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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1217732 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type1 a. I* R2 r3 `  l7 M# J
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
" a. Y5 P9 Y1 [% D# w: D( @% ~+ Author Affiliations6 C4 }: a, f; y( d3 e
. g5 W7 h( E: K: U! D
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
8 s2 B3 E2 U; r  n' j2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan , ~8 U7 L* q- ~- |$ O" D: z
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan " J& W3 Z: m- ]
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
* y7 S% @: D0 U7 n) y4 L5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
$ [$ s7 R# ~! H: J4 U6 Z6 _6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan ! J: A$ ~5 G! Q  d
7Kinki University School of Medicine, Osaka 589-8511, Japan
' z' A# f) f/ c  v( i/ R/ ]0 X8 k8Izumi Municipal Hospital, Osaka 594-0071, Japan & C) ~# S* {' R
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan - d. ?% l( S7 r5 N2 v% x& |- m3 ]
Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp 8 z2 N, E! `2 s- t; u3 z
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. # N  y- q5 J7 O0 D6 P) A! ?- c
, U' J( [# R8 E5 e3 c7 w
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
6 f0 A! v3 @  ^" k8 Z' i. q# H6 k
, Y& C: {5 y& a8 \4 m; b0 F5 E5 ]Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato $ u8 X7 t4 {7 F3 w

0 S! _) Y7 u# X4 Q/ N/ F- E1 h4 T+ eAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  1 q; o/ }" r  R5 J. j9 H
6 M7 B2 A  C1 \& V7 e8 y5 ^" M6 z, _
Published online on: Thursday, December 1, 2011
* |( }2 h8 S1 Z9 y
9 u! M3 q& E* q# O! Z/ F! YDoi: 10.3892/ol.2011.507
, q! G, x- r* l7 r! ~+ z& ]
" G4 H+ M6 n$ @3 PPages: 405-410
+ b( b0 Z! a0 y1 F8 D- T! l4 @0 u9 n! h  m
Abstract:7 q- F8 b0 U; c! |3 \7 ]
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.4 U$ m, S) h7 M. Q% q) r( ?
( a3 v4 U* ^8 D; ?7 R8 l) f/ i
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
6 e$ D& v5 q9 m! q9 E( `2 M" d' VF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
9 K% d* X. |" r+ Author Affiliations
0 b5 j8 `- Y# c) T1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
2 [( e1 B; c2 P# E3 ~  j4 X. F  `2Department of Thoracic Surgery, Kyoto University, Kyoto . q1 w# m2 l6 J3 L( f' H
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
5 j$ s. x) X% S, E, P9 {7 l( M&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
& G2 z1 z; z8 c1 w3 qReceived September 3, 2010.
1 @$ ~; A" |+ e3 J- J) eRevision received November 11, 2010.
" a5 A. `& l3 A' uAccepted November 17, 2010.
; m0 L( V# L8 x% d& O# @2 aAbstract
4 [' D; e2 g+ J- \% ~* R- X# eBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. & r0 Y% E+ R6 c8 U) k
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
$ J, U* m: v$ k( y6 I! `Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
  A$ I- M7 K3 r% T4 R5 q. K( ~4 IConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
4 k# [5 b$ F# q2 g8 W今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?+ f" i) {. l# O5 a( U
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy; d/ p: d" [+ c# m0 z' u
http://clinicaltrials.gov/ct2/show/NCT01523587' N2 q7 k# c0 e, y; P1 U7 f
: \1 S  r: u. _
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
) j) r- e" S7 P8 S1 mhttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
; @  N9 d2 {/ ^: w5 @; P; M9 B. k; C
从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
1 Z5 n) d0 X9 F+ r* C至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
! M* w" r0 ]2 ]; `, G从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
; u# g( Z3 O5 ]: T( p9 m+ s至今为止,未出 ...

9 o) ]2 I2 L+ O7 P没有副作用是第一追求,效果显著是第二追求。
% l6 y2 Y5 ?- l* d" k/ H不错。

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