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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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1174721 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 Type
# [. q9 B2 g& v7 m4 x$ k0 HNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9   C! X- O8 N. J" ?& F' O# s& q) d9 u
+ Author Affiliations
1 H+ [1 N) O2 r/ Y. f0 n
% b( j7 z7 H( [' X4 {' K1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan / f& Z3 X0 E5 R3 i- N$ ~% B( j/ M: \
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
& c2 y  l* q: K2 i% K% B3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
' F# @1 ^: }" s# h# O6 r4 _4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
, o, [0 x9 v* Q( e" z/ v" p5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
( \: Q, @* B" V& J6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan % o/ {4 K' O! X
7Kinki University School of Medicine, Osaka 589-8511, Japan # o* _) `! \) E5 I8 G# _1 q
8Izumi Municipal Hospital, Osaka 594-0071, Japan
/ x0 ]1 o4 G) P+ n$ d# J% i9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
. B9 f4 i4 t  Q6 l+ Y! uCorrespondence 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 / O6 n8 y/ u/ z) |3 G7 k8 O- G% M
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. 5 {% n' J" z+ b+ U( s) \; y

4 A' ?* S6 W/ Z; V! Y  ]
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 9 V+ H* a+ U0 I7 f
! i8 H  o5 j( X2 h% H
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato & b. H* C; b& c% C

9 V& E" c+ ]3 W0 {9 mAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  : J$ h' K. \+ e

+ J3 r- L0 Y( h. nPublished online on: Thursday, December 1, 2011 3 J+ ^3 V$ `; u$ U' V+ B( T1 ^

3 L* n$ O% w- u* ZDoi: 10.3892/ol.2011.507 + B3 T4 ?1 u+ d6 y; r: m

2 N% D5 s- L3 B  s" WPages: 405-410
* T' ^: P8 O+ y9 [0 r2 s# @% C: a$ h9 u* }: z' F0 }
Abstract:
, _0 `2 P. @- dS-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., c( G1 p5 c. T  l; S- ^9 I4 C7 [3 f
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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 population5 v$ V! ^! S- u5 q( v0 ^8 H- r
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 & j& c! R" q, {7 N% p, ~( J
+ Author Affiliations
9 S( y5 [2 {# ]1 E1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
' Q* ?/ y) ~# S% I+ G5 o7 ]2Department of Thoracic Surgery, Kyoto University, Kyoto ! [& ]. K! t0 q8 g8 m
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
8 T. F: }2 `+ [$ N0 L* h&#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 # Y7 D$ S8 E" j0 s! I  {$ w  t8 K
Received September 3, 2010.
3 U" P# ^. q/ w4 Z% P# b, ]! gRevision received November 11, 2010.
. Y! Q- Y! U5 S" x" \# I, dAccepted November 17, 2010.
9 h0 Y1 l& c2 A3 S5 f+ J  FAbstract
9 k$ |& w8 O% ~Background: 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.
# \& S  D$ J0 w* j, [' t! W& T- APatients 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. : @# s! I: ^' B) A3 U( \
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.
- B- V7 c1 S6 K; E. h* S3 VConclusion: 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。$ z# H, Z0 [! M$ p+ A% H) H, _- A
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?9 U$ g' s* E% d/ N" _
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
  L1 {7 \  _0 U) \/ Qhttp://clinicaltrials.gov/ct2/show/NCT01523587" X& A2 m5 ?! Q

1 G2 h9 O, N. r4 B. w, BBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
# Y: U9 h. `4 G& qhttp://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 & \& g' D! I0 E2 E; y% l+ i

9 s  q+ X. _! C* ]: Z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。' d0 O% d0 ~; _9 T% [% }( f
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
$ N7 u) X' I# e+ O6 L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。
) v5 ^1 V3 p% E2 h& q' V, T5 i至今为止,未出 ...

, g: M& v9 m7 H' i: Y没有副作用是第一追求,效果显著是第二追求。7 J& f  T, Y8 R
不错。

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