Lactate dehydrogenase kinetics predict chemotherapy response in recurrent metastatic nasopharyngeal carcinoma

Author:

Huang Luo123,Sim Adelene Y. L.45,Wu Yongzhong2,Liang Zhongguo1,Li Kaiguo1,Du Youqin1,Ong Enya H. W.34,Tan Hong Qi34,Wee Joseph T. S.35,Xie Yue2,Shu Xiaolei2,Wang Ying6,Chua Melvin L. K.745ORCID,Zhu Xiaodong8

Affiliation:

1. Department of Radiation Oncology, Guangxi Medical University Cancer Hospital, Nanning, China

2. Department of Radiation Oncology, Chongqing University Cancer Hospital, Chongqing, China

3. Division of Radiation Oncology, National Cancer Centre Singapore, Singapore

4. Division of Medical Sciences, National Cancer Centre Singapore, Singapore

5. Oncology Academic Clinical Programme, Duke-NUS Medical School, Singapore

6. Department of Radiation Oncology, Chongqing University Cancer Hospital, 181 Han Yu Road, Chongqing, 400030, China

7. Division of Radiation Oncology, National Cancer Centre Singapore, 11 Hospital Crescent, Singapore, 169610, Singapore

8. Department of Radiation Oncology, Guangxi Medical University Cancer Hospital, 77 He Di Road, Nanning, 530021, China

Abstract

Background: Lactate dehydrogenase (LDH) is a known prognostic biomarker for the endemic variant of nasopharyngeal carcinoma (NPC). Here, we investigate whether serial changes in LDH level between chemotherapy (CT) cycles are associated with tumour response to CT. Methods: Patients with biopsy-proven, recurrent or treatment-naïve metastatic NPC (mNPC) were recruited. All patients had received at least two cycles of platinum-based doublet or triplet CT, with serial assessment of LDH prior to every cycle of chemotherapy (CT1–6). Patients harbouring conditions that affect LDH levels (IU/L) were excluded. Tumour response was assessed after every two cycles of CT by RECIST v1.1. Results: A total of 158 patients were analysed, including 77 with recurrent and 81 with treatment-naïve mNPC. High pre-CT LDH was associated with an inferior overall survival [hazard ratio 1.93 for ⩾240 versus <240 (1.34–2.77), p < 0.001], which is consistent with published literature. We found that both absolute LDH levels and LDH ratios (LDHCTn: LDHCTn–1) were associated with tumour response [partial response versus progressive disease: median value across CT1–6 = 168–190 versus 222–398 (absolute); 0.738–0.988 versus 1.039–1.406 (ratio)], albeit LDH ratio had a tighter variance between patients. Finally, we showed that an LDH ratio cut-off of 1.0 at CT1, CT3 and CT5 was predictive of progressive disease at CT2, CT4, CT6 [area under the curve of 0.73 (0.65–0.80)]. Conclusion: Herein, we characterised the longitudinal variation of LDH in response to CT in mNPC. Our findings suggest the potential utility of interval LDH ratio to predict subsequent tumour response to CT.

Funder

Chongqing Science and Technology Commission

National Medical Research Council

National Natural Science Foundation of China

Publisher

SAGE Publications

Subject

Oncology

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