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JCI Insight. 2023;8(2):164767.

Chemotherapy delivery time affects treatment outcomes of female patients with diffuse large B cell lymphoma.

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제1저자 김대욱, 변자민 · 교신저자 고영일, 김재영

소속 (4)
  1. Department of Mathematical Sciences, KAIST, Daejeon, South Korea.
  2. Biomedical Mathematics Group, Institute for Basic Science, Daejeon, South Korea.
  3. Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, South Korea.
  4. Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, South Korea.

Abstract

BACKGROUNDChronotherapy is a drug intervention at specific times of the day to optimize efficacy and minimize adverse effects. Its value in hematologic malignancy remains to be explored, in particular in adult patients.METHODSWe performed chronotherapeutic analysis using 2 cohorts of patients with diffuse large B cell lymphoma (DLBCL) undergoing chemotherapy with a dichotomized schedule (morning or afternoon). The effect of a morning or afternoon schedule of rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) on survival and drug tolerability was evaluated in a survival cohort (n = 210) and an adverse event cohort (n = 129), respectively. Analysis of about 14,000 healthy individuals followed to identify the circadian variation in hematologic parameters.RESULTSBoth progression-free survival (PFS) and overall survival (OS) of female, but not male, patients were significantly shorter when patients received chemotherapy mostly in the morning (PFS HR 0.357, P = 0.033; and OS HR 0.141, P = 0.032). The dose intensity was reduced in female patients treated in the morning (cyclophosphamide 10%, P = 0.002; doxorubicin 8%, P = 0.002; and rituximab 7%, P = 0.003). This was mainly attributable to infection and neutropenic fever: female patients treated in the morning had a higher incidence of infections (16.7% vs. 2.4%) and febrile neutropenia (20.8% vs. 9.8%) as compared with those treated in the afternoon. The sex-specific chronotherapeutic effects can be explained by the larger daily fluctuation of circulating leukocytes and neutrophils in female than in male patients.CONCLUSIONIn female DLBCL patients, R-CHOP treatment in the afternoon can reduce toxicity while it improves efficacy and survival outcome.FUNDINGNational Research Foundation of Korea (NRF) grant funded by the Korean government (grant number NRF-2021R1A4A2001553), Institute for Basic Science IBS-R029-C3, and Human Frontiers Science Program Organization Grant RGY0063/2017.

Keywords

CancerCancer immunotherapyHematologyLymphomasOncology

Figures

Figure 1
Figure 1 CONSORT diagram describing the flow of patient enrollment. Peg, pegylated; CR, complete remission; ANC, absolute neutrophil count; Hb, hemoglobin.
Figure 2
Figure 2 Kaplan-Meier curves of PFS and OS according to the time of the day of R-CHOP delivery and sex. (A) The procedure of R-CHOP chemotherapy. (B–G) PFS of MG and AG (B), female MG and AG (C), and male MG and AG (D) and OS of MG and AG (E), female MG and AG (F), and male MG and AG (G). Cross (+) indicates censoring of data. Here, 210 patients in the survival cohort were analyzed. P values were calculated by log-rank test.
Figure 3
Figure 3 Even after adjusting for R-IPI, PFS and OS decrease more rapidly in the female MG than in the female AG. (A–F) Cox proportional-hazard survival curves of PFS (A–C) and OS (D–F) according to sex and time of the day of R-CHOP delivery after adjusting for R-IPI (Supplemental Figure 1). PFS of MG and AG (A), female MG and AG (B), and male MG and AG (C) and OS of MG and AG (D), female MG and AG (E), and male MG and AG (F). PFS (A) and OS (D) are not different between MG and AG. However, PFS (B) and OS (E) are different between the female MG and AG: they decrease more rapidly in the female MG than in the female AG. In contrast, there is no difference between the male MG and AG (C and F). Here, 210 patients in the survival cohort were analyzed. P values were calculated by Wald’s test.
Figure 4
Figure 4 Dose intensity of cyclophosphamide, doxorubicin, rituximab, and vincristine according to sex and the time of the day of R-CHOP delivery. (A) The definition of dose intensity (DI), planned dose intensity (PDI), and relative dose intensity (RDI). (B–E) RDI of cyclophosphamide (B), doxorubicin (C), rituximab (D), and vincristine (E) in MG and AG, female MG and AG, and male MG and AG. (F–I) The fraction of patients receiving less than 80% of PDI of cyclophosphamide (F), doxorubicin (G), rituximab (H), and vincristine (I) in MG and AG, female MG and AG, and male MG and AG. Here, 129 patients in the adverse event cohort were analyzed. P values in B–E and those in F–I were calculated by Mann-Whitney U test and χ2 test, respectively. Error bar denotes IQR. *P < 0.05; **P < 0.01.
Figure 5
Figure 5 WBC, ANC, Hb, and platelet abundance according to sex and time of the day of measurement. Here, box-and-whisker graphs describing the distribution of the hematology parameters were plotted. The outliers that are defined to be outside 1.5 times IQR either above the upper quartile or below the lower quartile are denoted by circles. Lines within boxes represent medians. The sample numbers of WBC (A), ANC (B), Hb (C), and platelet (D) abundance are 6,447, 6,720, 6,736, and 6,882 in the female group and 7,728, 7,891, 7,246, and 7,916 in the male group, respectively. P values were calculated by Mann-Whitney U test. ***P < 0.001.

그림 출처: PubMed Central 공개 논문 (PMC9977288)

그 밖의 정보
출판 형태
Journal Article
저널
JCI insight · eISSN 2379-3708
전자 출판
2023-01-24
MeSH
Adult · Male · Humans · Female · Rituximab / therapeutic use · Antibodies, Monoclonal, Murine-Derived / adverse effects · Antineoplastic Combined Chemotherapy Protocols* / therapeutic use · Treatment Outcome · Lymphoma, Large B-Cell, Diffuse* / therapy · Vincristine · Cyclophosphamide · Prednisone · Doxorubicin
Substances
Rituximab · Antibodies, Monoclonal, Murine-Derived · Vincristine · Cyclophosphamide · Prednisone · Doxorubicin
참고문헌
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