PMID- 33281065 OWN - NLM STAT- MEDLINE DCOM- 20211203 LR - 20211214 IS - 1938-0674 (Electronic) IS - 1533-0028 (Linking) VI - 20 IP - 2 DP - 2021 Jun TI - Occurrence and Management of Thrombocytopenia in Metastatic Colorectal Cancer Patients Receiving Chemotherapy: Secondary Analysis of Data From Prospective Clinical Trials. PG - 170-176 LID - S1533-0028(20)30142-0 [pii] LID - 10.1016/j.clcc.2020.10.004 [doi] AB - INTRODUCTION: Chemotherapy-induced thrombocytopenia (CIT) contributes to treatment dose delay and/or modification, often resulting in poorer survival and disease progression. We explored the incidence and clinical consequences of CIT among metastatic colorectal cancer (mCRC) patients. MATERIALS AND METHODS: Data from two prospective randomized phase 3 trials of mCRC patients receiving either first-line FOLFOX4 (fluorouracil, leucovorin, oxaliplatin) or second-line FOLFIRI (fluorouracil, leucovorin, irinotecan) were analyzed. Thrombocytopenia was defined by platelet count < 100 x 10(9)/L (further categorized by grade) and by recorded adverse events (AEs). Co-occurrence of anemia (hemoglobin < 12 g/dL) and neutropenia (neutrophil count < 2 x 10(9)/L) and clinical consequences of CIT were also evaluated. RESULTS: Among 1078 mCRC patients in the FOLFOX4 study, cumulative incidence of CIT based on platelet count was 37% (grade 3, 2%; grade 4, 1%) during an average 8 months' follow-up. Neutropenia or anemia were absent in 44% of CIT episodes; 62% of CIT AEs led to chemotherapy dose delay, change, and/or discontinuation. Among 1067 mCRC patients in the FOLFIRI study, cumulative incidence of CIT based on platelet count was 4% (grade 3, < 1%; grade 4, 0) during an average 4 months' follow-up. Neutropenia or anemia were absent in 22% of CIT episodes; 32% of CIT AEs led to chemotherapy dose delay, change, and/or discontinuation. With both regimens, transfusions and hospitalizations after CIT AEs were rare (< 3%). CONCLUSION: CIT was common among mCRC patients receiving the FOLFOX4 regimen. The most frequent consequence of CIT was a delay in chemotherapy, highlighting the unmet need in CIT management. CI - Copyright (c) 2020 The Authors. Published by Elsevier Inc. All rights reserved. FAU - Kilpatrick, Karynsa AU - Kilpatrick K AD - Amgen Inc, Thousand Oaks, CA. FAU - Shaw, Jaime L AU - Shaw JL AD - Amgen Inc, Thousand Oaks, CA. Electronic address: jshaw03@amgen.com. FAU - Jaramillo, Renee AU - Jaramillo R AD - SimulStat Inc, Solana Beach, CA. FAU - Toler, Andrew AU - Toler A AD - Amgen Inc, Thousand Oaks, CA. FAU - Eisen, Melissa AU - Eisen M AD - Amgen Inc, Thousand Oaks, CA. FAU - Sangare, Laura AU - Sangare L AD - SimulStat Inc, Solana Beach, CA. FAU - Soff, Gerald A AU - Soff GA AD - Hematology Service, Memorial Sloan-Kettering Cancer Center, New York, NY. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20201101 PL - United States TA - Clin Colorectal Cancer JT - Clinical colorectal cancer JID - 101120693 RN - 0 (Antineoplastic Agents) SB - IM MH - Aged MH - Anemia/chemically induced MH - Antineoplastic Agents/administration & dosage/*adverse effects MH - Antineoplastic Combined Chemotherapy Protocols/administration & dosage/*adverse effects MH - Colorectal Neoplasms/*drug therapy/pathology MH - Humans MH - Male MH - Middle Aged MH - Neoplasm Metastasis MH - Prospective Studies MH - Randomized Controlled Trials as Topic MH - Thrombocytopenia/*chemically induced/drug therapy OTO - NOTNLM OT - CIT OT - Chemotherapy dose delay OT - FOLFIRI OT - FOLFOX4 OT - mCRC EDAT- 2020/12/08 06:00 MHDA- 2021/12/15 06:00 CRDT- 2020/12/07 05:28 PHST- 2020/08/18 00:00 [received] PHST- 2020/10/07 00:00 [revised] PHST- 2020/10/26 00:00 [accepted] PHST- 2020/12/08 06:00 [pubmed] PHST- 2021/12/15 06:00 [medline] PHST- 2020/12/07 05:28 [entrez] AID - S1533-0028(20)30142-0 [pii] AID - 10.1016/j.clcc.2020.10.004 [doi] PST - ppublish SO - Clin Colorectal Cancer. 2021 Jun;20(2):170-176. doi: 10.1016/j.clcc.2020.10.004. Epub 2020 Nov 1.