Cargando…

氟达拉滨和环磷酰胺联合利妥昔单抗(FCR方案)一线治疗慢性淋巴细胞白血病43例临床分析

OBJECTIVE: To investigate the efficacy of fludarabine and cyclophosphamide combined with rituximab(FCR)in previously untreated patients with chronic lymphocytic leukemia(CLL). METHODS: The clinical data of 43 enrolled patients from May 2004 to December 2017 were analyzed the efficacy and survival re...

Descripción completa

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408492/
https://www.ncbi.nlm.nih.gov/pubmed/34455740
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.07.003
_version_ 1783746834684968960
collection PubMed
description OBJECTIVE: To investigate the efficacy of fludarabine and cyclophosphamide combined with rituximab(FCR)in previously untreated patients with chronic lymphocytic leukemia(CLL). METHODS: The clinical data of 43 enrolled patients from May 2004 to December 2017 were analyzed the efficacy and survival results. RESULTS: A total of 43 patients with 31 males and 12 females, and the median age was 58 years old(range 36 to72)before treatment. There were 8 patients with symptom B. The median number of peripheral blood lymphocyte was 26(3–550)×10(9)/L. IGHV unmutated was detected in 62.1%(18/29)patients, P53 deletion in 14%(6/43)patients, RB1 deletion in 18.6%(8/43)patients, Trisomy 12 in 25.6%(11/33)patients, ATM deletion in 16.7%(7/42)patients, respectively. The median number of treatment courses administered was 4(range 2–6). Twenty patients obtained CR(46.5%), 18 patients obtained PR, 4 patients were SD, 1 patient was PD. The overall response rate(ORR)was 88.37%. Seven patients obtained MRD negative. After the median follow-up time of 51(6–167)months, median PFS was 67(29–105)months, median OS was not reach, 5-year PFS was(62.1±8.6)%, 10-year PFS was(31±14.3)%, 5-year OS was(70.5±8.3)%, and 10-year OS was(51.3±13.8)%. Less than 4 courses predicted adverse OS(P<0.05). P53 deletion and less than 4 courses were associated with poor PFS(P<0.001),and the prognostic value still remained after multivariate analysis[HR=7.65(95%CI 1.74–33.60), P=0.007; HR=3.75(95% CI 1.19–11.80), P=0.025]. Eighteen patients(41.9%)appeared grade 2–3 infection after chemotherapy, and 19 patients(44.2%)appeared grade 3–4 hematological adverse reactions. One patient(2.3%)was developed tumor lysis syndrome. All adverse reactions were controlled or recovered spontaneously. CONCLUSION: Previously untreated CLL patients treated with FCR had a high response rate and good survival rate, which is an important treatment choice for fit patients.
format Online
Article
Text
id pubmed-8408492
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Editorial office of Chinese Journal of Hematology
record_format MEDLINE/PubMed
spelling pubmed-84084922021-09-15 氟达拉滨和环磷酰胺联合利妥昔单抗(FCR方案)一线治疗慢性淋巴细胞白血病43例临床分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To investigate the efficacy of fludarabine and cyclophosphamide combined with rituximab(FCR)in previously untreated patients with chronic lymphocytic leukemia(CLL). METHODS: The clinical data of 43 enrolled patients from May 2004 to December 2017 were analyzed the efficacy and survival results. RESULTS: A total of 43 patients with 31 males and 12 females, and the median age was 58 years old(range 36 to72)before treatment. There were 8 patients with symptom B. The median number of peripheral blood lymphocyte was 26(3–550)×10(9)/L. IGHV unmutated was detected in 62.1%(18/29)patients, P53 deletion in 14%(6/43)patients, RB1 deletion in 18.6%(8/43)patients, Trisomy 12 in 25.6%(11/33)patients, ATM deletion in 16.7%(7/42)patients, respectively. The median number of treatment courses administered was 4(range 2–6). Twenty patients obtained CR(46.5%), 18 patients obtained PR, 4 patients were SD, 1 patient was PD. The overall response rate(ORR)was 88.37%. Seven patients obtained MRD negative. After the median follow-up time of 51(6–167)months, median PFS was 67(29–105)months, median OS was not reach, 5-year PFS was(62.1±8.6)%, 10-year PFS was(31±14.3)%, 5-year OS was(70.5±8.3)%, and 10-year OS was(51.3±13.8)%. Less than 4 courses predicted adverse OS(P<0.05). P53 deletion and less than 4 courses were associated with poor PFS(P<0.001),and the prognostic value still remained after multivariate analysis[HR=7.65(95%CI 1.74–33.60), P=0.007; HR=3.75(95% CI 1.19–11.80), P=0.025]. Eighteen patients(41.9%)appeared grade 2–3 infection after chemotherapy, and 19 patients(44.2%)appeared grade 3–4 hematological adverse reactions. One patient(2.3%)was developed tumor lysis syndrome. All adverse reactions were controlled or recovered spontaneously. CONCLUSION: Previously untreated CLL patients treated with FCR had a high response rate and good survival rate, which is an important treatment choice for fit patients. Editorial office of Chinese Journal of Hematology 2021-07 /pmc/articles/PMC8408492/ /pubmed/34455740 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.07.003 Text en 2021年版权归中华医学会所有 https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 License.
spellingShingle 论著
氟达拉滨和环磷酰胺联合利妥昔单抗(FCR方案)一线治疗慢性淋巴细胞白血病43例临床分析
title 氟达拉滨和环磷酰胺联合利妥昔单抗(FCR方案)一线治疗慢性淋巴细胞白血病43例临床分析
title_full 氟达拉滨和环磷酰胺联合利妥昔单抗(FCR方案)一线治疗慢性淋巴细胞白血病43例临床分析
title_fullStr 氟达拉滨和环磷酰胺联合利妥昔单抗(FCR方案)一线治疗慢性淋巴细胞白血病43例临床分析
title_full_unstemmed 氟达拉滨和环磷酰胺联合利妥昔单抗(FCR方案)一线治疗慢性淋巴细胞白血病43例临床分析
title_short 氟达拉滨和环磷酰胺联合利妥昔单抗(FCR方案)一线治疗慢性淋巴细胞白血病43例临床分析
title_sort 氟达拉滨和环磷酰胺联合利妥昔单抗(fcr方案)一线治疗慢性淋巴细胞白血病43例临床分析
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408492/
https://www.ncbi.nlm.nih.gov/pubmed/34455740
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.07.003
work_keys_str_mv AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī
AT fúdálābīnhéhuánlínxiānànliánhélìtuǒxīdānkàngfcrfāngànyīxiànzhìliáomànxìnglínbāxìbāobáixuèbìng43lìlínchuángfēnxī