Nuova speranza per i pazienti con cancro gastrico localmente avanzato

Condividi questo post

Cancro gastrico avanzato

Gastric cancer has long been in the lead in terms of morbidity and mortality of malignant digestive tract tumors. The biggest reason is that once it is found to be in advanced stages, the prognosis is poor. Even in Europe and North America, the 5-year survival rate for T3 / T4 gastric cancer is only 20%. How to improve the survival of patients is a difficult problem before clinical tumor treatment.

In the field of medical treatment, perioperative chemotherapy or neoadjuvant chemotherapy has been applied to gastric cancer and adenocarcinoma of the gastroesophageal junction, and neoadjuvant radiochemotherapy is also widely used in esophageal cancer. Perioperative chemotherapy options include epirubicin + cisplatin + fluorouracil (ECF) used in the MAGIC study, and cisplatin + fluorouracil used in the FNCLCC / FFCD 9703 study.Despite some achievements, the exploration of adjuvant therapy for gastric cancer during the perioperative period is still long. In terms of drug selection, anthracycline combined with fluorouracil and platinum programs have been verified, but there is little research on whether docetaxel can play a therapeutic role under new auxiliary conditions.For advanced metastatic gastric cancer, first-line or second-line treatment of docetaxel has proved effective, including FLOT (fluorouracil + calcium folinate + oxaliplatin + docetaxel) 2-week regimen. In the neoadjuvant study of gastric cancer, the FLOT scheme compared with the ECX (epirubicin + cisplatin + capecitabine) scheme, the pathological complete remission rate is higher.Therefore, the researchers conducted a FLOT4 phase II / III study to compare the efficacy of the ECF / ECX scheme and the FLOT scheme in the perioperative treatment of resectable adenocarcinoma of the gastric / gastroesophageal junction. Recently, the results of Phase II of the FLOT4 study were published online in the journal Lancet Oncology.

Ricerca principale

FLOT4 is an open-label, randomized, ontrolled Ⅱ / Ⅲ study. The patients come from 28 tumor centers in Germany. They require resectable adenocarcinoma of the stomach or gastroesophageal junction. The clinical stage is cT2 or higher. 0-2. Patients were randomly assigned to the ECF / ECX treatment group (three cycles before and after surgery) or the FLOT treatment group (four cycles before and after surgery) at a 1: 1 ratio. According to ECOG PS, the primary tumor site, age, and lymph node status stratify patients.
 
The primary endpoint was complete pathological remission (TRG1a, tumor regression grade). The study (including the phase III part) has been completed for enrollment, and this is a mid-term analysis.
 
From August 2010 to August 2012, 300 patients with gastric cancer were enrolled in the Phase II study, including 152 in the ECF / ECX group and 148 in the FLOT group. Based on the revised definition of intention-to-treat population, a total of 265 cases can be evaluated (ECF / ECX = 137, FLOT = 128).

Main results

The perioperative treatment completion rates of FLOT and ECX / ECF treatment groups were 93% (119) and 92% (126), respectively.The pathological complete remission rate of patients in the FLOT treatment group was higher than that of ECX / ECF, respectively 16% (20/128) vs 6% (8/137).In terms of safety, the incidence of at least one surgical complication or perioperative serious adverse event was 25% (30/119) in the FLOT group and 40% (44/111) in the ECX / ECF group.The most common non-surgical grade 3-4 adverse events in the two treatment groups were neutropenia (38% [ECX / ECF] vs 52% [FLOT]), leukopenia (20% vs 28%), and nausea (17 % vs 9%), infection (12% vs 12%), fatigue (14% vs 9%) and vomiting (10% vs 3%).

Conclusione

The perioperative FLOT program has anti-tumor activity and is easy to implement. It may become a treatment option for locally advanced resectable adenocarcinoma of the stomach or gastroesophageal junction.

However, whether this result can be truly applied to clinical practice requires caution. First, can pathological complete remission as the primary endpoint translate into patient survival benefit? At present, there is no definite evidence for improvement in overall survival or progression-free survival in Phase II studies, and the final results will have to wait for Phase III studies.

In addition, the pathological complete response rate of perioperative chemotherapy is usually not more than 10% (close to 3%), and the pCR rate of 16% of the FLOT scheme may be abnormal. As for the FLOT regimen itself, whether 4 cycles are appropriate is still unclear, and the potential toxicity of the combined treatment of three cytotoxic drugs is worrying. When cytotoxic chemotherapy has entered the bottleneck during the perioperative period, the treatment plan should give room for new immunotherapy or targeted therapy.

The exploration of perioperative adjuvant therapy for locally advanced gastric cancer will continue. Radiotherapy combined with chemotherapy or individualized treatment based on molecular classification of gastric cancer are all directions.

Iscriviti alla nostra Newsletter

Ricevi aggiornamenti e non perdere mai un blog da Cancerfax

Altro da esplorare

Terapia con cellule CAR T di origine umana: scoperte e sfide
Terapia con cellule T CAR

Terapia con cellule CAR T di origine umana: scoperte e sfide

La terapia con cellule CAR T basate sull’uomo rivoluziona il trattamento del cancro modificando geneticamente le cellule immunitarie del paziente per colpire e distruggere le cellule tumorali. Sfruttando la potenza del sistema immunitario del corpo, queste terapie offrono trattamenti potenti e personalizzati con il potenziale per una remissione duratura in vari tipi di cancro.

Comprensione della sindrome da rilascio di citochine: cause, sintomi e trattamento
Terapia con cellule T CAR

Comprensione della sindrome da rilascio di citochine: cause, sintomi e trattamento

La sindrome da rilascio di citochine (CRS) è una reazione del sistema immunitario spesso innescata da alcuni trattamenti come l’immunoterapia o la terapia con cellule CAR-T. Implica un rilascio eccessivo di citochine, causando sintomi che vanno dalla febbre e affaticamento a complicazioni potenzialmente pericolose per la vita come danni agli organi. La gestione richiede un attento monitoraggio e strategie di intervento.

Ho bisogno di aiuto? Il nostro team è pronto ad assisterti.

Auguriamo una pronta guarigione del tuo caro e vicino.

inizia chat
Siamo in linea! Chatta con noi!
Scansiona il codice
Ciao,

Benvenuti in CancerFax!

CancerFax è una piattaforma pionieristica dedicata a connettere individui affetti da cancro in stadio avanzato con terapie cellulari rivoluzionarie come la terapia CAR T-Cell, la terapia TIL e studi clinici in tutto il mondo.

Ci faccia sapere che cosa possiamo fare per lei.

1) Cure contro il cancro all'estero?
2) Terapia CAR T-Cell
3) Vaccino contro il cancro
4) Consultazione video online
5) Terapia protonica