Monitoring early responses to neoadjuvant chemotherapy and the factors affecting neoadjuvant chemotherapy responses in primary osteosarcoma

被引:1
|
作者
Yu, Hong [1 ]
Gao, Lei [1 ]
Shi, Ruiqing [1 ]
Kong, Mengjuan [2 ]
Duan, Lisha [1 ]
Cui, Jianling [1 ,3 ]
机构
[1] Hosp Hebei Med Univ 3, Dept Radiol, Shijiazhuang, Peoples R China
[2] Tianjin Univ Tianjin Hosp, Dept Radiol, Tianjin, Peoples R China
[3] Hosp Hebei Med Univ 3, Dept Radiol, 139 Ziqiang Rd, Shijiazhuang 050050, Peoples R China
关键词
Conventional osteosarcoma; diffusion-weighted imaging; neoadjuvant chemotherapy; necrosis rate; SARCOMA;
D O I
10.21037/qims-22-1095
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: This study sought to predict the early responses to neoadjuvant chemotherapy (NACT) of patients with primary conventional osteosarcoma (COS) using the apparent diffusion coefficient (ADC) and to evaluate the factors affecting the tumor necrosis rate (TNR).Methods: The data of 41 patients who underwent magnetic resonance imaging (MRI) and diffusion-weighted imaging sequence scans before NACT, 5 days after the end of the first phase of NACT, after the end of the whole course of chemotherapy, were prospectively collected. ADC1 refers to the ADC before chemotherapy, ADC2 refers to the ADC after the first phase of chemotherapy, and ADC3 refers to the ADC before surgery. The change in values before and after the first phase of chemotherapy was calculated as follows: ADC2-1 = ADC2 - ADC1. The change in values before and after the last phase of chemotherapy was calculated as follows: ADC3-1 = ADC3 - ADC1. The change in values after the first phase and the last phase of chemotherapy was calculated as follows: ADC3-2 = ADC3 - ADC2. We recorded the patient characteristics, including age, gender, pulmonary metastasis, alkaline phosphatase (ALP), and lactate dehydrogenase (LDH). The patients were divided into the following 2 groups based on their histological TNR after postoperative: (I) the good-response group (>= 90% necrosis, n=13) and (II) the poor-response group (<90% necrosis, n=28). Changes in the ADCs were compared between the good-response and poor-response groups. The different ADCs between the 2 groups were compared, and a receiver operating characteristic analysis was performed. A correlation analysis was performed to assess the correlations of the clinical features, laboratory features, and different ADCs with patients' histopathological responses to NACT.Results: The ADC2 (P<0.001), ADC3 (P=0.004), ADC3-1 (P=0.008), ADC3-2 (P=0.047), and ALP before NACT (P=0.019) were significantly higher in the good-response group than in the poor-response group. The ADC2 [area under the curve (AUC) =0.723; P=0.023), ADC3 (AUC =0.747; P=0.012), and ADC3-1 (AUC =0.761; P=0.008) showed good diagnostic performance. Based on the univariate binary logistic regression analysis, the ADC2 (P=0.022), ADC3 (P=0.009), ADC2-1 (P=0.041), and ADC3-1 (P=0.014) were correlated with the TNR. However, based on the multivariate analysis, these parameters were not significantly correlated with the TNR. Conclusions: In patients with COS who are undergoing neoadjuvant chemotherapy, the ADC2 is a promisingindicator for predicting tumor response to chemotherapy in early.
引用
收藏
页码:3716 / 3725
页数:10
相关论文
共 50 条
  • [1] DISPARATE HISTOLOGIC RESPONSES IN SIMULTANEOUSLY RESECTED PRIMARY AND METASTATIC OSTEOSARCOMA FOLLOWING INTRAVENOUS NEOADJUVANT CHEMOTHERAPY
    NACHMAN, J
    SIMON, MA
    DEAN, L
    SHERMETA, D
    DAWSON, P
    VOGELZANG, NJ
    JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (08) : 1185 - 1190
  • [2] YReal World Responses to Neoadjuvant Chemotherapy for Early Breast Cancer
    Merrick, S.
    Yu, T.
    Papadimitraki, E.
    CLINICAL ONCOLOGY, 2022, 34 (04) : E176 - E176
  • [3] NEOADJUVANT CHEMOTHERAPY FOR OSTEOSARCOMA OF THE EXTREMITY
    BACCI, G
    SPRINGFIELD, D
    CAPANNA, R
    PICCI, P
    GUERRA, A
    ALBISSINI, U
    RUGGIERI, P
    BIAGINI, R
    CAMPANACCI, M
    CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 1987, (224) : 268 - 276
  • [4] NEOADJUVANT CHEMOTHERAPY FOR OSTEOSARCOMA IN CHILDREN
    SASAKI, K
    CANCER CHEMOTHERAPY : CHALLENGES FOR THE FUTURE, VOL 4, 1989, 904 : 195 - 199
  • [5] Neoadjuvant chemotherapy for pediatric osteosarcoma patients
    Uchida, A
    Myoui, A
    Araki, N
    Yoshikawa, H
    Shinto, Y
    Ueda, T
    CANCER, 1997, 79 (02) : 411 - 415
  • [6] Clinical evaluation of neoadjuvant chemotherapy for osteosarcoma
    Zhu, Wengang
    Zhu, Lizhen
    Bao, Yongzheng
    Zhong, Xueren
    Chen, Yu
    Wu, Qiang
    JOURNAL OF BUON, 2019, 24 (03): : 1181 - 1185
  • [7] NEOADJUVANT CHEMOTHERAPY FOR NONMETASTATIC OSTEOSARCOMA OF THE EXTREMITIES
    BACCI, G
    PICCI, P
    PIGNATTI, G
    DECRISTOFARO, R
    DALLARI, D
    AVELLA, M
    MANFRINI, M
    MARANGOLO, M
    FERRUZZI, A
    MERCURI, M
    RUGGIERI, P
    BIAGINI, R
    CAPANNA, R
    FERRARI, S
    PRASAD, R
    CAMPANACCI, M
    CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 1991, (270) : 87 - 98
  • [8] Analysis of prognostic factors and histopathological response to neoadjuvant chemotherapy in osteosarcoma
    Erdogan, Furkan
    Cinka, Hikmet
    Akman, Bahattin Cagdas
    Coskun, Huseyin Sina
    Dabak, Nevzat
    JOINT DISEASES AND RELATED SURGERY, 2023, 34 (01): : 196 - 206
  • [9] Adjuvant and Neoadjuvant Chemotherapy for Osteosarcoma: A Historical Perspective
    Benjamin, Robert S.
    CURRENT ADVANCES IN OSTEOSARCOMA: CLINICAL PERSPECTIVES: PAST, PRESENT AND FUTURE, 2ND EDITION, 2020, 1257 : 1 - 10
  • [10] Different Responses to Neoadjuvant Chemotherapy in Urothelial Carcinoma Molecular Subtypes
    Sjodahl, Gottfrid
    Abrahamsson, Johan
    Holmsten, Karin
    Bernardo, Carina
    Chebil, Gunilla
    Eriksson, Pontus
    Johansson, Iva
    Kollberg, Petter
    Lindh, Claes
    Lovgren, Kristina
    Marzouka, Nour-al-Dain
    Olsson, Hans
    Hoglund, Mattias
    Ullen, Anders
    Liedberg, Fredrik
    EUROPEAN UROLOGY, 2022, 81 (05) : 523 - 532