Tolaney Sara M, Najita Julie, Winer Eric P, Burstein Harold J
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Clin Breast Cancer. 2008 Aug;8(4):352-6. doi: 10.3816/CBC.2008.n.041.
We observed 2 cases of Pneumocystis carinii pneumonia (PCP) occurring in HIV-negative patients during treatment with dose-dense chemotherapy with doxorubicin/cyclophosphamide (AC) followed by paclitaxel (T). These represent the first case reports of PCP occurring during dose-dense chemotherapy for breast cancer. Because lymphocyte depletion is thought to predispose patients to PCP, we explored whether the shortened intervals between cycles during dose-dense chemotherapy might place patients at risk for lymphocyte depletion and thereby a potentially increased risk of opportunistic infection.
Three cohorts of patients were analyzed. Cohort 1 involved 135 patients receiving dose-dense AC --> T on a phase II study. Cohort 2 included 64 patients who received treatment with dose-dense AC --> albumin-bound paclitaxel on a phase II clinical trial. Cohort 3 consisted of 59 patients who received AC --> T given every 3 weeks who were identified from the Clinical Research Information System database at Dana-Farber Cancer Institute. For cohorts 1 and 3, the electronic medical record was reviewed to determine absolute lymphocyte counts (ALCs) and absolute neutrophil counts (ANCs) for day 1 of each of the 8 cycles of treatment. For cohort 2, data was prospectively collected and entered into an electronic database. The lowest ALC obtained by each patient on day 1 of any cycle was termed the nadir.
Patients experienced grade 3 (ALC < 500 cells/mm3) or grade 4 (ALC < 200 cells/mm3) lymphopenia in all 3 cohorts: 63% with dose-dense AC -->T, 23.4% in dosedense AC --> albumin-bound paclitaxel, and 69% with dose-dense AC --> T every 3 weeks. Patients experienced their lowest median ALC count at cycle 5 of treatment in all 3 cohorts, with a median nadir of 400 cells/mm3 in cohort 1, 690 cells/mm3 in cohort 2, and 400 cells/mm3 in cohort 3.
The majority of patients receiving AC --> T every 2 or 3 weeks experience grade 3/4 lymphopenia. Median lymphocyte counts appear to be lowest around cycle 5, the point at which we observed 2 cases of PCP. Lymphocyte counts appear to be reaching a low enough level to place patients at risk for opportunistic infection during treatment with dosedense AC --> T and with AC --> T given every 3 weeks.
我们观察到2例卡氏肺孢子虫肺炎(PCP)发生在接受阿霉素/环磷酰胺(AC)剂量密集化疗后序贯紫杉醇(T)治疗的HIV阴性患者中。这些是乳腺癌剂量密集化疗期间发生PCP的首例病例报告。由于淋巴细胞减少被认为会使患者易患PCP,我们探讨了剂量密集化疗期间缩短周期间隔是否会使患者有淋巴细胞减少的风险,从而有机会性感染风险增加的可能性。
分析了三组患者。第一组包括135例在一项II期研究中接受剂量密集AC→T治疗的患者。第二组包括64例在一项II期临床试验中接受剂量密集AC→白蛋白结合型紫杉醇治疗的患者。第三组由59例每3周接受AC→T治疗的患者组成,这些患者是从达纳-法伯癌症研究所的临床研究信息系统数据库中识别出来的。对于第一组和第三组,查阅电子病历以确定治疗的8个周期中每个周期第1天的绝对淋巴细胞计数(ALC)和绝对中性粒细胞计数(ANC)。对于第二组,前瞻性收集数据并录入电子数据库。每位患者在任何周期第1天获得的最低ALC被称为最低点。
所有三组患者均出现3级(ALC<500个细胞/mm³)或4级(ALC<200个细胞/mm³)淋巴细胞减少:接受剂量密集AC→T的患者中有63%,接受剂量密集AC→白蛋白结合型紫杉醇的患者中有23.4%,每3周接受剂量密集AC→T的患者中有69%。所有三组患者在治疗第5周期时出现最低中位数ALC计数,第一组最低点中位数为400个细胞/mm³,第二组为690个细胞/mm³,第三组为400个细胞/mm³。
每2或3周接受AC→T治疗的大多数患者出现3/4级淋巴细胞减少。淋巴细胞计数中位数似乎在第5周期左右最低,我们在此观察到2例PCP病例。在剂量密集AC→T治疗以及每3周接受AC→T治疗期间,淋巴细胞计数似乎降至足够低的水平,使患者有机会性感染的风险。