Influence of Tumor Cavitation on Assessing the Clinical Benefit of Anti-PD1 or PD-L1 Inhibitors in Advanced Lung Squamous Cell Carcinoma

被引:2
|
作者
Chen, Qin [1 ,2 ,3 ,4 ]
Wang, Jing [1 ,2 ,3 ]
Wang, Xinyue [1 ,2 ,3 ]
Yin, Yan [4 ]
Wang, Xuan [5 ]
Song, Zhenchun [6 ]
Xing, Bin [4 ]
Li, Yajing [4 ]
Zhang, Jingjing [4 ]
Qin, Jianwen [4 ]
Jiang, Richeng [1 ,2 ,3 ,6 ,7 ,8 ]
机构
[1] Tianjin Med Univ, Tianjin Canc Inst & Hosp, Tianjin Lung Canc Ctr, Dept Thorac Oncol, Huanhu West Rd, Tianjin 300060, Peoples R China
[2] Natl Clin Res Ctr Canc, Tianjin Key Lab Canc Prevent & Therapy, Tianjin, Peoples R China
[3] Tianjins Clin Res Ctr Canc, Tianjin, Peoples R China
[4] Tianjin Chest Hosp, Dept Resp & Crit Med, Taierzhuang South Rd, Tianjin 300222, Peoples R China
[5] Tianjin Med Univ, Tianjin Huanhu Hosp, Dept Neurosurg, Tianjin, Peoples R China
[6] Tianjin Chest Hosp, Med Radiol Dept, Tianjin, Peoples R China
[7] Tianjin Canc Hosp Airport Hosp, Canc Precise Diag Ctr, Tianjin, Peoples R China
[8] Tianjin Med Univ Canc Inst & Hosp, Ctr Precis Canc Med & Translat Res, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
Immunotherapy; Lung squamous cell cancer; mRECIST; RECIST; 1.1; RESPONSE EVALUATION CRITERIA; SOLID TUMORS; CANCER; PEMBROLIZUMAB; THERAPY; HEMOPTYSIS; MRECIST; PSEUDOPROGRESSION; REPRODUCIBILITY; IMMUNOTHERAPY;
D O I
10.1016/j.cllc.2023.10.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A significant portion of lung squamous cell cancer (LUSC) shows radiographic signs of cavitation, which is not considered in current RECIST v1.1 or iRECIST guidelines. We reviewed radiologic data of 785 stage IV LUSC patients treated with PD-1/PD-L1 antibodies combined with platinum-based doublet chemotherapy. 131 patients exhibited cavitation lesions pre- or after-treatment. The response was assessed both by RECIST v1.1 and mRECIST. Survival curves for different response categories were prepared using Kaplan-Meier and log-rank tests. Weighted kappa statistics were used to assess interobserver reproducibility. We found that traditional testing methods have underestimated the benefits of immunotherapy in 9.2% of LUSC patients with tumor cavitation. mRECIST assessment resulted in a higher response rate than RECIST v1.1 (66% versus 57%) and better identified patients with PFS and OS benefits due to cavitation. The interobserver reproducibility of mRECIST for tumor cavitation evaluation was acceptable (0.821). mRECIST measurement of target lesions incorporating cavitation assessment provides better size change discrimination than measuring the external diameter alone, offering a feasible and robust method for response evaluation and predicting patient benefits. These results may inform further modifications to RECIST V1.1 to better reflect efficacy with immunotherapy. Purpose: A considerable portion of lung squamous cell cancer (LUSC) displays radiographic signs of cavitation. The cavitation of lesions is not accounted for in the prevailing Evaluation Criteria of Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 or iRECIST in lung cancer. We hypothesized that cavitation might alter response assessment in these patients. Patients and Methods: We performed a retrospective radiologic review of 785 patients with stage IV LUSC treated with PD-1/PD-L1 antibody combined with platinum-based doublet chemotherapy. 131 patients exhibited cavitation lesions pre- or after-treatment. Response was assessed by RECIST v1.1 and a modified Evaluation Criteria in Solid Tumors (mRECIST) guidelines in which the longest diameter of any cavity was subtracted from the overall longest diameter of that lesion to measure target lesions. The response rate and PFS and OS between mRECIST and RECIST v1.1 were compared. Survival curves of different response categories in each criterion were prepared using the method of Kaplan-Meier and log-rank tests. Weighted kappa statistics were used to assess interobserver reproducibilities and to compare response rates. The chi-square test confirmed the relationship between PD-L1 expression and posttreatment cavitation. Results: Notable cavitation of pulmonary lesions was seen in 16.7% of 785 patients treated with immunotherapy combined with platinum-based chemotherapy. Using the mRECIST for response assessment resulted in a higher response rate than RECIST v1.1 (66% vs. 57%). mRECIST might better identify patients with PFS and OS benefits who have cavitation. The chi-square test revealed a marginally significant difference between PD-L1 expression and tumor cavitation. Interobserver reproducibility of mRECIST for tumor cavitation evaluation was acceptable (the weighted k coefficients for mRECIST criteria was 0.821). Conclusion: Cavitation lesions at baseline and after checkpoint treatment are common in LUSC patients. mRECIST records a significantly higher response rate than RECIST for these LUSC patients. Response assessment might be improved by incorporating cavitation into volume assessment for target lesions. These results may inform further modifications to RECIST V1.1 to better reflect efficacy with immunotherapy
引用
收藏
页码:29 / 38
页数:10
相关论文
共 50 条
  • [31] Datasets for gene expression profiles of head and neck squamous cell carcinoma and lung cancer treated or not by PD1/PD-L1 inhibitors
    Foy, Jean-Philippe
    Karabajakian, Andy
    Ortiz-Cuaran, Sandra
    Boussageon, Maxime
    Michon, Lucas
    Bouaoud, Jebrane
    Fekiri, Dorssafe
    Robert, Marie
    Baffert, Kim-Arthur
    Herve, Genevieve
    Quilhot, Pauline
    Attignon, Valery
    Girod, Angelique
    Chaine, Andre
    Benassarou, Mourad
    Zrounba, Philippe
    Caux, Christophe
    Ghiringhelli, Francois
    Lantuejoul, Sylvie
    Crozes, Carole
    Brocheriou, Isabelle
    Perol, Maurice
    Fayette, Jerome
    Bertolus, Chloe
    Saintigny, Pierre
    DATA IN BRIEF, 2022, 44
  • [32] PD-L1 expression in squamous cell lung carcinoma in small biopsy specimens
    Dzambas, J.
    Aleksic, I.
    VIRCHOWS ARCHIV, 2021, 479 (SUPPL 1) : S52 - S53
  • [33] The Expression of PD-L1 Protein as a Prognostic Factor in Lung Squamous Cell Carcinoma
    Takada, K.
    Okamoto, T.
    Toyokawa, G.
    Kozuma, Y.
    Matsubara, T.
    Haratake, N.
    Akamine, T.
    Takamori, S.
    Katsura, M.
    Shoji, F.
    Oda, Y.
    Maehara, Y.
    JOURNAL OF THORACIC ONCOLOGY, 2017, 12 (11) : S1994 - S1994
  • [34] Model combining genomic and clinical factors to predict clinical benefit from PD1/PD-L1 inhibitors for advanced UC
    Nassar, Amin
    Mouw, Kent William
    Liu, Chia-Jen
    Lundgren, Kevin
    Van Allen, Eliezer Mendel
    Harshman, Lauren Christine
    Pomerantz, Mark
    Preston, Mark A.
    Wei, Xiao X.
    McGregor, Bradley Alexander
    Choudhury, Atish Dipankar
    Bellmunt, Joaquim
    Choueiri, Toni K.
    Kwiatkowski, David J.
    Sonpavde, Guru
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
  • [35] Anti-PD1/PD-L1 Immunotherapy for Non-Small Cell Lung Cancer with Actionable Oncogenic Driver Mutations
    Dantoing, Edouard
    Piton, Nicolas
    Salaun, Mathieu
    Thiberville, Luc
    Guisier, Florian
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (12)
  • [36] Optimal Selection of Patients with Genitourinary Cancers for Anti-PD1/PD-L1 Treatment with a Focus on Urothelial and Renal Cell Carcinoma
    Zeuschner, Philip
    Junker, Kerstin
    EUROPEAN UROLOGY FOCUS, 2022, 8 (04): : 907 - 909
  • [37] Clinical relevance of PD-L1 and PD-L2 overexpression in patients with esophageal squamous cell carcinoma
    Hsieh, Chih-Cheng
    Hsu, Han-Shui
    Li, Anna Fen-Yau
    Chen, Yann-Jang
    JOURNAL OF THORACIC DISEASE, 2018, 10 (07) : 4433 - 4444
  • [38] Germinal immunogenetics as a predictor of anti-PD1/PD-L1 treatment outcome.
    Milano, Gerard A.
    Refae, Sadal
    Ebran, Nathalie
    Gal, Jocelyn
    Otto, Josiane
    Drubay, Damien
    Chamorey, Emmanuel
    Ciccolini, Joseph
    Saada, Esma
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
  • [39] PD-1/PD-L1 Checkpoint Inhibitors in Tumor Immunotherapy
    Liu, Jinhua
    Chen, Zichao
    Li, Yaqun
    Zhao, Wenjie
    Wu, JiBiao
    Zhang, Zhen
    FRONTIERS IN PHARMACOLOGY, 2021, 12
  • [40] Mild hyperthermia upregulates PD-L1 in the tumor microenvironment and enhances antitumor efficacy of PD-L1 blockade in murine squamous cell carcinoma
    Ohta, Yuya
    Ichimura, Norihisa
    Yamaguchi, Satoshi
    Ohara, Go
    Yamamoto, Noriyuki
    Itoh, Yoshiyuki
    Yamada, Keiichiro
    Nakamura, Seiji
    Hibi, Hideharu
    NAGOYA JOURNAL OF MEDICAL SCIENCE, 2024, 86 (03): : 497 - 506