64; 95% confidence interval [CI], 0.40-1.03). Two-year PFS was 74.2% (95% CI, 65.7-82.7) and 66.5% (95% CI, 57.3-75.6) with Pola-R-CHP and R-CHOP, respectively. Safety was comparable between Pola-R-CHP and R-CHOP, including rates of grade 3 to 4 adverse events (AEs; 72.9% vs 66.2%, respectively), serious AEs (32.9% vs 32.4%), grade 5 AEs (1.4% vs 0.7%), AEs leading to study treatment discontinuation (5.0% vs 7.2%), and any-grade peripheral neuropathy (44.3% vs 50.4%). These findings demonstrate consistent efficacy and safety of Pola-R-CHP vs R-CHOP in the Asia and global populations in POLARIX. This trial was registered at https://clinicaltrials.gov/ct2/home as # NCT03274492.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLymphoma, Large B-Cell, DiffuseAntibodies, MonoclonalCyclophosphamideDoxorubicinHumansImmunoconjugatesPrednisoneRituximabVincristineAntibodies, MonoclonalCyclophosphamideDoxorubicinImmunoconjugatespolatuzumab vedotinPrednisoneRituximabVincristine

Identifiers

PMID36626583
PMCPMC10646777
OpenAlexW4315473447

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.