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Erschienen in: Supportive Care in Cancer 6/2015

01.06.2015 | Original Article

Can grade 2 neutropenia predict the risk of grade 3 neutropenia in metastatic colorectal cancer patients treated with chemotherapy?

verfasst von: Yoichiro Yoshida, Seiichiro Hoshino, Naoya Aisu, Ai Mogi, Teppei Yamada, Daibo Kojima, Syu Tanimura, Keiji Hirata, Yuichi Yamashita

Erschienen in: Supportive Care in Cancer | Ausgabe 6/2015

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Abstract

Purpose

Neutropenia is a major factor affecting continuation of chemotherapy for colorectal cancer. In many clinical trials, a neutrophil count of >1500 is targeted for continuation; for a count of <1500, medication is commonly discontinued. However, there is no definitive evidence supporting the need for a neutrophil count of 1500 for continuation of chemotherapy. In the clinical trials that we conducted, we discontinued chemotherapy when the neutrophil count was <1000 (grade 3); for a count of 1000–1500 (grade 2), chemotherapy was continued. Therefore, even practical treatment uses the same setting. Our aim was to examine neutrophil counts during continuation of chemotherapy in colorectal cancer patients with counts of 1000–1500 and to assess the need for discontinuation of medication for neutrophil counts in this range. Moreover, we examined neutrophil counts during the previous course of chemotherapy when they fell below 1000.

Methods

The study included 144 patients who received XELOX + bevacizumab therapy and XELOX therapy for advanced or recurrent colorectal cancer.

Results

Thirty (20.8 %) patients had neutrophil counts of 1000–1500. One (3.3 %) of 30 patients had a neutrophil count of <1000 during the following course of chemotherapy. Moreover, among the patients with neutrophil counts of <1000, 27.3 % had counts of 1000–1500 during the previous course of chemotherapy and 72.7 % had counts of >1500.

Conclusions

Based on these results, grade 2 neutropenia cannot predict the risk of grade 3 neutropenia. Continuation of chemotherapy in patients with neutrophil counts of 1000–1500 may be appropriate, and discontinuation of therapy is not always required.
Literatur
1.
Zurück zum Zitat Network NCC (2010) NCCN clinical practice guidelines in oncology. Myeloid growth factors. v. 1.2010. NCCN Web site Network NCC (2010) NCCN clinical practice guidelines in oncology. Myeloid growth factors. v. 1.2010. NCCN Web site
2.
Zurück zum Zitat Lee SY, Kang HR, Song WJ, Lee KH, Han SW, Cho SH (2014) Overcoming oxaliplatin hypersensitivity: different strategies are needed according to the severity and previous exposure. Cancer Chemother Pharmacol 73(5):1021–1029CrossRefPubMed Lee SY, Kang HR, Song WJ, Lee KH, Han SW, Cho SH (2014) Overcoming oxaliplatin hypersensitivity: different strategies are needed according to the severity and previous exposure. Cancer Chemother Pharmacol 73(5):1021–1029CrossRefPubMed
3.
Zurück zum Zitat Crawford J, Dale DC, Lyman GH (2004) Chemotherapy‐induced neutropenia. Cancer 100(2):228–237CrossRefPubMed Crawford J, Dale DC, Lyman GH (2004) Chemotherapy‐induced neutropenia. Cancer 100(2):228–237CrossRefPubMed
4.
Zurück zum Zitat Kuderer NM, Dale DC, Crawford J, Cosler LE, Lyman GH (2006) Mortality, morbidity, and cost associated with febrile neutropenia in adult cancer patients. Cancer 106(10):2258–2266CrossRefPubMed Kuderer NM, Dale DC, Crawford J, Cosler LE, Lyman GH (2006) Mortality, morbidity, and cost associated with febrile neutropenia in adult cancer patients. Cancer 106(10):2258–2266CrossRefPubMed
5.
Zurück zum Zitat Bennouna J, Sastre J, Arnold D, Österlund P, Greil R, Van Cutsem E et al (2013) Continuation of bevacizumab after first progression in metastatic colorectal cancer (ML18147): a randomised phase 3 trial. Lancet Oncol 14(1):29–37CrossRefPubMed Bennouna J, Sastre J, Arnold D, Österlund P, Greil R, Van Cutsem E et al (2013) Continuation of bevacizumab after first progression in metastatic colorectal cancer (ML18147): a randomised phase 3 trial. Lancet Oncol 14(1):29–37CrossRefPubMed
6.
Zurück zum Zitat Rothenberg M, Cox J, Butts C, Navarro M, Bang Y-J, Goel R et al (2008) Capecitabine plus oxaliplatin (XELOX) versus 5-fluorouracil/folinic acid plus oxaliplatin (FOLFOX-4) as second-line therapy in metastatic colorectal cancer: a randomized phase III noninferiority study. Ann Oncol 19(10):1720–1726CrossRefPubMed Rothenberg M, Cox J, Butts C, Navarro M, Bang Y-J, Goel R et al (2008) Capecitabine plus oxaliplatin (XELOX) versus 5-fluorouracil/folinic acid plus oxaliplatin (FOLFOX-4) as second-line therapy in metastatic colorectal cancer: a randomized phase III noninferiority study. Ann Oncol 19(10):1720–1726CrossRefPubMed
7.
Zurück zum Zitat Sobrero A, Young S, Balcewicz M, Chiarra S, Perez Carrion R, Mainwaring P et al (2007) Phase IV study of first-line bevacizumab plus irinotecan and infusional 5-FU/LV in patients with metastatic colorectal cancer: AVIRI. J Clin Oncol : Off J Am Soc Clin Oncol 25:A4068 Sobrero A, Young S, Balcewicz M, Chiarra S, Perez Carrion R, Mainwaring P et al (2007) Phase IV study of first-line bevacizumab plus irinotecan and infusional 5-FU/LV in patients with metastatic colorectal cancer: AVIRI. J Clin Oncol : Off J Am Soc Clin Oncol 25:A4068
8.
Zurück zum Zitat Fisher GA, Kuo T, Ramsey M, Schwartz E, Rouse RV, Cho CD et al (2008) A phase II study of gefitinib, 5-fluorouracil, leucovorin, and oxaliplatin in previously untreated patients with metastatic colorectal cancer. Clin Cancer Res 14(21):7074–7079CrossRefPubMedCentralPubMed Fisher GA, Kuo T, Ramsey M, Schwartz E, Rouse RV, Cho CD et al (2008) A phase II study of gefitinib, 5-fluorouracil, leucovorin, and oxaliplatin in previously untreated patients with metastatic colorectal cancer. Clin Cancer Res 14(21):7074–7079CrossRefPubMedCentralPubMed
9.
Zurück zum Zitat Toffoli G, Cecchin E, Corona G, Russo A, Buonadonna A, D’Andrea M et al (2006) The role of UGT1A1* 28 polymorphism in the pharmacodynamics and pharmacokinetics of irinotecan in patients with metastatic colorectal cancer. J Clin Oncol 24(19):3061–3068CrossRefPubMed Toffoli G, Cecchin E, Corona G, Russo A, Buonadonna A, D’Andrea M et al (2006) The role of UGT1A1* 28 polymorphism in the pharmacodynamics and pharmacokinetics of irinotecan in patients with metastatic colorectal cancer. J Clin Oncol 24(19):3061–3068CrossRefPubMed
10.
Zurück zum Zitat Saltz LB, Meropol NJ, Loehrer PJ, Needle MN, Kopit J, Mayer RJ (2004) Phase II trial of cetuximab in patients with refractory colorectal cancer that expresses the epidermal growth factor receptor. J Clin Oncol 22(7):1201–1208CrossRefPubMed Saltz LB, Meropol NJ, Loehrer PJ, Needle MN, Kopit J, Mayer RJ (2004) Phase II trial of cetuximab in patients with refractory colorectal cancer that expresses the epidermal growth factor receptor. J Clin Oncol 22(7):1201–1208CrossRefPubMed
11.
Zurück zum Zitat Jeong J, Jeung H-C, Rha S, Im C, Shin S, Ahn J et al (2008) Phase II study of combination chemotherapy of 5-fluorouracil, low-dose leucovorin, and oxaliplatin (FLOX regimen) in pretreated advanced gastric cancer. Ann Oncol 19(6):1135–1140CrossRefPubMed Jeong J, Jeung H-C, Rha S, Im C, Shin S, Ahn J et al (2008) Phase II study of combination chemotherapy of 5-fluorouracil, low-dose leucovorin, and oxaliplatin (FLOX regimen) in pretreated advanced gastric cancer. Ann Oncol 19(6):1135–1140CrossRefPubMed
12.
Zurück zum Zitat Gruenberger B, Tamandl D, Schueller J, Scheithauer W, Zielinski C, Herbst F et al (2008) Bevacizumab, capecitabine, and oxaliplatin as neoadjuvant therapy for patients with potentially curable metastatic colorectal cancer. J Clin Oncol 26(11):1830–1835CrossRefPubMed Gruenberger B, Tamandl D, Schueller J, Scheithauer W, Zielinski C, Herbst F et al (2008) Bevacizumab, capecitabine, and oxaliplatin as neoadjuvant therapy for patients with potentially curable metastatic colorectal cancer. J Clin Oncol 26(11):1830–1835CrossRefPubMed
13.
Zurück zum Zitat Yoshida Y, Hoshino S, Aisu N, Naito M, Miyake T, Tanimura S et al (2013) Pilot study of the early start of chemotherapy after resection of primary colorectal cancer with distant metastases (Pearl Star 01). World J Surg Oncol 11(1):39CrossRefPubMedCentralPubMed Yoshida Y, Hoshino S, Aisu N, Naito M, Miyake T, Tanimura S et al (2013) Pilot study of the early start of chemotherapy after resection of primary colorectal cancer with distant metastases (Pearl Star 01). World J Surg Oncol 11(1):39CrossRefPubMedCentralPubMed
14.
Zurück zum Zitat Yoshida Y, Hasegawa J, Nezu R, Kim YK, Hirota M, Kawano K et al (2011) Clinical usefulness of mitochondrial transcription factor A expression as a predictive marker in colorectal cancer patients treated with FOLFOX. Cancer Sci 102(3):578–582CrossRefPubMed Yoshida Y, Hasegawa J, Nezu R, Kim YK, Hirota M, Kawano K et al (2011) Clinical usefulness of mitochondrial transcription factor A expression as a predictive marker in colorectal cancer patients treated with FOLFOX. Cancer Sci 102(3):578–582CrossRefPubMed
15.
Zurück zum Zitat Yoshida Y, Hoshino S, Aisu N, Shiwaku H, Beppu R, Tanimura S, et al. (2012) Dexamethasone as a means not only for controlling vascular pain caused by the administration of oxaliplatin via the peripheral vein but also for controlling oxaliplatin-induced hypersensitivity reactions. Br J Med Med Res 2(2):132–141 Yoshida Y, Hoshino S, Aisu N, Shiwaku H, Beppu R, Tanimura S, et al. (2012) Dexamethasone as a means not only for controlling vascular pain caused by the administration of oxaliplatin via the peripheral vein but also for controlling oxaliplatin-induced hypersensitivity reactions. Br J Med Med Res 2(2):132–141
16.
Zurück zum Zitat Yoshida Y, Hoshino S, Aisu N, Naito M, Tanimura S, Sasaki T et al (2014) Efficacy of XELOX plus bevacizumab in brain metastasis from rectal cancer. Case Rep Oncol 7(1):117–121CrossRefPubMedCentralPubMed Yoshida Y, Hoshino S, Aisu N, Naito M, Tanimura S, Sasaki T et al (2014) Efficacy of XELOX plus bevacizumab in brain metastasis from rectal cancer. Case Rep Oncol 7(1):117–121CrossRefPubMedCentralPubMed
17.
Zurück zum Zitat Yoshida Y, Hoshino S, Shiwaku H, Beppu R, Tanimura S, Tanaka S et al (2011) Early start of chemotherapy after resection of primary colon cancer with synchronous multiple liver metastases: a case report. Case Rep Oncol 4(2):250–254CrossRefPubMedCentralPubMed Yoshida Y, Hoshino S, Shiwaku H, Beppu R, Tanimura S, Tanaka S et al (2011) Early start of chemotherapy after resection of primary colon cancer with synchronous multiple liver metastases: a case report. Case Rep Oncol 4(2):250–254CrossRefPubMedCentralPubMed
18.
Zurück zum Zitat Yoshida Y, Hoshino S, Yamashita Y. Timing of initiation of chemotherapy after primary colorectal cancer resection. The Research and Biology of Cancer II, Edited by iConcept Press Ltd, 01/2014: chapter Timing of Initiation of Chemotherapy after Primary Colorectal Cancer Resection Yoshida Y, Hoshino S, Yamashita Y. Timing of initiation of chemotherapy after primary colorectal cancer resection. The Research and Biology of Cancer II, Edited by iConcept Press Ltd, 01/2014: chapter Timing of Initiation of Chemotherapy after Primary Colorectal Cancer Resection
19.
Zurück zum Zitat Yoshida Y, Hoshino S, Aisu N, Naito M, Tanimura S, Mogi A, et al. Administration of chemotherapy via the median cubital vein without implantable central venous access ports: port-free chemotherapy for metastatic colorectal cancer patients. International Journal of Clinical Oncology. 2014:1–6. doi:10.1007/s10147-014-0703-5 Yoshida Y, Hoshino S, Aisu N, Naito M, Tanimura S, Mogi A, et al. Administration of chemotherapy via the median cubital vein without implantable central venous access ports: port-free chemotherapy for metastatic colorectal cancer patients. International Journal of Clinical Oncology. 2014:1–6. doi:10.​1007/​s10147-014-0703-5
20.
Zurück zum Zitat Lyman GH, Dale DC, Crawford J (2003) Incidence and predictors of low dose-intensity in adjuvant breast cancer chemotherapy: a nationwide study of community practices. J Clin Oncol 21(24):4524–4531CrossRefPubMed Lyman GH, Dale DC, Crawford J (2003) Incidence and predictors of low dose-intensity in adjuvant breast cancer chemotherapy: a nationwide study of community practices. J Clin Oncol 21(24):4524–4531CrossRefPubMed
21.
Zurück zum Zitat Wood WC, Budman DR, Korzun AH, Cooper MR, Younger J, Hart RD et al (1994) Dose and dose intensity of adjuvant chemotherapy for stage II, node-positive breast carcinoma. N Engl J Med 330(18):1253–1259CrossRefPubMed Wood WC, Budman DR, Korzun AH, Cooper MR, Younger J, Hart RD et al (1994) Dose and dose intensity of adjuvant chemotherapy for stage II, node-positive breast carcinoma. N Engl J Med 330(18):1253–1259CrossRefPubMed
22.
Zurück zum Zitat Hochster H, Hart L, Ramanathan R, Hainsworth J, Hedrick E, Childs B (2006) Safety and efficacy of oxaliplatin/fluoropyrimidine regimens with or without bevacizumab as first-line treatment of metastatic colorectal cancer (mCRC): final analysis of the TREE-study. J Clin Oncol : Off J Am Soc Clin Oncol 24(18S):3510 Hochster H, Hart L, Ramanathan R, Hainsworth J, Hedrick E, Childs B (2006) Safety and efficacy of oxaliplatin/fluoropyrimidine regimens with or without bevacizumab as first-line treatment of metastatic colorectal cancer (mCRC): final analysis of the TREE-study. J Clin Oncol : Off J Am Soc Clin Oncol 24(18S):3510
23.
Zurück zum Zitat Cassidy J, Clarke S, Díaz-Rubio E, Scheithauer W, Figer A, Wong R et al (2008) Randomized phase III study of capecitabine plus oxaliplatin compared with fluorouracil/folinic acid plus oxaliplatin as first-line therapy for metastatic colorectal cancer. J Clin Oncol 26(12):2006–2012CrossRefPubMed Cassidy J, Clarke S, Díaz-Rubio E, Scheithauer W, Figer A, Wong R et al (2008) Randomized phase III study of capecitabine plus oxaliplatin compared with fluorouracil/folinic acid plus oxaliplatin as first-line therapy for metastatic colorectal cancer. J Clin Oncol 26(12):2006–2012CrossRefPubMed
24.
Zurück zum Zitat Ducreux M, Bennouna J, Hebbar M, Ychou M, Lledo G, Conroy T et al (2011) Capecitabine plus oxaliplatin (XELOX) versus 5‐fluorouracil/leucovorin plus oxaliplatin (FOLFOX‐6) as first‐line treatment for metastatic colorectal cancer. Int J Cancer 128(3):682–690CrossRefPubMed Ducreux M, Bennouna J, Hebbar M, Ychou M, Lledo G, Conroy T et al (2011) Capecitabine plus oxaliplatin (XELOX) versus 5‐fluorouracil/leucovorin plus oxaliplatin (FOLFOX‐6) as first‐line treatment for metastatic colorectal cancer. Int J Cancer 128(3):682–690CrossRefPubMed
25.
Zurück zum Zitat Aapro MS, Cameron DA, Pettengell R, Bohlius J, Crawford J, Ellis M et al (2006) EORTC guidelines for the use of granulocyte-colony stimulating factor to reduce the incidence of chemotherapy-induced febrile neutropenia in adult patients with lymphomas and solid tumours. Eur J Cancer 42(15):2433–2453CrossRefPubMed Aapro MS, Cameron DA, Pettengell R, Bohlius J, Crawford J, Ellis M et al (2006) EORTC guidelines for the use of granulocyte-colony stimulating factor to reduce the incidence of chemotherapy-induced febrile neutropenia in adult patients with lymphomas and solid tumours. Eur J Cancer 42(15):2433–2453CrossRefPubMed
Metadaten
Titel
Can grade 2 neutropenia predict the risk of grade 3 neutropenia in metastatic colorectal cancer patients treated with chemotherapy?
verfasst von
Yoichiro Yoshida
Seiichiro Hoshino
Naoya Aisu
Ai Mogi
Teppei Yamada
Daibo Kojima
Syu Tanimura
Keiji Hirata
Yuichi Yamashita
Publikationsdatum
01.06.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
Supportive Care in Cancer / Ausgabe 6/2015
Print ISSN: 0941-4355
Elektronische ISSN: 1433-7339
DOI
https://doi.org/10.1007/s00520-014-2518-3

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