University of Turin, Medical Oncology Department, Institute for Cancer Research and Treatment, Candiolo, Italy.
Cancer. 2013 Jan 15;119(2):277-84. doi: 10.1002/cncr.27736. Epub 2012 Jul 6.
Chemoradiotherapy (CRT) may render curative resection feasible in patients with locally advanced pancreatic carcinoma (LAPC). The authors previously demonstrated the achievement of significant disease control and a median survival of 14 months by CRT in patients with LAPC. In this study, they evaluated the use of induction chemotherapy followed by a CRT neoadjuvant protocol.
Patients first received induction gemcitabine and oxaliplatin (GEMOX) (gemcitabine 1000 mg/m(2), oxaliplatin 100 mg/m(2)). Patients without disease progression then received gemcitabine twice weekly (50 mg/m(2) daily) concurrent with radiotherapy (50.4 grays) and were re-evaluated for resectability.
Thirty-nine patients (15 with borderline resectable disease and 24 with unresectable disease) entered the study. The treatment was well tolerated. Disease control was obtained in 29 of 39 patients. Two patients progressed after GEMOX, and 7 progressed after CRT. After a median follow-up of 13 months, the median progression-free survival (PFS) was 10.2 months. The median PFS of patients with borderline resectable and unresectable disease was 16.6 and 9.1 months, respectively (P = .056). For the whole group, the median overall survival (OS) was 16.7 months (27.8 months for patients with borderline resectable disease, 13.3 for patients with unresectable disease; P = .045). Eleven patients (9 with borderline resectable disease and 2 with unresectable disease at diagnosis) underwent successful resection. Patients who underwent resection had a significantly longer median PFS compared with nonresected patients (19.7 months vs 7.6 months, respectively). The median OS among resected and nonresected patients was 31.5 months and 12.3 months, respectively (P < .001).
The current results indicated that induction GEMOX followed by CRT is feasible in patients with LAPC. Both those with borderline resectable disease and those with unresectable disease received clinical benefit, a chance to obtain resectability, and improved survival. The authors concluded that this protocol warrants further evaluation.
放化疗(CRT)可能使局部晚期胰腺癌(LAPC)患者的根治性切除成为可能。作者之前证明了 CRT 可使 LAPC 患者获得显著的疾病控制和 14 个月的中位生存期。在这项研究中,他们评估了诱导化疗加 CRT 新辅助方案的应用。
患者首先接受诱导吉西他滨和奥沙利铂(GEMOX)(吉西他滨 1000mg/m²,奥沙利铂 100mg/m²)。无疾病进展的患者随后每周接受两次吉西他滨(50mg/m²,每日一次),同时接受放射治疗(50.4 格雷),并重新评估可切除性。
39 例患者(15 例为交界可切除性疾病,24 例为不可切除性疾病)入组研究。治疗耐受性良好。39 例患者中有 29 例获得疾病控制。2 例患者在 GEMOX 后进展,7 例患者在 CRT 后进展。中位随访 13 个月后,中位无进展生存期(PFS)为 10.2 个月。交界可切除性和不可切除性疾病患者的中位 PFS 分别为 16.6 个月和 9.1 个月(P=0.056)。对于整个研究组,中位总生存期(OS)为 16.7 个月(交界可切除性疾病患者为 27.8 个月,不可切除性疾病患者为 13.3 个月;P=0.045)。11 例患者(9 例为交界可切除性疾病,2 例为不可切除性疾病)成功接受了手术切除。与未行切除术的患者相比,接受切除术的患者中位 PFS 显著延长(分别为 19.7 个月和 7.6 个月)。行切除术和未行切除术患者的中位 OS 分别为 31.5 个月和 12.3 个月(P<0.001)。
目前的结果表明,LAPC 患者接受诱导 GEMOX 后加 CRT 是可行的。交界可切除性疾病和不可切除性疾病患者均获得临床获益、获得可切除性的机会和改善的生存。作者认为该方案值得进一步评估。