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Poster Display

338P - Multicenter real-world study of advanced-stage non-nasal type NK/T cell lymphoma (NKTCL): Clinical features, treatment and prognosis

Date

02 Dec 2023

Session

Poster Display

Presenters

Yuce Wei

Citation

Annals of Oncology (2023) 34 (suppl_4): S1599-S1606. 10.1016/annonc/annonc1384

Authors

Y. Wei1, W. Liu2, F. Qi3, C. Zhang1, B. Zheng2, Y. Xie3, C. Bo4, D. Zhang1, W. Liu3, H. Fang4, Y. Chai1, S. Qi4, Y. Li4, W. Wang2, Y. Song3, J. Zhu3, M. Dong1

Author affiliations

  • 1 Medical Oncology, National Cancer Center / National Clinical Research Center for Cancer / Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, 100021 - Beijing/CN
  • 2 Radiation Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education / Beijing), Peking University Cancer Hospital & Institute, 100142 - Beijing/CN
  • 3 Lymphoma, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education / Beijing), Peking University Cancer Hospital & Institute, 100142 - Beijing/CN
  • 4 Radiation Oncology, National Cancer Center / National Clinical Research Center for Cancer / Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, 100021 - Beijing/CN

Resources

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Abstract 338P

Background

Nasal type NKTCL refers to upper aerodigestive tract (UAT) involvement while non-nasal type does not involve UAT at initial diagnosis. Since NKTCLs are predominantly nasal type, there remains little knowledge of non-nasal type disease.

Methods

Newly diagnosed advanced-stage non-nasal and nasal type NKTCL patients from two large cancer centers in the past 10-15 years were retrospectively collected.

Results

The study included 56 non-nasal type NKTCL patients with 139 nasal cases as controls. The non-nasal type NKTCLs exhibited higher Ki-67 expression levels compared to nasal cases (P=0.011) with no significant differences in other baseline features. With a median follow-up of 75.03 months, the non-nasal group showed slightly inferior overall survival (OS) compared to the nasal group (median OS [mOS]: 14.57 vs. 21.53 months, P=0.120). ECOG score≥2 (hazard ratio [HR]=2.18, P=0.039) and LDH elevation (HR=2.44, P=0.012) were correlated with worse OS, and the modified nomogram-revised risk index (NRI) and international prognostic index (IPI) functioned effectively for prognostic stratification. Multi- compared to single-modality therapy led to significantly superior progression-free survival (PFS) and OS (median PFS [mPFS]: 11.53 vs. 2.03 months, P=0.001; mOS: 52.80 vs. 7.70 months, P=0.006). Chemoradiotherapy combination significantly improved survival compared to other modalities (mPFS: 14.00 vs. 3.47 months, P=0.050; mOS: 56.40 vs. 9.30 months, P=0.046), and gemcitabine- compared to non-gemcitabine-based regimens showed a trend towards slightly improved outcomes (mPFS: 10.43 vs. 3.40 months, P=0.106; mOS: 25.13 vs. 9.30 months, P=0.125). Table: 338P

Prognostic stratification of advanced-stage non-nasal type ENKTLs

Model Variable Risk stratification Score Non-nasal type (n=56) (%) Nasal type (n=139) (%)
Modified NRI Age (>60 vs. ≤60 years)ECOG score (≥2 vs. 0-1) Elevated LDH (yes vs. no) low risk 0 16(28.6) 46(33.1)
high risk 1 30(53.6) 71(51.1)
2 5(8.9) 20(14.4)
3 5(8.9) 2(1.4)
Modified PINK Age (>60 vs. ≤60 years) Non-nasal type (yes vs. no) / 0 0 121(87.1)
1 45(80.4) 18(12.9)
2 11(19.6) 0
Modified IPI Age (>60 vs. ≤60 years)ECOG score (≥2 vs. 0-1)Elevated LDH (yes vs. no)Extranodal involvement (≥2 vs. 0-1) low risk 0 2(3.6) 6(4.3)
1 16(28.6) 46(33.1)
high risk 2 28(50.0) 66(47.5)
3 5(8.9) 19(13.7)
4 5(8.9) 2(1.4)

Conclusions

Advanced-stage non-nasal type NKTCL patients could achieve comparable prognosis with nasal cases after rational comprehensive therapy. Potent therapy is preferred in young patients with previously untreated disease, good performance status, and relatively low tumor burden.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Chinese Geriatric Oncology Society Scientific Research Fund (CGOS-06-2014-1-1-01600).

Disclosure

All authors have declared no conflicts of interest.

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